Photobiological hydrogen production and nitrogenase activity in some heterocystous cyanobacteria

2001 ◽  
pp. 63-66 ◽  
Author(s):  
H. Masukawa ◽  
K. Nakamura ◽  
M. Mochimaru ◽  
H. Sakurai
1981 ◽  
Vol 36 (1-2) ◽  
pp. 87-92 ◽  
Author(s):  
Patrick C. Hallenbeck ◽  
Leon V. Kochian ◽  
John R. Benemann

Abstract Cultures of Anabaena cylindrica, grown on media containing 5 mᴍ NH4Cl (which represses heterocyst formation), evolved hydrogen after a period of dark incubation under an argon atmosphere. This hydrogen production was not due to nitrogenase activity, which was nearly undetectable, but was due to a hydrogenase. Cultures grown on media with tungsten substituted for molybdenum had a high frequency of heterocysts (15%) and inactive nitrogenase after nitrogen starvation. The hydrogenase activity of these cultures was three-fold greater than the activity of non-heterocystous cultures. The effects of oxygen inhibition on hydrogen evolution by hetero-cystous cultures suggest that two pools of hydrogenase activity exist - an oxygen sensitive hydrogen evolution in vegetative cells and a relatively oxygen-resistent hydrogen evolution in heterocysts. In either case, inhibition by oxygen was reversible. Light had an inhibitory effect on net hydrogen evolution. Hydrogen production in vitro was much higher than in vivo, indicating that in vivo hydrogenase activity is limited by endogenous reductant supply.


1983 ◽  
Vol 156 (3) ◽  
pp. 1118-1122 ◽  
Author(s):  
X K Zhang ◽  
J B Haskell ◽  
F R Tabita ◽  
C Van Baalen

2011 ◽  
Vol 36 (13) ◽  
pp. 7487-7499 ◽  
Author(s):  
Chris M. Yeager ◽  
Charles E. Milliken ◽  
Christopher E. Bagwell ◽  
Lauren Staples ◽  
Polly A. Berseth ◽  
...  

2010 ◽  
Vol 76 (13) ◽  
pp. 4293-4301 ◽  
Author(s):  
Hongtao Min ◽  
Louis A. Sherman

ABSTRACT We report on the hydrogen production properties of the unicellular, diazotrophic cyanobacterium Cyanothece sp. strain ATCC 51142. This organism has a versatile metabolism and can grow in the presence or absence of combined nitrogen and can grow photosynthetically or mixotrophically and heterotrophically in the presence of glycerol. The strain produces a bidirectional hydrogenase (encoded by the hox genes), an uptake hydrogenase (hupLS), and nitrogenase (nifHDK). We demonstrated hydrogen production by both the hydrogenase and the nitrogenase under appropriate metabolic conditions. The highest rates of hydrogen production were produced under nitrogen-fixing conditions when cells were grown and incubated under continuous light conditions, in either the presence or absence of glycerol. Under such nitrogen-fixing conditions, we have achieved rates of 300 μmol H2/mg chloramphenicol (Chl)/hr during the first 24 h of incubation. The levels of H2 measured were dependent upon the incubation conditions, such as sparging with argon, which generated anaerobic conditions. We demonstrated that the same conditions led to high levels of H2 production and N2 fixation, indicating that low-oxygen conditions favor nitrogenase activity for both processes. The levels of hydrogen produced by the hydrogenase are much lower, typically 5 to 10 μmol H2/mg Chl/hr. Hydrogenase activity was dependent upon electron transport through photosystem II (PS II), whereas nitrogenase activity was more dependent on PS I, as well as on respiration. Although cells do not double under the incubation conditions when sparged with argon to provide a low-oxygen environment, the cells are metabolically active, and hydrogen production can be inhibited by the addition of chloramphenicol to inhibit protein synthesis.


2017 ◽  
Vol 72 (3-4) ◽  
pp. 99-105
Author(s):  
Amal W. Danial ◽  
Ahmed M. Abdel Wahab ◽  
Houssam H. Arafat ◽  
Refat Abdel-Basset

Abstract Two local hydrogen-evolving strains of purple nonsulfur bacteria have been isolated, characterized, and identified as Rhodopseudomonas sp. TUT (strains Rh1 and Rh2). Lactate followed by succinate and malate supported the highest amounts of H2 production, growth (O.D.660nm, proteins and bacteriochlorphyll contents), nitrogenase activity, and uptake hydrogenase; the least of which was acetate. Alginate-immobilized cells evolved higher hydrogen amounts than free cell counterparts. Rh1 was more productive than Rh2 at all circumstances. Lactate-dependent hydrogen evolution was more than twice that of acetate, due to ATP productivity (2/–1, respectively), which is limiting to the nitrogenase activity. The preference of lactate over other acids indicates the feasibility of using these two strains in hydrogen production from dairy wastewater.


1978 ◽  
Vol 33 (7-8) ◽  
pp. 541-547 ◽  
Author(s):  
Hartmut Spiller ◽  
Anneliese Ernst ◽  
Wolfgang Kerfin ◽  
Peter Böger

Abstract Nittrogen-fixing cells of Nostoc muscorum grown under nitrogen or in the presence of nitrate exhibit substantial light-induced hydrogen production for over 15 hours in the presence of electron transport inhibitors. Rates attain levels of 12 μmol H2 evolved/ml packed cell volume and hour. The ATP-dependent nitrogenase, not a hydrogenase, is responsible for hydrogen production. This is indicated by poor sensitivity to CO and inhibition of the reaction by uncouplers, acetylene, and N2 . An active uptake hydrogenase minimizes light-induced H2 production. Although nitrogenase activity is somewhat decreased by several photosynthetic electron transport inhibitors, hydrogen production is markedly increased. This is due to lowering the partial pressure of oxygen in the cell, preventing oxidative hydrogen consumption.


2018 ◽  
Vol 84 (16) ◽  
Author(s):  
Jace Natzke ◽  
Jesse Noar ◽  
José M. Bruno-Bárcena

ABSTRACTAzotobacter vinelandiiselectively utilizes three types of nitrogenase (molybdenum, vanadium, and iron only) to fix N2, with their expression regulated by the presence or absence of different metal cofactors in its environment. Each alternative nitrogenase isoenzyme is predicted to have different electron flux requirements based onin vitromeasurements, with the molybdenum nitrogenase requiring the lowest flux and the iron-only nitrogenase requiring the highest. Here, prior characterized strains, derepressed in nitrogenase synthesis and also deficient in uptake hydrogenase, were further modified to generate new mutants lacking the ability to produce poly-β-hydroxybutyrate (PHB). PHB is a storage polymer generated under oxygen-limiting conditions and can represent up to 70% of the cells' dry weight. The absence of such granules facilitated the study of relationships between catalytic biomass and product molar yields across different adaptive respiration conditions. The released hydrogen gas observed during growth, due to the inability of the mutants to recapture hydrogen, allowed for direct monitoring ofin vivonitrogenase activity for each isoenzyme. The data presented here show that increasing oxygen exposure limits equally thein vivoactivities of all nitrogenase isoenzymes, while under comparative conditions, the Mo nitrogenase enzyme evolves more hydrogen per unit of biomass than the alternative isoenzymes.IMPORTANCEA. vinelandiihas been a focus of intense research for over 100 years. It has been investigated for a variety of functions, including agricultural fertilization and hydrogen production. All of these endeavors are centered aroundA. vinelandii's ability to fix nitrogen aerobically using three nitrogenase isoenzymes. The majority of research up to this point has targetedin vitromeasurements of the molybdenum nitrogenase, and robust data contrasting how oxygen impacts thein vivoactivity of each nitrogenase isoenzyme are lacking. This article aims to providein vivonitrogenase activity data using a real-time evaluation of hydrogen gas released by derepressed nitrogenase mutants lacking an uptake hydrogenase and PHB accumulation.


Sign in / Sign up

Export Citation Format

Share Document