Design of new strategy for green algal photo-hydrogen production: Spectral-selective photosystem I activation and photosystem II deactivation
► A new strategy in photo-H2 production from green algae was successfully demonstrated. ► The new strategy is convenient because it only requires turning on and off PSI light. ► The PSI light (692nm) achieved initial photo-H2 production rate of 0.055mLH2mg−1Chlh−1. ► The PSI light (692nm) achieved m...
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Veröffentlicht in: | Bioresource technology 2012-09, Vol.120, p.233-240 |
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Sprache: | eng |
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Zusammenfassung: | ► A new strategy in photo-H2 production from green algae was successfully demonstrated. ► The new strategy is convenient because it only requires turning on and off PSI light. ► The PSI light (692nm) achieved initial photo-H2 production rate of 0.055mLH2mg−1Chlh−1. ► The PSI light (692nm) achieved maximal total hydrogen production of 0.108mLH2mg−1Chl. ► The new strategy shows promise of improved photo-H2 production through further optimization.
A new strategy in photosynthetic hydrogen (photo-H2) production from green algae was developed based on theory and successfully demonstrated. The new strategy applied a spectral-selective photosystem I (PSI) activating/photosystem II (PSII) deactivating radiation (or PSI light) that would drive a steady flow of electrons in the electron transport chain for delivery to hydrogenase for photo-H2 production, but would reduce oxygen production through water photolysis below the respiratory oxygen consumption so that an anoxic condition would be maintained as required by hydrogenase. Implementing the strategy by using a PSI light (692nm peak, 680–700nm) on Chlamydomonas reinhardtii cells resulted in relatively sustained photo-H2 production (total of 0.108mLH2mg−1Chl, exceeding 0.066mLH2mg−1Chl under white light). The strategy also proved successful and convenient in allowing cells to alternately switch between photo-H2 production and a recovery period by simply turning on or off the PSI light. |
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ISSN: | 0960-8524 1873-2976 |
DOI: | 10.1016/j.biortech.2012.06.011 |