Photoheterotrophic Hydrogen Production of Rhodobacter sphaeroides KCTC 1434 under Alternating Ar and N2 Headspace Gas
Ruby Lynn G. Ventura1*, Jey-R S. Ventura2, and Young-Sook Oh3
1Rural High School, College of Arts and Science, University of the
Philippines Los Baños, Paciano Rizal, Bay 4033 Laguna, Philippines
2Department of Engineering Science, College of Engineering and Agro-
Industrial Technology, University of the Philippines Los Baños, College,
Los Baños 4031 Laguna, Philippines
3Department of Environmental Engineering and Energy, Myongji University,
116 Myongji-Ro, Cheoin-Gu, Yongin, Gyeonggi-Do 449-728 Republic of Korea
*Corresponding author: This email address is being protected from spambots. You need JavaScript enabled to view it.
ABSTRACT
In this paper, the effect of switching argon (Ar) and nitrogen (N2) headspace gases during the onset of photofermentative H2 production on butyrate and propionate was studied using Rhodobacter sphaeroides KCTC 1434. Reactor headspace were initially purged with N2 in the first set-up, while Ar was used in the second set-up. After 60 h, the first set of reactors were repurged with N2 (PN2R, BN2R); while the second set were replaced with Ar (PArR, BArR). Results showed that replacement with N2 automatically decreased H2 productivity in propionate and butyrate by 5.5 and 4.0 times, respectively. Replacement with N2 led to changes in cell densities and increased final pH in the culture medium. On the other hand, initial exposure to N2 and subsequent re-purging with Ar significantly increased (p = 7.87 x 10–10) cell weight and delayed entry of the strain to stationary phase of cell growth. H2 production lag times were determined to be 144 h for PArR (Substrate conversion efficiency, SCE = 96.63%) and 172 h for BArR (SCE = 55.60%). Exposure to any of the gases did not bring significant difference in substrate consumption. Overall, the investigation showed that utilizing N2-to-Ar headspace purging is feasible in photofermentation setup. Further exploration involving pH control and quantification of ammonia (NH3) and polyhydroxybutyrate (PHB) may be carried to extend the use of this setup in a photofermentation system.
INTRODUCTION
The worldwide dependency on fossil fuel has created the aggravation of global warming by greenhouse gas emission from combustion products. This reliance on fossil-based fuel leads to significant depletion of buried combustible geologic deposits (Chandrasekhar et al. 2015) and makes the global economy immensely vulnerable to the state of petroleum industry. Scientific endeavors are engaged in developing alternative energy sources to replace fossil fuel. Among these alternatives, H2 offers a tremendous potential as a clean and renewable energy currency. Unlike other alternative fuels, the combustion of H2 produces water instead of CO2 and other carbon-based emissions. H2 energy yield (122 kJ/g) is greater . . . . read more
REFERENCES
ABO-HASHESH M, DESAUNAY N, HALLENBECK PC. 2013. High yield single state conversion of glucose to hydrogen by photofermentation with continuous culture of Rhodobacter capsulatus JP91. Bioresource Technology 128: 513–517.
ARREGI A, AMUTIO M, LOPEZ G, BILBAO J, OLAZAR M. 2018. Evaluation of thermochemical routes for hydrogen production from biomass: A review. Energy Conversion and Management 165: 696–719.
CHANDRASEKHAR K, LEE Y-J, LEE D-W. 2015. Biohydrogen Production: Strategies to Improve Process Efficiency through Microbial Routes. International Journal of Molecular Sciences 16(4): 8266–93.
EROGLU I, ASLAN K, GÜNDÜZ U, YÜCEL M. TÜRKER L. 1999. Substrate consumption rates for hydrogen production by Rhodobacter sphaeroides in a column photobioreactor. Journal of Biotechnology 70: 103–113.
FANG HHP, LIU H, ZHANG T. 2005. Phototrophic hydrogen production from acetate and butyrate in wastewater. International Journal of Hydrogen Energy 30: 785–793.
GOLOMYSOVA A, GOMELSKY M, IVANOV PS. 2010. Flux balance analysis of photoheterotrophic growth of purple nonsulfur bacteria relevant to biohydrogen production. International Journal of Hydrogen Energy 35: 12751–60.
GHOSH D, SOBRO IF, HALLENBECK PC. 2012. Stoichiometric conversion of biodiesel derived from crude glycerol to hydrogen: Response surface methodology study of the effects of light intensity and crude glycerol and glutamate concentration. Bioresource Technology 106: 154–160.
HÄDICKE O, GRAMMEL H, KLAMT S. 2011. Metabolic network modeling of redox balancing and biohydrogen production in purple nonsulfur bacteria. BMC Systems Biology 5: 150.
HILLMER P, GEST H. 1977a. H2 Metabolism in the photosynthetic bacterium Rhodopseudomonas capsulata: H2 production by growing cultures. Journal of Bacteriology 129(2): 724–731.
HILLMER P, GEST H. 1977b. H2 metabolism in the photosynthetic bacterium Rhodopseudomonas capsulata: Production and utilization of H2 by resting cells. Journal of Bacteriology 129(2): 732–739.
HUANG JJ, HEINIGER EK, McKINLAY JB, HARWOOD CS. 2010. Production of Hydrogen Gas from Light and the Inorganic Electron Donor Thiosulfate by Rhodopseudomonas palustris. Applied and Environmental Microbiology 76(23): 7717–22.
JARUNGLUMLERT T, PROMMUAK C, PUTMAI N, PAVASANT P. 2017. Scaling-up bio-hydrogen production from food waste: Feasibilities and challenges. International Journal of Hydrogen Energy 43: 634–648.
KAPDAN I, KARGI F, OZTEKIN R, ARGUN H. 2009. Bio-hydrogen production from acid hydrolyzed wheat starch by photo-fermentation using different Rhodobacter sp. International Journal of Hydrogen Energy 34: 2201–07.
KARS G, GÜNDÜZ U. 2010. Towards a super H2 producer: Improvements in photofermentative biohydrogen production by genetic manipulations. International Journal of Hydrogen Energy 35: 6646–56.
KHATIPOV E, MIYAKE M, MIYAKE J, ASADA Y. 1998. Accumulation of poly-β-hydroxybutyrate by Rhodobacter sphaeroides on various carbon and nitrogen substrates. FEMS Microbiology Letters 162: 39–45.
KIM M, KIM D, CHA J. 2012a. Culture conditions affecting H2 production by phototrophic bacterium Rhodobacter sphaeroides KD131. International Journal of Hydrogen Energy 37: 14055–61.
KIM M, KIM D, CHA J, LEE JK. 2012b. Effect of carbon and nitrogen sources on photo-fermentative H2 production associated with nitrogenase, uptake hydrogenase activity, and PHB accumulation in Rhodobacter sphaeroides KD131. Bioresource Technology 116: 179–183.
KIRTAY E. 2011. Recent advances in production of hydrogen from biomass. Energy Conversion and Management 52: 1778–89.
KOKU H, EROĞLU İ, GÜNDÜZ U, YÜCEL M, TÜRKER L. 2002. Aspects of the metabolism of hydrogen production by Rhodobacter sphaeroides. International Journal of Hydrogen Energy 27: 1315–29.
LIU H, GROT S, LOGAN BE. 2005. Electrochemically assisted microbial production of hydrogen from acetate. Environmental Science and Technology 39: 4317–20.
LIU Y, GHOSH D, HALLENBECK PC. 2015. Biological reformation of ethanol to hydrogen by Rhodopseudomonas palustris CGA009. Bioresource Technology 102: 8557–68.
MADIGAN M, COS S, STEGEMAN R. 1984. Nitrogen fixation and nitrogenase activities in members of the family Rhodospirillaceae. Journal of Bacteriology 157(1): 73–78.
MELNICKI M, BIANCHI L, DE PHILIPPIS R, MELIS A. 2008. Hydrogen Production during the stationary phase in Purple Photosynthetic Bacteria. International Journal of Hydrogen Energy 33: 6525–34.
NYSTROM T. 2004. Stationary phase Physiology. Annual Review of Microbiology 58: 161–181.
PANDEY A, SRIVASTAVA N, SINH P. 2012. Optimization of hydrogen production by Rhodobacter sphaeroides NMBL-01. Biomass and Bioenergy 32: 251–256.
POOLE P, DILWORTH MJ, GLENN AR. 1987. Ammonia is the preferred nitrogen source in several rhizobia. Journal of General Microbiology 133: 1707–12.
RAHMAN SNA, MASDAR MS, ROSI MI, MAJLAN EH, HUSAINI T. 2015. Overview of Biohydrogen Production Technologies and Application in Fuel Cell. American Journal of Chemistry 5(3A): 13–23.
RAMACHANDRAN R, MENON RK. 1998. An overview of industrial uses of hydrogen. International Journal of Hydrogen Energy 23: 593–598.
REY F, HEINIGER E, HARWOOD C. 2007. Redirection of metabolism for biological hydrogen production. Appl. Environ. Microbiol. 73(5): 1665–71.
RYU M-H, HULL NC, GOMELSKY M. 2014. Metabolic engineering of Rhodobacter sphaeroides for improved hydrogen production. International Journal of Hydrogen Energy 39: 6384–90.
SAGNAK R, KARGI F. 2011. Photo-fermentative hydrogen gas production from dark fermentation effluent of acid hydrolyzed wheat starch with periodic feeding. International Journal of Hydrogen Energy 36: 4348–53.
SASIKALA K, RAMANA CV, RAGHUVEER RAO P, SUBRAHMANYAM M. 1990. Effect of gas phase on the photoproduction of hydrogen and substrate conversion efficiency in the photosynthetic bacterium Rhodobacter sphaeroides O.U. 001. International Journal of Hydrogen Energy 15: 795–797.
STEPHEN AJ, ARCHER SA, OROZCO RL, MACASJIE LE. 2017. Advances and bottlenecks in microbial hydrogen production 10(5): 1120–27.
UYAR B, EROGLU I, YΫCEL M, GΫNDΫZ U. 2009. Photofermentative hydrogen production from volatile fatty acids present in dark fermentation effluents. International Journal of Hydrogen Energy 34: 4517–23.
VENTURA RLG, VENTURA JS, OH Y-S. 2016. Investigation of the Photoheterotrophic Hydrogen Production of Rhodobacter sphaeroides KCTC 1434 using Volatile Fatty Acids under Argon and Nitrogen Headspace. American Journal of Environmental Sciences 12(6): 358–369.
XIAO N, CHEN Y, CHEN A, FENG L. 2014. Enhanced Bio-hydrogen Production from Protein Wastewater by Altering Protein Structure and Amino Acids Acidification Type. Scientific Reports 4: 3992.
YANG H, ZHANG J, WANG X, JIANGTAO F, YAN W, LIEJIN G. 2014. A newly isolated Rhodobacter sphaeroides with high hydrogen production performance. International Journal of Hydrogen Energy 39(19): 10051–60.