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Organism

Organism. H 2 μmol/ mg drywt/h. Growth conditions. H2 evolution assay conditions. Anabaena cylindrica B-629. 0.103. Air + CO 2 (5%); 7000 lx at the, surface of the culture vessels. Ar + CO 2 (3%); 4000 lx at the surface of the culture vessels. Oscillatoria brevis B-1567. 0.168.

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Organism

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  1. Organism H2 μmol/ mgdrywt/h Growth conditions H2 evolution assay conditions Anabaena cylindrica B-629 0.103 Air + CO2 (5%); 7000 lx at the, surface of the culture vessels Ar + CO2 (3%); 4000 lx at the surface of the culture vessels Oscillatoria brevis B-1567 0.168 Air + CO2 (5%); 7000 lx at the surface of the culture vessels Ar + CO2 (3%); 4000 lx at the surface of the culture vessels Calothrix scopulorum 1410=5 0.128 Air + CO2 (5%); 7000 lx at the surface of the culture vessels Ar + CO2 (3%); 4000 lx at the surface of the culture vessels Calothrix membranacea B-379 0.108 Air + CO2 (5%); 7000 lx at the surface of the culture vessels Ar + CO2 (3%); 4000 lx at the surface of the culture vessels

  2. Organism Maximum hydrogen evolution Growth conditions H2 evolution assay conditions Anabaena sp. N-7363 36 μmol/mg chl a/h - Ar Anabaena variabilis PK84 167.60 μmol/mg chl a/h Ar(73%) + N2(25%) + CO2(2%); 90µE m2s-1 Ar(93%) + N2(5%) + CO2(2%); 90 µE m2s-1 Anabaena variabilis PK17R 59.18 μmol/mg chl a/h Ar(73%) + N2(25%) + CO2(2%); 90 µE m2s-1 Ar(93%) + N2(5%) + CO2(2%); 90 µE m2s-1 Anabaena variabilis AVM13 68 μmol/mg chl a/h Air + CO2(1%); 100 µE m2s-1 -

  3. Organism used - Rhodobacter sphareroides Medium used – asy medium Culture was harvested - 4000 rpm for 20mins Cultivated in gl medium [10 mM sodium glutamate 83 mMsodium lactate 1.5 mMsodium hydrogen carbonate ] Outcome Hydrogen production After hydrogen production was detected the culture was changed to gl medium with FeSO4 limitation

  4. Photo fermentation for malate for hydrogen production

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