| Literature DB >> 23400445 |
Lukasz Lawniczak1, Roman Marecik, Lukasz Chrzanowski.
Abstract
The number of studies dedicated to evaluating the influence of biosurfactants on bioremediation efficiency is constantly growing. Although significant progress regarding the explanation of mechanisms behind biosurfactant-induced effects could be observed, there are still many factors which are not sufficiently elucidated. This corresponds to the fact that although positive influence of biosurfactants is often reported, there are also numerous cases where no or negative effect was observed. This review summarizes the recent finding in the field of biosurfactant-amended bioremediation, focusing mainly on a critical approach towards potential limitations and causes of failure while investigating the effects of biosurfactants on the efficiency of biodegradation and phytoextraction processes. It also provides a summary of successive steps, which should be taken into consideration when designing biosurfactant-related treatment processes.Entities:
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Year: 2013 PMID: 23400445 PMCID: PMC3585901 DOI: 10.1007/s00253-013-4740-1
Source DB: PubMed Journal: Appl Microbiol Biotechnol ISSN: 0175-7598 Impact factor: 4.813
An overview of recent studies on biosurfactant-assisted bioremediation
| Type of biosurfactant | Pollutant | Relevant bioremediator | Established effect | Removal efficiency | Reference |
|---|---|---|---|---|---|
| Rhamnolipids | Phenanthrene |
| Positive—solublization | 99 % after 10 days compared to 84 % without biosurfactant (IC—10 g/l) | Pei et al. ( |
| Rhamnolipids | Anthracene |
| Positive—solubilization | 52 % after 18 days compared to 32 % without biosurfactant for | Cui et al. ( |
| Rhamnolipids (Mono-rhamnolipid) | Hexadecane |
| Positive/negative | 93 % after 4 days compared to 78 % without biosurfactants (IC—500 mg/l) | Zeng et al. ( |
| Rhamnolipids, emulsan and indigenous biosurfactants | Pyrene |
| Positive/negative | 98 % after 10 days compared to 91 % without emulsan (IC—50 mg/l) | Husain ( |
| Rhamnolipids | Polycyclic aromatic hydrocarbons | Alfalfa + arbuscular mycorrhizal fungi + microbial consortium of PAH degraders | Positive—solubilization | 61 % after 90 days compared to 17 % with only phytoremediation (IC—12.85 g/kg of soil) | Zhang et al. ( |
| Rhamnolipids (Mono-rhamnolipid) | Phenol |
| Positive—enhanced cell growth | 99 % after 30 h compared to 87 % without biosurfactant (IC—500 mg/l) | Liu et al. ( |
| Rhamnolipids | Crude oil hydrocarbons | Autochthonous marine microflora | Positive/no effect | Up to 25 % for alkanes after 5 days with biosurfactant alone and 59 % when used with nutrients (IC—823 mg/l) | McKew et al. ( |
| Rhamnolipids | Crude oil hydrocarbons | Autochthonous marine microflora | Positive—increased bioavailability | 96 % for C19–C34 alkane fraction after 18 days compared to 10 % without amendment (IC—5 g/l) | Nikolopoulou and Kalogerakis ( |
| Rhamnolipids | Phenanthrene |
| Negative | 23 % after 8 days compared to 74 % without biosurfactant | Shin et al. ( |
| Rhamnolipids | Phenanthrene |
| Positive/no effect/negative | 91 % after 10 days compared to 68 % without biosurfactant (IC—approx. 500 mg/kg of soil) | Gottfried et al. ( |
| Rhamnolipids | Phenanthrene |
| Positive—mobilization | 47 % after 70 days compared to 36 % without biosurfactant (IC—approx. 200 mg/kg of soil) | Shin et al. ( |
| Rhamnolipids | Diesel oil and biodiesel blends | Microbial consortium | Positive/no effect | 77 % after 7 days compared to 58 % without biosurfactants for blends (IC—approx. 15 g/l) | Owsianiak et al. ( |
| Rhamnolipids | Phenanthrene and pyrene | Ryegrass | Positive—increased uptake | Uptake of phenanthrene and pyrene into ryegrass roots was at 435 and 380 mg/kg, respectively, compared to 77 and 158 mg/kg without biosurfactant | Zhu and Zhang ( |
| Rhamnolipids | Cadmium |
| Positive/negative | Rhamnolipids were toxic at higher concentrations (>45 mg/l), however at 40 mg/l their presence inhibited the toxicity of cadmium ions by reducing their bioavailability | Bondarenko et al. ( |
| Rhamnolipids and organic acids | Copper | Indian mustard and ryegrass | Positive—mobilization | Application of rhamnolipids and other amendments notably increased copper uptake by both plants | Johnson et al. ( |
| Sophorolipid | Hydrocarbon mixture | Autochthonous soil microflora | Positive—solubilization and mobilization | Respectively: 95 % after 2 days, 97 % after 6 days and 85 % after 6 days (IC- 6 mg/g of soil) | Kang et al. |
| Not specified | p,p'-DDE |
| Positive/negative | Biosurfactant amendment enhanced p,p′-DDE accumulation, however a 60 % biomass reduction was observed for | White et al. ( |
| Not specified | Petrochemical oily sludge | Mixed bacterial cultures | Positive—potential solubilization | 91 % of the aliphatic fraction and 52 % of the aromatic fraction after 40 days | Cerqueira et al. ( |
| Not specified | Diesel oil hydrocarbons | Autochthonous soil microflora | Positive/no effect | 77 % of aliphatic hydrocarbons after 15 days compared to 9 % without biosurfactant (IC—450 mg/l) | Martins et al. ( |
| Not specified | Pyrene |
| Positive—solubilization | 48 % for | Das and Mukherjee ( |
IC initial concentration at the start of the experiment
Successive steps which should be taken into consideration during the design of biosurfactant-mediated bioremediation processes
| Design step | Relevant step | Criteria |
|---|---|---|
| I. Initial characterization of the polluted area | 1. Initial recognition of pollutants | Establishment of either single or multi-contaminant type pollution |
| 2. Assessment of the target pollutants concentration range | Determination of readily bioavailable, potentially bioavailable and unavailable pollutant fractions | |
| 3. Analysis of relevant environmental factors | Range of temperature, pH, redox potential, moiety, soil properties, etc. | |
| 4. Evaluation of nutrient levels | Potential limitation due to insufficient microelements, electron acceptors, etc. | |
| 5. Analysis of autochthonous microflora | Screening for native microbial consortia with the ability to either remove or mobilize the pollutant by producing biosurfactants | |
| II. Laboratory scale experiments | 1. Selection of appropriate bioremediators for conducting the bioremediation process | Microorganisms or plants which exhibit high tolerance toward target pollutants and distinct remediation potential (relevant catabolic genes, hyperaccumulative properties, etc.) |
| 2. Selection of additional amendments | Nutrients, co-inoculants, plant growth promoting microorganisms, arbuscular mycorrhizal fungi, etc. | |
| Laboratory scale feasibility studies for biosurfactant-supplementation, approach A: Addition of externally produced biosurfactants ( | 1. Selection of a biosurfactant and biosurfactant-producing microorganisms | Previous studies related to the topic or the native habitat of biosurfactant-producing microorganisms |
| 2. Assessment of potential biosurfactant-induced toxicity | EC50 values for relevant bioremediators towards biosurfactant only as well as biosurfactant-pollutant combinations; Analysis of microbial community dynamics as a response to the presence of biosurfactants | |
| 3. Evaluation of efficiency for biosurfactant-amended remediation | Increase in pollutant bioavailability, increased removal rate, short-term stimulation, enhanced biomass growth for the bioremediator | |
| 4. Determination of biosurfactant degradability | Biosurfactant not preferentially utilized compared to target pollutant, efficient usefulness period for short-term stimulation, time for re-introduction | |
| 5. Establishment of an optimal biosurfactant production method | Assessment of potential carbon sources for biosurfactant production (waste materials); optimization of the production process; Determination of whether crude biosurfactant-containing cultivation broth may be used or is purification necessary | |
| Laboratory scale feasibility studies for biosurfactant-supplementation, approach B: Stimulation of biosurfactant production on-site ( | 1. Selection of appropriate biosurfactant-producers | Preferentially – selection of biosurfactant-producing isolates from native microflora (autochthonous soil/marine microbes, rhizobacteria, etc.); Alternatively – use of non-producing isolates which may be genetically modified to secrete biosurfactants or application of microbial consortia with high bioaugmentation potential (high similarity between consortium members and autochthonous microorganisms). Both alternative approaches are subject to additional regulations |
| 2. Evaluation of biocompatibility between biosurfactant producers and the biofactor relevant for the treatment process | Lack of antagonistic interactions, simultaneous growth, increase in pollutant bioavailability, enhanced removal rate | |
| 3. Selection of an introduction method | Spraying of the whole cultivation broth with free-living cells or immobilization on appropriate carriers | |
| 4. Initial bioaugmentation tests | Satisfactory performance in terms of adaptability and survivability of the introduced biosurfactant-producers, no apparent shifts in microbial community dynamics, lack of antagonistic interactions with native microflora | |
| 5. Long-term ability to produce biosurfactants | Monitoring the level of biosurfactants upon bioaugmentation, the presence of relevant biosurfactant-associated genes after a certain period of time | |
| III. Field scale feasibility study | 1. Environmental response towards biosurfactants or biosurfactant-producers | Shifts in microbial populations; toxicity of biosurfactant to native organisms; adaptability and survivability of bioremediators and/or biosurfactant producers upon introduction; other potentially negative effects (i.e. uncontrolled mobilization of pollutants) |
| 2. Efficiency of treatment | Short-term and long-term removal of target pollutants in biosurfactant-amended treatment compared to control; duration | |
| 3. Evaluation of treatment feasibility | Justification of each treatment step; Potential efficiency enhancement vs. additional costs associated with biosurfactant-supplementation |