Literature DB >> 16346205

Nitrogenase activity (acetylene reduction) of root-associated, cold-climate azospirillum, enterobacter, Klebsiella, and pseudomonas species during growth on various carbon sources and at various partial pressures of oxygen.

K Haahtela1, K Kari, V Sundman.   

Abstract

A comprehensive view of the diazotrophic bacterial flora of plants requires that attention be paid to the appropriate carbon and oxygen requirements during isolation of the bacteria. Twenty compounds (monosaccharides, disaccharides, polyols, and organic acids) were therefore examined as carbon and energy sources for nitrogenase activity in semisolid stab cultures at pO(2) values of 0.21, 0.02, and </=0.002 with 12 strains of diazotrophic root-associated bacteria. With the facultatively anaerobic bacteria of the genera Klebsiella and Enterobacter, the best substrate was sucrose, followed by fructose and mannitol, whereas among the organic acids, only malic and fumaric acids supported any activity. With the obligately aerobic bacteria of the genera Azospirillum and Pseudomonas, disaccharides were not utilized for nitrogen fixation, but several organic acids were accepted in addition to monosaccharides and polyols; malate and glucose were the best substrates. The patterns of the carbon sources utilized for nitrogen fixation were coherent within the species, with the exception of one Klebsiella pneumoniae and one Enterobacter agglomerans strain, both isolated from the same individual grass plant, which were unable to utilize lactose. Anaerobic conditions (pO(2) value of </=0.002) were required for maximum nitrogenase activity with the facultatively anaerobic bacteria, with the exception of one strain of E. agglomerans, which required atmospheric oxygen (pO(2) value of 0.21). Also, the obligately aerobic diazotrophs required atmospheric oxygen for maximum nitrogenase activity. The maximum specific nitrogenase activities (expressed as micromoles of C(2)H(4) . milligram of bacterial protein . hour) noted during the exponential growth phase of the bacteria were the following: 2.68 with Azospirillum lipoferum on malate, 2.41 with K. pneumoniae and 1.58 with E. agglomerans on sucrose, and 0.95 with Pseudomonas sp. on malate.

Entities:  

Year:  1983        PMID: 16346205      PMCID: PMC242324          DOI: 10.1128/aem.45.2.563-570.1983

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  14 in total

1.  Root-associated n(2) fixation (acetylene reduction) by enterobacteriaceae and azospirillum strains in cold-climate spodosols.

Authors:  K Haahtela; T Wartiovaara; V Sundman; J Skujiņs
Journal:  Appl Environ Microbiol       Date:  1981-01       Impact factor: 4.792

2.  A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples.

Authors:  M A Markwell; S M Haas; L L Bieber; N E Tolbert
Journal:  Anal Biochem       Date:  1978-06-15       Impact factor: 3.365

3.  Factors affecting growth and nitrogen fixation of Spirillum lipoferum.

Authors:  Y Okon; S L Albrecht; R H Burris
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

4.  Nitrogen fixation by Klebsiella grown in the presence of oxygen.

Authors:  R Klucas
Journal:  Can J Microbiol       Date:  1972-12       Impact factor: 2.419

5.  Growth of Spirillum lipoferum at constant partial pressures of oxygen, and the properties of its nitrogenase in cell-free extracts.

Authors:  Y Okon; J P Houchins; S L Albrecht; R H Burris
Journal:  J Gen Microbiol       Date:  1977-01

6.  Ecological distribution of Spirillum lipoferum Beijerinck.

Authors:  J Dobereiner; I E Marriel; M Nery
Journal:  Can J Microbiol       Date:  1976-10       Impact factor: 2.419

7.  An asymbiotic nitrogen-fixing bacterium from the root environment of corn.

Authors:  P N Raju; H J Evans; R J Seidler
Journal:  Proc Natl Acad Sci U S A       Date:  1972-11       Impact factor: 11.205

8.  Effect of oxygen and nitrate on nitrogen fixation and denitrification by Azospirillum brasilense grown in continuous culture.

Authors:  L M Nelson; R Knowles
Journal:  Can J Microbiol       Date:  1978-11       Impact factor: 2.419

9.  A taxonomic study of the Spirillum lipoferum group, with descriptions of a new genus, Azospirillum gen. nov. and two species, Azospirillum lipoferum (Beijerinck) comb. nov. and Azospirillum brasilense sp. nov.

Authors:  J J Tarrand; N R Krieg; J Döbereiner
Journal:  Can J Microbiol       Date:  1978-08       Impact factor: 2.419

10.  The apparent ATP requirement for nitrogen fixation in growing Klebsiella pneumoniae.

Authors:  S Hill
Journal:  J Gen Microbiol       Date:  1976-08
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  7 in total

1.  Quantification of frankia strains and other root-associated bacteria in pure cultures and in the rhizosphere of axenic seedlings by high-performance liquid chromatography-based muramic Acid assay.

Authors:  R Rönkkö; T Pennanen; A Smolander; V Kitunen; H Kortemaa; K Haahtela
Journal:  Appl Environ Microbiol       Date:  1994-10       Impact factor: 4.792

2.  In vitro adhesion of n(2)-fixing enteric bacteria to roots of grasses and cereals.

Authors:  K Haahtela; T K Korhonen
Journal:  Appl Environ Microbiol       Date:  1985-05       Impact factor: 4.792

3.  Influence of different factors on the nitrogenase activity of the engineered Escherichia coli 78-7.

Authors:  Li-hong Zhang; San-feng Chen
Journal:  World J Microbiol Biotechnol       Date:  2015-04-08       Impact factor: 3.312

4.  The Mexican giant maize of Jala landrace harbour plant-growth-promoting rhizospheric and endophytic bacteria.

Authors:  Bibiana Rios-Galicia; Catalina Villagómez-Garfias; Esaú De la Vega-Camarillo; Jairo Eder Guerra-Camacho; Nora Medina-Jaritz; Ramón Ignacio Arteaga-Garibay; Lourdes Villa-Tanaca; César Hernández-Rodríguez
Journal:  3 Biotech       Date:  2021-09-24       Impact factor: 2.893

5.  Nitrogen-fixing and uricolytic bacteria associated with the gut of Dendroctonus rhizophagus and Dendroctonus valens (Curculionidae: Scolytinae).

Authors:  Jesús Morales-Jiménez; Arturo Vera-Ponce de León; Aidé García-Domínguez; Esperanza Martínez-Romero; Gerardo Zúñiga; César Hernández-Rodríguez
Journal:  Microb Ecol       Date:  2013-03-24       Impact factor: 4.552

6.  Catabolism of carbohydrates and organic acids and expression of nitrogenase by azospirilla.

Authors:  G Martinez-Drets; M Del Gallo; C Burpee; R H Burris
Journal:  J Bacteriol       Date:  1984-07       Impact factor: 3.490

7.  Feeding Formula Eliminates the Necessity of Bacterial Dysbiosis and Induces Inflammation and Injury in the Paneth Cell Disruption Murine NEC Model in an Osmolality-Dependent Manner.

Authors:  Shiloh R Lueschow; Stacy L Kern; Huiyu Gong; Justin L Grobe; Jeffrey L Segar; Susan J Carlson; Steven J McElroy
Journal:  Nutrients       Date:  2020-03-26       Impact factor: 5.717

  7 in total

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