Cyanobacteria: A Precious Bio-resource in Agriculture, Ecosystem, and Environmental Sustainability.

Keeping in view, the challenges concerning agro-ecosystem and environment, the recent developments in biotechnology offers a more reliable approach to address the food security for future generations and also resolve the complex environmental problems. Several unique features of cyanobacteria such as oxygenic photosynthesis, high biomass yield, growth on non-arable lands and a wide variety of water sources (contaminated and polluted waters), generation of useful by-products and bio-fuels, enhancing the soil fertility and reducing green house gas emissions, have collectively offered these bio-agents as the precious bio-resource for sustainable development. Cyanobacterial biomass is the effective bio-fertilizer source to improve soil physico-chemical characteristics such as water-holding capacity and mineral nutrient status of the degraded lands. The unique characteristics of cyanobacteria include their ubiquity presence, short generation time and capability to fix the atmospheric N2. Similar to other prokaryotic bacteria, the cyanobacteria are increasingly applied as bio-inoculants for improving soil fertility and environmental quality. Genetically engineered cyanobacteria have been devised with the novel genes for the production of a number of bio-fuels such as bio-diesel, bio-hydrogen, bio-methane, synga, and therefore, open new avenues for the generation of bio-fuels in the economically sustainable manner. This review is an effort to enlist the valuable information about the qualities of cyanobacteria and their potential role in solving the agricultural and environmental problems for the future welfare of the planet.

Introduction

The present world populatiopan class="Chemical">n of about 7.2 billion is expected to cross 9.6 billion by the end of year 2050. In order to provide food to all by that times, the annual production of cereals needs a jump of about 50%, i.e., from 2.1 billion tons per year to ∼3 billion tons per year. This onerous target puts enormous pressure on agriculture sector to achieve the food security. But such a quantum leap in food production can be achieved either by bringing more and more land under cultivation or by enhancing the productivity of cultivable land available. The first option remains a distant dream in the light of limited land and growing population. The option of increasing sn class="Chemical">oil fertility and agricultural productivity with the help of better eco-friendly management tools, promises a successful food security.

The current agricultural practices are heavily depepan class="Chemical">ndent on the application of synthetic fertilizers and pesticides, intensive tillage, and over irrigation, which have undoubtedly helped many developing countries to meet the food requirement of their people; nevertheless raised environmental and health problems, which include deterioration of soil fertility, overuse of land and water resources, polluted environment, and increased cost of agricultural production. A big question before the present day agriculture is to enhance the agricultural production to meet the present and future food requirements of the population within the available limited resources, without deteriorating the environmental quality (Singh and Strong, 2016). The sustainable agriculture practices can fulfill the growing need of food as well as environmental quality (Mason, 2003). The present philosophy of sustainable agriculture includes eco-friendly, low-cost farming with the help of native microorganisms. It also emphasizes that the farmers should work with natural processes to conserve resource such as soil and water, whilst minimizing the cost of agricultural production and waste generation that adversely affects the environment quality. Such sustainable agricultural management practices will make the agro-ecosystem more resilient, self-regulating and also maintain the productivity and profitability.

Since lopan class="Chemical">ng, the microbes have been known to contribute to the soil fertility and sustainable green energy production (Koller et al., 2012). Durinpan>g the last decades, the microbial processes of green energy production have gained interest as the sustainable tool for the generation of bio-fuels, namely methane (CH4), ethanol, H2, butanol, syngas, etc. Current investigations witnessed noteworthy surge growth in the production of cyanobacterial biomass for bio-fuels, food supplements (super foods), and bio-fertilizers for safe agriculture (Yamaguchi, 1997; Benson et al., 2014). They have been classified as beneficial as well as harmless bio-agents based on their role in regulating plant productivity. In reality, these two diverse groups of microorganisms coexist in nature, and predominance of one at any point of time, depends mainly on the environmental conditions. For many years, soil microbiologists and microbial ecologists have been studying the effect of beneficial or efficient soil microorganisms for sustainable agriculture which not only contribute to soil fertility, crop growth and yield, but also improve the environment quality.

n class="Chemical">Npan>owadays, sustainable agriculture practices have envisaged an important role of these tiny microorganisms in achieving the food security without creating environmental problems. The recent trends of using the bio-inoculants containing beneficial soil microbes over synthetic fertilizers, insecticides, and pesticides for enhancing crop productivity is a welcome step. As a beneficial microbe, cyanobacteria could play a potential role in the enhancement of agriculture productivity and mitigation of GHG emissions (Singh, 2011; Singh et al., 2011a). Very recently, it has been proposed that cyanobacteria could be the vital bio-agents in ecological restoration of degraded lands (Singh, 2014). Cyanobacteria are the group of photosynthetic organisms which can easily survive on bare minimum requirement of light, carbon dioxide (CO2) and water (Woese, 1987; Castenholz, 2001). They are phototrophic, and naturally occur in several agro-ecosystems like paddy fields and from Antarctica to Arctic poles (Pandey et al., 2004). They fulfill their own nitrogen requirement by nitrogen (N2)-fixation, and produce some bioactive compounds, which promote the crop growth/protect them from pathogens and improve the soil nutrient status. Cyanobacteria are also useful for wastewater treatment, and have the ability to degrade the various toxic compounds even the pesticides (Cohen, 2006). A conceptual model about the role of cyanobacteria in sustainable agriculture and environmental management has been proposed (Figure ). This review highlights the role of cyanobacteria in bio-energy production, ecological restoration, agriculture and environmental sustainability.

A hypothetical model exhibiting the potential roles of cyanobacteria in sustainable agriculture and environmental management.

Methods

The reviews by the authors covered the valuable role of cyanobacteria ipan class="Chemical">n development of sustainable agriculture and environment is described in Figures and , with different approaches proposed. In this article, the present viewpoint of sustainable agriculture and environment includes eco-friendly, low-cost farming with the help of bio-agents like cyanobacteria based on specific, internally reliable hypothesis and values. The various approaches proposed in Figures demonstrate that cyanobacteria are the effective tool for enhancing the sn class="Chemical">oil fertility, bio-fuel production, bioremediation, reducing GHGs emissions, and enhancing crop productivity. Finally, it was proposed that the genetically engineered cyanobacteria can be exploited as the multi-functional bio-agents for eco-friendly agriculture and other beneficial uses for sustainable development (Tables ).

A model showing the technologies used for production of bio-fuels from the mass cultivation of cyanobacteria.

Production of bio-fuels from genetically modified cyanobacteria (data has been modified from .

Important n class="Chemical">nitrogen fixing cyanobacterial genpan>era.

Heavy n class="Chemical">metal removal by some cyanobacterial species.

Some cyanobacterial members and their n class="Chemical">lipid contents (modified from Sharathchandra and Rajashekhar, 2011).

n class="Chemical">Bio-methane producing cyanobacterial members.

Cyanobacteria in Sustainable Management

Beneficial microbes are apan class="Chemical">n alternative to other management practices. The cyanobacteria are bestowed with ability to fix atmospheric N2, decompose the organic wastes and residues, detoxify heavy metals, pesticides, and other xenobiotics, catalyze the nutrient cycling, suppress growth of pathogenic microorganisms in soil and water, and also produce some bioactive compounds such as vitamins, hormones, and enzymes which contribute to plant growth (Higa, 1991). These bio-agents can improve the soil quality and plant growth, and minimize the crop production cost by supplementing the good crop management practices such as crop rotation, use of organic manures, minimum tillage, and the bio-control of pests and diseases. The use of cyanobacteria in agriculture promises definite beneficial effects on crop productivity, if used properly (Higa and Wididana, 1991).

The currently used traditional agriculture management practices heavily rely on the application of chemical fertilizers and pesticides, and practices like intensive tillage and excess irrigation which otherwise lead to ever increasing cost of agricultural production, over exploitation of natural resources like soil and water, and also create environmental pollution (Kumar et al., 2012). Now, there is need to adopt such sustainable agricultural practices which are not only eco-friendly, but are also cost-effective, and really help us attain the long-term food security. Some of the major objectives of sustainable agriculture include production of safe and healthy foods, conservation of natural resources, economic viability, restoration and conservation of ecosystem services. An eco-friendly management approach for complex agro-ecosystem without disturbing the interactions among number of ecological components like water, edaphic and climatic factors including the living components offers the long-term rise for sustainable increase in productivity. It may be suggested that if the four major ecosystems processes, i.e., energy flow, water cycle, mineral cycles, and ecosystem dynamics, function together without disturbing the harmony or homeostasis of individual components, can ultimately reduce the cost of agriculture production.

The application of cyapan class="Chemical">nobacteria in management of soil and environment inpan>cludes the economic benefits (reduced input cost), nutrient cycling, N2-fixation, bioavailability of phosphorus, water storage and movement, environmental protection and prevention of pollution and land degradation especially through reducing the use of agro-chemicals, and recycling of nutrients and restoration of soil fertility through reclamation (Shukia et al., 2008).

The following benefits to the agro-ecosystem are offered through use of cyanobacteria:

Enhanced solubilization and mobility of nutrients of limited supply.

Complexing of heavy n class="Chemical">metals anclass="Chemical">pan>d xenobiotics to limit their mobility and transport inpan> plants.

Mineralization of simpler organic molecules such as amino acids for direct uptake.

Protection of plants from pathogenic insects and diseases as bio-control agents.

Stimulation of the plapan class="Chemical">nt growth due to their plant growth promoting attributes.

Improving the physico-chemical conditions of sn class="Chemical">oils.

Cyanobacteria under Extreme Environments

Cyanobacteria commopan class="Chemical">nly known as blue-green-algae, are not truly eukaryotic algae. They are Gram-negative prokaryotes, perform oxygenic photosynthesis, and also fix atmospheric N2. They are ubiquitous in ponds, lakes, water streams, rivers, and wetlands. They can easily survive the extreme environments such as hot springs, hyper-saline waters, freezing environments, and arid deserts (Singh, 2014). Cyanobacteria are able to survive at a temperature range of 45–70°C (Castenholz, 1978) and pH lower than 4–5 (Pfennig, 1969, 1974) with optimum range of 7.5–10 (Fogg, 1956). The ability of cyanobacteria to survive extreme environmental conditions can be exploited for amelioration of the salt affected soils as they can reduce the salt content and promote levels of C, N, and P including moisture content of the salt affected soils. It has been noticed that cyanobacteria induces soil aggregation and water permeability, and are quite useful in improving quality of poor structured soils of arid or sub-arid areas. Rogers and Burns (1994) investigated that inoculation of cyanobacteria enhanced the stability of soil aggregate (important characteristics of good soil and noticed the resistance of aggregates to wetting and physical disruption); that improved WHC and aeration in soils. Such organisms reduce the compaction and sodicity of soils through improvement in the level of organic carbon, WHC, aeration and support the biodiversity of other microflora.

Cyanobacteria as Bio-fertilizers

Cyanobacteria fix atmospheric papan class="Chemical">n class="Chemical">N2 by forms, i.e., free-livinpan>g and symbiotic associations with partners such as water fern Azolla, cycads, Gunnera, etc. A list of free-living and symbiotic N2 fixing cyanobacteria has been described in Table . Some cyanobacterial members are endowed with the specialized cells known as heterocyst – thick-walled modified cells, which are considered site of nitrogen fixation by n class="Chemical">nitrogenase enzyme. The enzyme is a complex, catalyzes the conversion of the molecular N2 into reduced form like ammonia (Singh et al., 2011). The fixed nitrogen may be released in the form of ammonia, polypeptides, free amino acids, vitamins, and auxin-like substances; either by secretion or by microbial degradation after the cell death (Subramanian and Sundaram, 1986). Nitrogen-fixing ability has not only been shown by heterocystous cyanobacteria but also by several non-heterocystous unicellular and filamentous genera (Table ). Cyanobacteria can contribute to about 20–30 kg N ha-1 as well as the organic matter to the soil, quite significant for the economically weak farmers unable to invest for costly chemical nitrogen fertilizer (Issa et al., 2014). There is a little knowledge on commercial byproducts or biofertilizers but several cyanobacterial species such as Anabaena variabilis, Nostoc muscorum, Aulosira fertissima, and Tolypothrix tenuis found to be effective biofertilizers. Many Asian countries like China, Vietnam, India, etc., have been utilizing cyanobacteria in paddy cultivation as the alternative to nitrogen fertilizers (Venkataraman, 1972; Lumpkin and Plucknett, 1982). It has been reported that N availability to plants is increased due to application of cyanobacteria in agriculture ecosystems, particularly the rice fields (Stewart et al., 1968; Peters et al., 1977; Singh and Singh, 1987). Several researchers have investigated that inoculation of cyanobacteria (in vitro) in wheat crops, could enhance the plant shoot/root length, dry weight, and yield (Spiller and Gunasekaran, 1990; Obreht et al., 1993; Karthikeyan et al., 2007, 2009), but the agronomic efficiency has not been evaluated (Gantar et al., 1991, 1995a,b; Kaushik, 2012).

It has also been suggested that cyapan class="Chemical">nobacteria can improve the bioavailability of phosphorus to the plants by solubilizing anclass="Chemical">pan>d mobilizing the insoluble organic phosphates present in the soil with the help of phosphatase enzymes. Cyanobacteria have the ability to solubilize the insoluble form of (Ca)3(PO4)2, FePO4, n class="Chemical">AlPO4, and hydroxyapatite [Ca5(PO4)3OH] in soils and sediments (Bose et al., 1971; Dorich et al., 1985; Wolf et al., 1985; Cameron and Julian, 1988). There are two hypotheses regarding the mechanism of solubilization of phosphate by cyanobacteria;

Cyanobacteria synthesize a chelator for n class="Chemical">Ca2+ which drives the dissolution to the right without chanclass="Chemical">pan>ging the pH of growth medium (Cameron and Julian, 1988; Roychoudhury and Kaushik, 1989) as menpan>tioned below-

The other assumption is that cyanobacteria release n class="Chemical">organic acids, which can solubilize class="Chemical">pan> class="Chemical">phosphorus through following reaction (Bose et al., 1971) as given below-

Besides the above said two mechanisms, there is also a third possibility. Opan class="Chemical">nce an inorganic phosphate is solubilized, the resulting PO43- is scavenged by the growing population of cyanobacteria for their own nutrition needs, and after their death, of the cell locked PO43- released in the soils, is easily available to plants and other organisms following mineralization (Arora, 1969; Saha and Mandal, 1979; Mandal et al., 1992, 1999).

Fuller and Roger (1952) observed that uptake of papan class="Chemical">n class="Chemical">phosphorus by planclass="Chemical">pan>ts from algal materials was greater than that from the inorganic phosphates, when both were provided in equal amounts over a longer period of time. They also proposed the hypothesis that cyanobacteria could remove available phosphorus from the sphere of chemical fixation in soil by incorporating it into cell constituents or by absorbing it in excess amounts, and then releasing it gradually for plants over a period of time through exudation, autolysis or microbial decomposition of dead cells.

Cyanobacteria as Bio-control Agents

The antagopan class="Chemical">nistic effects of cyanobacteria against different plant diseases have been presented in Table . Cyanobacteria produce a variety of biologically active compounpan>ds of antibacterial, antifungal, antialgal, and antiviral potential (Teuscher et al., 1992; Dahms et al., 2006). These bioactive compounds belong to the group of polyketides, amides, alkaloids, fatty acids, indoles, and lipopeptides (Abarzua et al., 1999; Burja et al., 2001). In addition cyanobacteria produce a broad spectrum of anti-algal compounds which inhibit growth of pathogens by disturbing their metabolic and physiological activities (Dahms et al., 2006).

The cell constituepan class="Chemical">nts of cyanobacteria are known to reduce the incidence of Botrytis cinerea on strawberries and Erysiphe polygoni causing powdery mildew on turnips and damping off disease in tomato seedlings, besides reducing the growth of saprophytes—Chaetomium globosum, Cunninghamella blakesleeana, and Aspergillus oryzae, and plant pathogens such as Rhizoctonia solani and Sclerotinia sclerotiorum (Kulik, 1995). Several researchers reported that compounds like Fischerellin from Fischerella muscicola, shows antifungal activity against several plant pathogenic fungi such as Uromyces appendiculatus (brown rust), Erysiphe graminis (powdery mildew), Phytophthora infestans and Pyricularia oryzae (rice blast), but it was less effective against Monilinia fructigena (brown rot) and Pseudocercosporella herpotrichoides (stem break; Hagmann and Juttner, 1996; Papke et al., 1997).

Among cyapan class="Chemical">nobacteria, Nostoc muscorum has been shownpan> to be antifungal against soil fungi and especially those producing “damping off” (De Caire et al., 1990). The fungus Sclerotinia sclerotiorum, causes “white mold,” one of the most polytheist plant pathogens, mostly affecting compositae notably lettuce (Lactuca sativa L.) and other species of rosette plants (Tassara et al., 2008). Extracts from N. muscorum inhibited the in vitro growth of the fungal plant pathogens such as n class="Species">S. sclerotiorum (Cottony rot of vegetables and flowers) and Rhizoctonia solani (root and stem rots; Kulik, 1995). Biondi et al. (2004) reported that Nostoc sp., a known potential cryptophycin producer, is the source of natural pesticides against the fungi, insects, nematodes. Zulpa et al. (2003) ascertained that N. muscorum also inhibited the growth of other fungi producing the “wood blue stain” [bluish or grayish discoloration of sapwood caused by certain dark-color fungi (Aureobasidium, Alternaria, Cladosporium, etc.)] on the surface and in the interior of the wood (Zulpa et al., 2003). It seems that efficient cyanobacterial strains can be used as bio-control agents to secure higher agriculture yield. New assays are using the cyanobacterial metabolites for obtaining commercial products for sustainable agriculture development. However, information about the bio-controls shows most experiments have been conducted under lab conditions, and very few in the natural agriculture fields. Therefore, there is need for an extensive research to find out the feasibility to apply cyanobacteria as the potential bio-control agents against various plant diseases.

Cyanobacteria in Reclamation of Salt Affected Soils

Cyanobacteria could be playipan class="Chemical">ng a potential role in the reclamation of salt affected (generally termed as Usar land in some parts of India), arid or sub-arid sclass="Chemical">pan> class="Chemical">oils. For amelioration of salt affected lands, chemical methods of using gypsum, sulfur or excessive irrigation applied (Dhar and Mukherji, 1936), are not so cost-effective or environment friendly. Basically, salt affected soils (alfisol/sodic/alkaline/saline) are less productive, rigid soils impermeable to water due to the presence of excessive salts in the upper layers. They can be classified as alkaline and/or saline depending on the salt content. The alkaline soil is characterized by a high pH, high exchangeable Na, measurable amounts of carbonates, and it undergoes extensive clay dispersion (deflocculation due to the high zeta potential of active Na+). The poor hydraulic conductivity and reduced soil aeration make the soils infertile. The saline soil is characterized by high amount of soluble salts (electrical conductivity more than 4 dS cm-1), imparting high osmotic tension to plant roots for absorption of water and nutrients (Pandey et al., 1992). For the first time, Singh (1961) suggested that cyanobacteria could be used as tool for reclamation of Usar soils as they form a thick stratum on the soil surface and conserve the organic C, N, and P as well as moisture, and convert the Na+ clay to Ca2+ clay. Organic matter and N added by the cyanobacteria in such soils helps binding of the soil particles and thus, improves soil permeability and aeration (Singh, 1961). Since the cyanobacteria are capable of solubilizing nutrients from insoluble carbonate nodules through the secretion of oxalic acid (Fritsch, 1945; Singh, 1961); they improve the physico-chemical quality of saline and alkali soils such as soil aggregation by lowering the pH, electrical conductivity, and hydraulic conductivity (Kaushik and Subhashini, 1985). There are certain physiological advantages associated with cyanobacteria which enable them withstand these stresses:

Curtailment of n class="Chemical">Na+ influx (Apte et al., 1987)

Accumulation of inorganic (K+ ion) or organic osmoregulators (n class="Chemical">sugars, n class="Chemical">quaternary amines, etc.; Reed et al., 1984)

Cyanobacterial applicatiopan class="Chemical">n to organically poor semi-arid soils can play a significanclass="Chemical">pan>t role in their reclamation. The soils in these deserts or semi-arid regions are characterized high compaction, low fertility, and water deficiency; and also associated with problems of salinity and sodicity (Nisha et al., 2007); result in poor aeration and n class="Chemical">water infiltration, more soil erosion, and poor diversity of micro-flora. The poor physico-chemical characteristic of soils ultimately has an adverse impact on the plant growth and productivity. Cyanobacteria develop a superficial network of the trichomes/filaments on the soil, which not only binds the soil particles, but also result in enmeshing of the soil particles at depth (Nisha et al., 2007). Cyanobacteria, as carbon and nitrogen fixers, can contribute to the improvement of soil nutrient status of organic carbon and nitrogen in arid soils. Cyanobacterial species such as Anabaena oscillarioides, A. aphanizomenoides, and Microcystis aeruginosa exhibited the salt tolerance ability ranging from 7 to 15 g/L (Coutinho and Seeliger, 1984; Moisander et al., 2002).

They are also knowpan class="Chemical">n for the production of EPS, which help soil particles to bind together (Mazor et al., 1996), and thus play a major role in improvement of soil moisture owing to their hygroscopic nature. Flaibani et al. (1989) reported that exopolysaccharides from cyanobacteria also contribute to reclamation of the desert soils.

Cyanobacteria in Bioremediation

Cyanobacteria as bioremediators, have some advapan class="Chemical">ntages over other microorganisms because of their photoautotrophic nature and ability to fix atmospheric N2 which makes them self-sufficient for growth and maintenanclass="Chemical">pan>ce and adaptability to survive in polluted and heavily polluted environments (Sokhoh et al., 1992). Cyanobacteria show a great potential for the treatment of various types of environmental contaminates such as pesticides (Megharaj et al., 1994), crude oil (Sokhoh et al., 1992; Al-Hasan et al., 1998, 2001), naphthalene (Cerniglia et al., 1980a,b), phenanthrene (Narro et al., 1992), phenol and catechol (Shashirekha et al., 1997), heavy metals (Singh et al., 2011b), and xenobiotics (Megharaj et al., 1987) either through their accumulation or degradation. Due to high metal sorption capacity and high multiplication rate, cyanobacteria could play a potential role in the detoxification of various industrial effluents such as from oil refinery, brewery and distilleries, paper mill, sugar mill, dye and pharmaceuticals industries. Cyanobacteria may be used for tertiary treatment of urban, agro-industrial effluents (Vílchez et al., 1997), and in turn, can help mitigate eutrophication and metal toxicity problems in aquatic ecosystems. Because of their photosynthetic nature, some cyanobacterial species are conferred with the additional advantages like higher interior pH, which is almost two units higher than the surrounding pH conditions and this confers resistance to mass transfer of pollutants out of their biofilms from the external environment and thus helps in removal of heavy metals from the wastewaters (Liehr et al., 1994; Vijayakumar, 2012). Currently, cyanobacteria have been used efficiently as low-cost bioremediating agents for treatment of N-, P-rich dairy wastewaters and converting these nutrients into biomass (Lincoln et al., 1996; Singh et al., 2011a). Cyanobacteria accumulate very high concentration of pesticides (Vijayakumar, 2012). Cyanobacterial members such as n class="Species">Synechococcus elongatus, Anacystis nidulans, and Microcystis aeruginosa degrade many organo-phosphorus and organo-chlorine insecticides from the polluted aquatic systems (Vijayakumar, 2012). El-Bestawy et al. (2007) reported that several cyanobacterial genera Oscillatoria, Synechococcus, Nodularia, Nostoc, Microcystis, and Anabaena have the ability to remove or degrade the lindane residues. According to Forlani et al. (2008), cyanobacteria like Anabaena sp., Lyngbya sp., Microcystis sp., and Nostoc sp. degrade the broad range organo-phosphorous herbicide glyphosate, and the mineralized glyphosate, is consumed as the phosphorus source. Lipok et al. (2007, 2009) demonstrated that Spirulina sp. could degrade the glyphosate herbicide. It is also reported that Synechocystis sp. successfully mineralized the aniliofos herbicide, and used the product as phosphate source. Thus it is evident that the cultivation of cyanobacteria in wastewater lagoons may have great potential to degrade the pollutants and pesticides, and help in reducing the pollution load and support growth of other microbial populations for reductions in the BOD and COD.

Several investigatiopan class="Chemical">ns showed that cyanobacteria degrade crude oil and other complex organic compounpan>ds such as surfactants (Radwan and Al-Hasan, 2000; Raghukumar et al., 2001; Mansy and El-Bestway, 2002). For example, cyanobacterial species Oscillatoria salina, Plectonema terebrans, Aphanocapsa sp., and Synechococcus sp., develop mats in aquatic environments, and have been successfully used in the bioremediation of oil spills in different parts of the world (Raghukumar et al., 2001; Cohen, 2002). Not only oil-contaminated waters but also oil-contaminated soils be successfully remediated using a naturally occurring cyanobacterial–bacterial associations (Sorkhoh et al., 1995). Al-Hasan et al. (1998) reported that n class="Species">Microcoleus chthonoplastes and Phormidium corium isolated from oil-rich sediments of the Arabian Gulf, were able to degrade n-alkanes. It is also reported that Oscillatoria sp. and Agmenellum sp. oxidize naphthalene to 1-naphthol (Cerniglia et al., 1979, 1980a); Oscillatoria sp. oxidize biphenyl to 4-hydroxybiphenyl (Cerniglia et al., 1980b) and Agmenellum sp. metabolizes phenanthrene into trans-9,10-dihydroxy-9,10-dihydrophenanthrene, and 1-methoxy-phenenthrene (Narro, 1985). The role of cyanobacterial species in removal of heavy metals in different ecosystems is given in the Table . The biodegradation potential of cyanobacteria can be enhanced through genetic engineering (Kuritz and Wolk, 1995), and be used as the economical and maintenance-free remediation technology for contaminated eco-systems. However, ecological and environmental concerns and regulatory constraints are the major obstacles for releasing the transgenic cyanobacteria for bioremediation purposes under field conditions. Since most of the research on bioremediation by engineered cyanobacteria is of basic nature, there is growing need for the regulatory, security or economical-beneficial systems, which may decipher their bioremediation potential tool into reality.

Cyanobacteria as Plant Growth Promoters

Cyanobacteria release extracellular plapan class="Chemical">nt growth promoting substances; some described as hormones (Table ) like gibberellins (Singh and Trehanclass="Chemical">pan>, 1973), cytokinin (Rodgers et al., 1979), auxin (Ahmad and Winter, 1968), or abscisic acids (Marsalek et al., 1992). Others are explained as vitamins, particularly vitamin B (Grieco and Desrochers, 1978) or amino acids (Vorontsova et al., 1988), antibiotics and toxins. The production of phytohormones by some potential cyanobacteria is outlined in Table .

Most of the studies on the plapan class="Chemical">nt growth promoting effects of cyanobacteria related to paddy crop revealed that cyanobacterial inoculation could enhance rice seed germination, root and shoot growth (Misra and Kaushik, 1989a,b). It is also evident that co-inoculation of cyanobacteria with class="Chemical">pan> class="Species">wheat enhanced root dry weight and chlorophyll (Obreht et al., 1993). Gantar et al. (1995a,b) observed that extracellular substances released by cyanobacteria that colonize wheat plant roots showed significant effect on plant growth, though the agronomic efficiency was not evaluated. Due to their natural diversity, the capacity of cyanobacteria to grow in a variety of locations, even those unfit for agriculture, could be exploited. The fast cyanobacterial cell growth and simple nutritional requirements mainly water, sunlight, and CO2 (Ruffing, 2011) provides a wide scope for the commercial application of cyanobacterial species as plant growth promoters.

Cyanobacteria as Source of Bio-energy

Cyanobacteria are the upan class="Chemical">nique group of photosynthetic bio-agents that can grow at a fast rate due to their simple cell structure and minimum requirement of nutrients accompanied by the capacity to produce bio-energy including bio-diesel, bio- or syngas, bio-hydrogen, etc. (Kumar and Singh, 2016) (Figure ). Carbon dioxide (CO2) is taken up by cyanobacteria through photosynthesis, to be converted to carbon-rich lipids (Table ) that can be used in production of bio-fuels. Cyanobacteria also produce molecular hydrogen (H2) which could be the better option and the ideal substitute of for fossil fuels. These microbes can produce different feed-stock for energy generation like H2 (by photosynthesis), lipids for biodiesel, jet fuel and hydrocarbons, isoprenoids for gasoline and carbohydrates for ethanol production (Parmar et al., 2011; Rosgaard et al., 2012). The cyanobacterial biomass containing lignocellulosic compounds can also be processed for syngas production followed or not by a Fischer–Tropsch process and gasification/liquefaction for H2 production (Lawson et al., 2011). The advantage of using molecular H2 as the clean fuel is one of the most abundant elements in the universe, and has maximum energy per unit weight (122 KJ g-1). On a weight basis, it is calculated that the heating value of H2 is 141.65 MJ Kg-1, which is the highest amongst known fuels (Ali and Basit, 1993). It can be stored as gas-metal hydride or as liquid, and has greater energy conversion efficiency than petroleum. H2, if used as a fuel, will not cause environmental pollution because its only by-product is water. Several cyanobacterial genera including Anabaena, Calothrix, Oscillatoria, Cyanothece, Nostoc, Synechococcus, Microcystis, Gloeobacter, Aphanocapsa, Chroococcidiopsis, and Microcoleus are known for their ability to produce H2 under various culture conditions (Masukawa et al., 2001; Parmar et al., 2011; Nozzi et al., 2013) (Figures and ). Cyanobacteria produce H2 by two ways (Pinzon-Gamez et al., 2005):

Productiopan class="Chemical">n of H.

Heterocystous and non-diazotrophic H.

Mediated by the n class="Chemical">nitrogenase enzyme which catalyzes the followinpan>g reaction

Reversible activity of n class="Chemical">hydrogenase enzymes

Although cyanobacterial papan class="Chemical">n class="Chemical">H2 productionpan> is a clean and green technology, the limitation in this process is lesser H2 production that makes unsuitable for being economically feasible (Tiwari and Pandey, 2012). There are certain shortcomings associated with these processes which form an obstacle in the scale up of H2 production from cyanobacteria. The hydrogenase enzyme responsible for H2 production is extremely sensitive to O2, and therefore, the concurrent production of O2 poses a serious limitation. The process through which H2 is produced by cyanobacteria, has its merits and de-merits both in terms of technology and productivity. Undoubtedly, based on the research reports, it may be deduced that this field is yet preliminary and without any potential practical application. These processes are yet to be evaluated and modified for productivity and cost the of n class="Chemical">H2 commercialization.

Besides production of bio-fuel apan class="Chemical">nd molecular H2, the cyanobacterial biomass canclass="Chemical">pan> be used to produce biogas via anaerobic digestion or fermentation (Table ). The organic biopolymers (carbohydrates, lipids, and proteins), in the cyanobacterial biomass are hydrolyzed and broken down into monomers, which are then subjected to anaerobic digestion to produce biogas (mixture of CH4 and CO2). During biogas production, CO2 is the second main component (approximately 25–50%), which can be removed to obtain bio-methane. The calorific value of biogas can be significantly enhanced by removing the CO2 during n class="Chemical">bio-methane production (Hankamer et al., 2007). CH4 or bio-methane can be used as the compressed natural gas in vehicles, which is going to be more environmentally friendly than the fossil fuels like gasoline/petrol and diesel. Converti et al. (2009) reported biogas production and purification using a two-step bench-scale biological system, consisting of fed-batch pulse-feeding anaerobic digestion of mixed sludge, followed by CH4 enrichment of biogas by the use of the cyanobacteria like Arthrospira platensis. The ratio of CH4 and CO2 ranges between 70.5–76.0% and 13.2–19.5%, respectively. The data on CO2 removal from biogas revealed the existence of a linear relationship between the rates of A. platensis growth and CO2 removal from biogas, and this allows the estimation of carbon utilization efficiency of cyanobacterial biomass to the extent of almost 95% (Converti et al., 2009).

The C/n class="Chemical">Npan> ratio is one of the important factors influencing CH4 production during the anaerobic digestion (Zhong et al., 2012). The high protein content of the cyanobacterial biomass (low C/N ratio) compared to terrestrial plants leads to a high ammonia release during anaerobic digestion, thus inhibiting the anaerobic micro-flora responsible for CH4 production (Sialve et al., 2009). Anaerobic digestion of the protein rich cyanobacterium n class="Species">Spirulina maxima, containing up to 60–71% of proteins, releases an extremely high concentration of ammonia (up to 7000 mgL-1). The methanogens are perhaps among the most sensitive micro-flora to high NH3. It is worth noting that methanogenic bacteria can, however, acclimate to high concentrations of ammonium Sialve et al. (2009). It is suggested that a significant increase in CH4 production can be achieved by adding carbon-rich corn straw to the co-digestion process with cyanobacterial biomass (Sialve et al., 2009). According to their result output the C/N ratio of 20/1 was found to be the best in terms of CH4 productivity, which increased by 61.69% during the study as compared to control. Therefore, it may be recommended that co-digestion of cyanobacterial biomass containing high protein contents (low C/N ratio) with plant residues (low protein contents or high C/N ratio) could be one of the options for efficient CH4 production and waste treatment.

The cultivation of these greepan class="Chemical">n bio-agents (cyanobacteria farming) can efficiently be done at different scales, lesser space, time and under diverse conditions (fresh as well as waste and unused waters) to achieve high value bio-fuel products. The filamentous cyanobacteria could be beneficial since contaminated and wastewaters may be used for large scale biomass production and at the same time, treating wastewater to remove pollutants. The cyanobacterial biomass quality and quantity can be manipulated with the help of several physico-chemical treatments to achieve the desired cyanobacterial biomass having good quality bio-fuel products. Bio-fuel production using cyanobacteria farming offers various advantages over other bio-agents may be:

Fast growth and multiplication capability of cyanobacteria can meet huge demand for bio-fuels using limited resources.

Cyanobacterial cultivation consumes less fresh n class="Chemical">water than the croplands, anclass="Chemical">pan>d wasten class="Chemical">waters can equally be utilized for the generation of biomass.

Under elevated n class="Chemical">CO2 concentrations, cyanobacterial biomass can be produced at higher efficienpan>cy.

Green house gases (n class="Chemical">nitrous oxide, CH4, etc.) emissions from crop fields can be minpan>imized through cultivation of cyanobacteria for bio-enpan>ergy production, and

Cyanobacteria farming for generation of bio-fuels may be potentially more cost-effective, eco-friendly, and sustainable than the conventional agriculture farming.

It seems that genetically epan class="Chemical">ngineered cyanobacteria can be potentially used for the production of a number of bio-fuels [acetone, butanol, ethanol, alka(e)nes, etc.] in the economically sustainable way (Figure and Table ). However, different biotechnological, environmental and economic challenges have to be overcome before energy products from recombinant cyanobacteria (Apt and Behrens, 1999). Further, both the production technology and downstream processing of the end products can effectively be improved to obtain super quality bio-fuels from cyanobacteria.

Cyanobacteria in CO2 Sequestration and Climate Change Mitigation

n class="Chemical">Carbon dioxidepan> is one of the purported GHGs, primarily responsible for global warming and needs to be mitigated. The strategies to reduce CO2 emissions include energy savings, development of renewable bio-fuels, and CCS. CCS, a viable tool needs to be explored to enhance the efficiency of such a strategy (Rau et al., 2007), and several approaches being considered are (a) capture of point-source CO2 from power plants or other industrial sources and subsequent injection of the concentrated CO2 underground or into the ocean (Benson and Orr, 2008); (b) expansion of biological carbon sequestration of atmospheric CO2 by measures such as reforestation, changes in land use practices, increased carbon allocation to underground biomass, production of biochar and enhanced bio-mineralization (Jansson et al., 2010).

The n class="Chemical">CO2pan> sequestration by cyanobacteria is receiving increased awareness in alleviating the influence of rising CO2 concentrations in the atmosphere (Kumar et al., 2011). Being photosynthetic, cyanobacteria contribute to a large share of the total photosynthetic conversion of solar energy and assimilation of CO2. The CO2 fixation rate in cyanobacteria is about 10–50 times faster than the terrestrial plants. Thus the use of these biological agents is considered one of the effective approaches to reduce the concentration of atmospheric n class="Chemical">CO2 and thereby, to help in mitigation of possible global warming (Chisti, 2007). The captured CO2 in the cyanobacterial biomass can be stored in the form of organic molecules, which can then be used in various ways. In paddy field soils, the cyanobacteria contribute significantly to both organic and nitrogenous contents (Singh, 2014).

It is anticipated that half of global photosypan class="Chemical">nthesis is contributed by phytoplankton, which mostly includes cyanobacterial members (Fuhrman, 2003). Among these, about 25% of the total global photosynthesis can be accounted for by only two efficient marine cyanobacterial genera, Synechococcus and Prochlorococcus (Rohwer and Thurber, 2009). Many cyanobacteria are halophilic and, therefore, they can be cultured in marine waters, saline drainage water, or brines from petroleum refining industry or CO2 injection sites, thereby sparing freshwater supplies (Jansson and Northen, 2010). Combustion of fossil fuels such as coal, oil, gas, etc. is the major source of flue gas (mixture of N2, CO2, O2, and water vapors) emission globally. Since the flue gas released from the power plants contains high concentrations of CO2 and has high temperatures (about 120°C), the cyanobacterial bio-fixation of CO2 may warrants the use of thermophilic cyanobacterial species that are tolerant to both high CO2 and temperature (Badger and Price, 2003; Ono and Cuello, 2007). Biomass production and CO2 uptake in cyanobacteria exposed to higher CO2 levels from flue gas or other streams have been followed for a variety of cyanobacterial species such as Aphanothece microscopica (Jacob-Lopes et al., 2008). Several thermophilic cyanobacterial members (Synechococcus aquatilis, Chlorogloeopsis sp. etc.) having the capability to tolerate higher temperatures, can be used for CO2 sequestration from the flue gas. Though the major problem associated with the cyanobacterial or biological use of CO2 is the high temperatures of flue gas and the presence of NOx, SOx as well as other impurities of the fossil fuel used (Kumar et al., 2011). However, the employment of thermophilic and elevated CO2 tolerant cyanobacterial species in large water reservoir experiments can solve the problem of NOx, SOx, etc. on CO2 sequestration from flues gas as suggested by Jansson and Northen (2010). Thermophilic cyanobacteria such as Synechococcus lividus and Mastigocladus laminosus inhabiting range from 63–64°C and 73–74°C, respectively (Miller et al., 2007). In the over all, the large body operations regarding CO2 sequestration from flue gas owing to the application of thermophilic cyanobacteria may be economically feasible as:

Thermophilic cyanobacteria can efficiently assimilate significant quantity of n class="Chemical">CO2 from n class="Chemical">flue gas;

Thermotolerant cyanobacterial strains may be unaffected by the n class="Chemical">NOx and SOx inpan> n class="Chemical">flue gas;

Use of thermophilic cyanobacteria may minimize the cost of cooling the n class="Chemical">flue gas;

Municipal wasten class="Chemical">water mediated nutrient supply can reduce the operation cost; and

Freshn class="Chemical">water and marinpan>e cyanobacterial species can be used for a broad range survival.

There are additional factors like the availability of light, pH, papan class="Chemical">n class="Chemical">O2 removal, suitable designpan> of the experimental systems, culture density, and the proper agitation of the systems that will affect significantly CO2 sequestration. Cyanobacterial CO2 fixation in photobioreactors has recently gained renewed interest in being the promising strategy for CO2 mitigation. A number of studies have been conducted during the past few decades (Hanagata et al., 1992; Maeda et al., 1995; Hirata et al., 1996a,b; Rangel-Yagui et al., 2004) related to this strategy for n class="Chemical">CO2 sequestration. The use of photobioreactors provides principal advantages over open-pond system, i.e., controlled environmental conditions and optimized space/volume utilization, leads to increase in cyanobacterial productivity; efficient use of land (Muhs, 2000; Ono and Cuello, 2004); higher water-use efficiency since water loss due to evaporation could be easily prevented, and improved harvesting efficiency. Also, genetically engineered cyanobacterial strains, if appropriate, could be used without disturbing the natural environment.

Through photosynthesis apan class="Chemical">nd calcification, cyanobacteria have the potenpan>tial to capture n class="Chemical">CO2 from n class="Chemical">flue gas and store it precipitated as CaCO3/CaHCO3 (Mazzone et al., 2002; Lee et al., 2004). Calcium is abundant in many terrestrial, marine and lacustrine ecosystems. By using halophilic cyanobacteria, seawater or brines, for example agricultural drainage water, or saline water produced from petroleum production or geological CO2 injections, can serve as the potential calcium sources for the calcification process. Calcification can further be boosted by supplying calcium from gypsum (Mazzone et al., 2002) or silicate minerals, possibly in connection with biologically accelerated weathering. However, identification and characterization of cyanobacterial species that would show significant CO2 assimilation rates at elevated temperature and CO2 concentrations is still required. We have to investigate calcification at higher CO2 concentrations, such as in flue gas, and identify how photosynthetic machinery and light harvesting systems can be automated in cyanobacteria cultivated in open pond environment or in photobioreactors. A better understanding of the biochemical and genetic mechanisms that carry out and regulate cyanobacteria-mediated CO2 sequestration should put us in a position to further optimize these steps by application of advanced technique of genetic engineering.

Cyanobacteria in Reduction of Methane Emissions

n class="Chemical">Methanepan> (CH4) has negative consequences as it is a potent GHG with approximately 20 times the impact of CO2 (Singh, 2011). Anthropogenic activity accounts for the majority of global CH4 increase, with natural emissions accounting for the rest. Anthropogenic mediated CH4 emissions are due fossil fuel use, livestock farming, land filling and biomass burning. Natural sources of CH4 are estuaries, rivers, lakes, permafrost, gas hydrates, wetlands, oceans, wildfires, vegetation, termites, and wild animals. Flooded paddy fields are also one of the major contributors to atmospheric CH4 increase due to methanogenesis in anaerobic flooded paddy soils. It is assumed that with the increased n class="Species">human population and food requirements, greater waste generation, and greater use of fossil fuels, its concentration in the atmosphere will in all likelihood increase further. Therefore, a suitable eco-friendly and viable tool will require mitigating the problem of CH4. Cyanobacteria could be a big prospect to overcome the global warming problem caused by the GHGs generated from anthropogenic activities (Cuellar-Bermudez et al., 2014). Cyanobacteria may possibly minimize the emissions of CH4 from flooded rice soils at the levels of production, transport, and consumption. Bio-agents like methanotrophs (Tiwari et al., 2015) can play a very significant role to remove significant amount of the most potent and dangerous GHGs such as CH4 from the soils of various ecosystems (Singh, 2013a; Singh and Pandey, 2013; Singh and Singh, 2013a) in association with cyanobacteria. Information on interaction between cyanobacteria and methanotrophs with reference to methane flux regulation in paddy fields is completely lacking to date (Kaushik and Venkataraman, 1982). It is assumed that cyanobacteria may enhance the oxygen concentration in rhizosphere of paddy and consequently may enhance the methane uptake activity of methanotrophs. In addition, these biological agents can minimize the global warming potential from flooded paddy apart from their ability to fix the atmospheric N2 in the paddy soils. The O2, released during photosynthesis by cyanobacteria into the flooded soils, can liberate into the soil and create an aerobic environment, not friendly for CH4 genesis (Prasanna et al., 2002). At the same time, the O2 released by cyanobacteria, can augment CH4 oxidation by enhancing the population and activity of aerobic methane-oxidizing bacteria (methanotrophs) in flooded paddy soils. The combined application of organic amendment such as FYM and cyanobacteria can not only give the higher paddy yield, but may also contribute to production of lesser CH4 during paddy cultivation than the application of FYM alone (Singh et al., 2010; Singh and Pandey, 2013). Application of cyanobacteria reduces methane flux without affecting rice yields, and can be used as the practical mitigation option for minimizing the global warming potential of flooded paddy ecosystems and enhancement by N2 fixation (Prasanna et al., 2002). It appears that increasing the diversity of microbes (Singh, 2015a) including cyanobacteria and methanotrophs in paddy fields can be an innovative strategy to enhance crop productivity and reduce the CH4 emissions from the agriculture fields in the long-term (Singh and Singh, 2012; Singh, 2014). It is suggested that the application of cyanobacteria and their contributions as the N fertilizer replacement would be cost-effective, eco-friendly, and the safer means for degraded land restoration (Pandey et al., 2014; Singh, 2014, 2015b), and also to conserve the methanotrophic diversity and CH4 consumption in the long-term (Figure ).

Benefits of cyapan class="Chemical">nobacterial bio-fertilizers for sustainable agriculture and mitigating the problems of CH.

Cyanobacteria as Food Supplements

Cyanobacteria as food supplemepan class="Chemical">nts for humans are available in the market inpan> different forms such as tablets, capsules, and liquid (Radmer, 1996). They are considered to enhance the nutritive value of pastas, snack foods, candy bars or gums, and beverages (Liang et al., 2004). They can act as the nutritional supplement or represent a source of natural food colorants (Nelis and DeLeenheer, 1991; Borowitzka, 1999; Muller-Feuga, 2000; Branen et al., 2002; Becker, 2004; Rangel-Yagui et al., 2004; Bhaskar et al., 2005; Soletto et al., 2005). The most commercial cyanobacterial strain (Table ) used for human nutrition is Spirulina (Arthrospira), because of its high protein content and excellent nutritive value (Desmorieux and Decaen, 2005; Soletto et al., 2005). In many countries including Chile, Mexico, Peru, and Philippines; some cyanobacterial members such as Spirulina, Anabaena, and Nostoc are consumed as human food. Arthrospira platensis (Spirulina platensis) is grown on large scale using either raceway ponds or sophisticated photobioreactors and marketed as powder, flakes, tablets or capsules. It contains more than 60% proteins and is rich in beta-carotene, thiamine, and riboflavin, and is considered to be one of the richest sources of vitamin B12 (Plavsic et al., 2004; Prasanna et al., 2010). It is used as a food supplement because of its richness in nutrients and digestibility (Brown et al., 1997; Bandaranayake, 1998; Sinha et al., 1998). Kulshreshtha et al. (2008) claimed that Spirulina contains a wide spectrum of prophylactic and therapeutic nutrients including B-complex vitamins, minerals, proteins γ-linolenic acid and super antioxidants such as β-carotene, n class="Chemical">Vitamin E, trace elements, and a number of unexplored bioactive compounds (Nakamura et al., 1982; Garcia_Pichel et al., 1993; Bohm et al., 1995; Rimbau et al., 2001; Sinha et al., 2001; Kedar et al., 2002; Rissanen et al., 2002; Romay et al., 2003; Benedetti et al., 2004; Rajeev and Xu, 2004; Subhashini et al., 2004).

Conclusion and Future Recommendations

It is imperative for the healthy agro-ecosystem to gain sustainability in the true sense in order that it conserves the nature and natural resources, and also maintains the complexity and diversity of the ecosystems. It supports and sustains sufficient food production for the increasing world population, ensures economic viability, and safer living for both humans as well as other livestock. Above all, it addresses the present day environmental concerns. For poor farmers (especially in developing countries), it is not quite easy to afford the costly chemical fertilizers and pesticides and also feel concerned for the environmental issues. Cyanobacteria in this context can be very effective for enriching sclass="Chemical">pan> class="Chemical">oil organic carbon and nitrogen and enhancing phosphorus bioavailability to the plants. Cyanobacteria are excellent accumulators or degraders of various environmental contaminants such as heavy metals, pesticides, and oil containing compounds. Such ubiquitous bio-agents can also be used for capturing and storage of CO2 that may also lead to climate change mitigations through photosynthesis and biological calcification. They are also the ideal source of variety of bioactive compounds with marked antagonistic properties.

There is enormous scope for the developmepan class="Chemical">nt of bio-agents including cyanobacteria for sustainable agriculture which also takes care of the improvement in the nutrient status of soil and biological control of pest and diseases that may ultimately lead to reductions in the agricultural costs (Singh, 2013b; Singh and Singh, 2013b). However, it is necessary to carry out further inpan>vestigations for exploitation of cyanobacteria with the futuristic goal to achieve the target of sustainable agriculture and environment. In view of the declining soil health and productivity due to increased human activities, the maintenance of environmental sustainability is the challenging task ahead. The cyanobacteria are multi-functional bio-agents for safe and eco-friendly agriculture and environmental sustainability, along with several other uses. To improve their utility in agriculture and associated sectors needs serious attention. Thus there is an urgent need to address certain key issues of exploiting cyanobacteria, the better way. Further, the application of molecular biology has improved our understanding of the effectiveness for betterment of healthy and sustainable agro-ecosystems. Since the use of cyanobacteria to produce valuable chemicals including food supplements is still little explored, there seems a long way to go. In addition to product developments, future research must address the strain improvement of useful cyanobacteria to achieve high quality food and fuel products, maintain high growth rates and survival under harsh environmental conditions. These will be the key factors to leap from laboratory studies to large-scale and profitable bio-fuel production for sustainable agriculture, ecosystem and environmental development.

The utility of cyanobacteria ipan class="Chemical">n sustainable agriculture and environment can be enhanced by genetic manipulations (Golden et al., 1987; Koksharova and Wolk, 2002; Huang et al., 2010; Heidorn et al., 2011). However, the application of genetic engineering to improve bio-fuel production in cyanobacteria is still in its infancy. In future, genetic and metabolic engineering of cyanobacteria are likely to play important roles in improving the economics of cyanobacteria-mediated bio-fuel production. Cyanobacteria can be genetically modified to potentially increase their growth and photosynthetic efficiency, biomass yield, lipid and carbohydrate productivity, improve temperature tolerance, and reduce photo-inhibition and photo-oxidation (Volkmann and Gorbushina, 2006; Volkmann et al., 2006). However, from lab to field condition shift will not be as easy as it has to addressed several issues such as social relevance, political lobbying and fulfillments with the regulatory norms. Besides these, problems related to cross-contamination through use of closed-photo-bioreactors as a substitute of open ponds, it is recommended to be thoroughly examined prior to execution.

Author Contributions

JSS contributed about the role of cyapan class="Chemical">nobacteria in mitigation of GHGs and overall sustainable development. AK described the role of cyanobacteria in biogas and bio-fuel production. ANR suggested about contribution of cyanobacteria in agriculture production and degraded land restoration. DPS contributed about soil nitrogen fixation and an enrichment mediated by cyanobacteria.

Conflict of Interest Statement

The authors declare that the research was conducted ipan class="Chemical">n the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Table 1

Important nitrogen fixing cyanobacterial genera.

Form of Cyanobacteria	Cyanobacterial members
Unicellular	Aphanothece, Chroococcidiopsis, Dermocapsa, Synechococcus, Gloeocapsa (Gloeothece)∗, Myxosarcina, Pleurocapsa∗, Xenococcus
Filamentous heterocystous	Anabaena∗, Anabaenopsis, Aulosira, Calothrix∗, Camptylonema, Chlorogloea, Chlorogloeopsis, Cylindrospermum, Fischerella∗, Gloeotrichia, Hapalosiphon, Mastigocladus, Nodularia, Nostoc∗, Nostochopsis, Rivularia, Scytonema∗, Scytonematopsis, Stigonema, Tolypothrix, Westiella, Westiellopsis
Filamentous non-heterocystous	Lyngbya, Microcoleus chthonoplastes, Myxosarcina, Oscillatoria, Plectonema boryanum, Pseudanabaena, Schizothrix, Trichodesmium

Table 2

Cyanobacterial species exhibiting antagonistic effects against different plant pathogens.

Cyanobacteria	Plant diseases and pathogens	Reference
Calothrix elenkenii	Damping off (Rhizoctonia solani)	Manjunath et al., 2009
Fischerella muscicola	Brown rust (Uromyces appendiculatus), powdery mildew (Erysiphe graminis), rice blast (Pyricularia oryzae)	Hagmann and Juttner, 1996
Nostoc muscorum	Cottony rot of vegetables and flowers (Sclerotinia sclerotiorum) and damping off (Rhizoctonia solani)	De Caire et al., 1990; Kulik, 1995; Tassara et al., 2008

Table 3

Heavy metal removal by some cyanobacterial species.

Heavy metals	Source	Cyanobacteria	Reference
Cd	Sewage water aqueous solution	Nostoc linckia, N. rivularis, Tolypothrix tenuis	Inthorn et al., 1996; El-Enany and Issa, 2000
Co	Sewage and industrial wastewater	N. muscorum, Anabaena subcylindrica	El-Sheekh et al., 2005
Cr	Metal contaminated soil	N. calcicola, Chroococcus sp.	Anjana et al., 2007
Cu	Sewage and industrial wastewater	N. muscorum, A. subcylindrica	El-Sheekh et al., 2005
Hg	Wet biomass	Spirulina platensis, Aphanothece flocculosa	Cain et al., 2008
Mn	Sewage and industrial wastewater	N. muscorum, A. subcylindrica	El-Sheekh et al., 2005
Pb	Sewage and industrial wastewater	N. muscorum, A. subcylindrica, Gloeocapsa sp.	El-Sheekh et al., 2005; Raungsomboon et al., 2006
Zn	Sewage water	N. linckia, N. rivularis	El-Enany and Issa, 2000

Table 4

An overview of production of plant growth promoting chemicals by cyanobacteria.

Type	Cyanobacteria	Reference
Auxins	Anabaena, Anabaenopsis, Calothrix, Chlorogloeopsis, Cylindrospermum, Glactothece, Nostoc, Plactonema, Synechocystis, etc.	Ahmad and Winter, 1968; Mohan and Mukherji, 1978; Selykh and Semenova, 2000; Sergeeva et al., 2002
Gibberellins	Anabaenopsis, Cylindromum, etc.	Singh and Trehan, 1973; Mohan and Mukherji, 1978
Cytokinins	Anabaena, Chlorogloeopsis, Calothrix, etc.	Rodgers et al., 1979; Selykh and Semenova, 2000

Table 5

Some cyanobacterial members and their lipid contents (modified from Sharathchandra and Rajashekhar, 2011).

Cyanobacteria	Lipid contents (%)	Lipid types
Calothrix fusca	22.60	Palmitic acid, linoleic acid
Lyngbya dendrobia	10.55	Palmitic acid, palmitoleic acid, oleic acid, linoleic acid
L. limnetica	26.45	Palmitic acid, oleic acid, linoleic acid
Microcystis aeruginosa	28.15	Tridecanoic acid, palmitic acid, stearic acid, linoleic acid, α-linolenic acid
Nostoc linckia	18.45	Palmitic acid, oleic acid, linoleic acid
Oscillatoria calcuttensis	25.70	Lauric acid, palmitic acid, palmitoleic acid, Heptadecanoic acid, stearic acid, oleic acid, linoleic acid
O. acuminata	24.65	Lauric acid, tridecanoic acid, myristic acid, palmitic acid, palmitoleic acid, heptadecanoic acid, stearic acid, oleic acid, linoleic acid
O. chlorina	16.62	Palmitic acid, stearic acid, oleic acid, linoleic acid, lignoceric acid
O. amoena	18.63	Palmitic acid, oleic acid, linoleic acid, lignoceric acid
O. perornata	14.10	Palmitic acid, palmitoleic acid
Phormidium ambiguum	10.48	Lauric acid, palmitic acid, lignoceric acid
Scytonema bohnerii	22.22	Palmitic acid, linoleic acid

Table 6

Chemical products synthesized by genetically engineered cyanobacteria.

Product	Cyanobacteria members	Reference
1-ButanolFatty acidsIsopreneIsobutyraldehydeIsobutanol	Synechococcus elongatus PCC7942Synechocystis sp. PCC 6803Synechocystis sp. PCC 6803S. elongatus PCC 7942S. elongatus PCC 7942	Lan and Liao, 2011Liu et al., 2011Lindberg et al., 2010Atsumi et al., 2009Atsumi et al., 2009

Table 7

Bio-methane producing cyanobacterial members.

Cyanobacteria	C/N Ratio	Methane yield	Reference
Arthrospira maximaA. platensisMicrocystis sp.Spirulina Leb18Spirulina sp.S. platensis UTEX1926	4.3–5.33–––4.16–	173 mL g-1481 mL g-170.33–153.51 mL0.79 g L-10.35–0.80 m30.40 m3	Inglesby and Fisher, 2012Mussgnug et al., 2010Zeng et al., 2010Costa et al., 2008Samson and Leduy, 1986Converti et al., 2009

Table 8

Some commercial companies involved in production of cyanobacteria as food source (Courtesy of Gantar and Svircev, 2008; Priyadarshani and Rath, 2012).

S. No.	Cyanobacterial genera	Commercial company
1.	Arthrospira (Spirulina)	Siam Algae Co. Ltd, Thailand Earthrise Nutritionals, Irvine, CA, USA Hainan Simai Pharmacy Co., China Klamath Falls Lake, Oregon, USA Lake Chad, Chad Cyanotech Corp., Kailua-Kona, HI, USA Myanmar Spirulina Factory, Myanmar
2.	Aphanizomenon flos-aquae	Blue green fields, USA Vision, USA