Acetate as a carbon source for hydrogen production by photosynthetic bacteria
Introduction
There are limited reserves of fossil fuels on Earth, and the combustion of the fuels leads to serious problems such as global climate changes. For this reason, much attention is presently being given to the development of clean, sustainable energy systems, with the potential to supplement and even substitute the fossil-fuel-based energy production. One of the alternatives, as an environmentally acceptable fuel, is molecular hydrogen. Hydrogen is a clean fuel yielding only water after combustion.
Photosynthetic bacteria can produce hydrogen at the expense of solar energy and small-chain organic acids as electron donors. The combination of photosynthetic bacteria with anaerobic bacteria can provide a system for hydrogen photoproduction from residual carbohydrates, e.g. from organic wastes (Mao et al., 1986, Sasaki, 1998). In such a system, anaerobic fermentation of organic wastes produces intermediates like low-molecular-weights organic acids in a first step, which are then converted to hydrogen by photosynthetic bacteria at the expense of light energy, in a second step. The conversion efficiency of light energy to hydrogen, with the supply of an appropriate carbon source, are the key factors for hydrogen production by biological systems (Hillmer and Gest, 1977).
The conversion of malate and lactate to hydrogen by photosynthetic bacteria is well documented (Zürrer and Bachofen, 1979, Kim et al., 1981, Kim et al., 1987, Miyake and Kawamura, 1987, Fascetti and Todini, 1995, Sasikala et al., 1997, Ike et al., 1997a, Ike et al., 1997b, Tsygankov et al., 1998). The main products of anaerobic fermentation are acetic and butyric acids (Segers et al., 1981). Little is known about the conversion of acetic and butyric acids to hydrogen by photosynthetic bacteria (Segers and Verstraete, 1983, Sasaki, 1998). The conversion of these acids would be advantageous in order to couple energy production with organic-waste treatment. The few works done, in which hydrogen production rates using different carbon sources were compared, reported lower hydrogen production rates with acetate and butyrate than with malate and/or lactate (Hillmer and Gest, 1977, Kim et al., 1980, Miyake et al., 1984, Sasaki, 1998).
The light efficiency is the other parameter that determines the feasibility of the biological-hydrogen production process. Only in a few studies light efficiencies have been reported (Miyake and Kawamura, 1987, Nakada et al., 1995, Nakada et al., 1996, El-Shishtawy et al., 1997, El-Shishtawy et al., 1998, Otsuki et al., 1998, Yamada et al., 1998). Among these studies, only Otsuki et al. (1998) used carbon sources other than malate or lactate (mixture of acetate, propionate and butyrate) and reported a light efficiency of 0.31%. So far, the highest reported efficiency of light to hydrogen conversion is 7.9%, with light from a solar simulator and lactate as electron donor (Miyake and Kawamura, 1987). However, this value was obtained at a small-scale experiment and with a low light intensity.
The energy conversion efficiencies and H2 production rates of three different photosynthetic bacteria under different light intensities and with different carbon sources are reported on here.
Section snippets
Photosynthetic bacteria
Rhodopseudomonas sp., culture number HCC 2037 (originally from the Mitsui-Miami collection with the Mitsui-number 22711), was kindly provided by Dr. Oscar Zaborsky from the University of Hawaii at Manoa, USA. R. palustris R1 was kindly provided by Dr. Toshi Otsuki from Ishikawajima-Harima Heavy Industries Co., Ltd, Yokohama, Japan. The non-identified photosynthetic strain was kindly provided by Dr Alfons Stams from the Laboratory of Microbiology, Wageningen University, The Netherlands. This
Carbon source
Four different carbon sources were used with the photosynthetic bacteria, Rhodopseudomonas sp., R. palustris and Microbiology strain. Lactate and malate were chosen, as they are the most widely used carbon sources for H2 production and, thus, can be used as a reference. The initial concentrations were taken from literature as those required for optimal H2 production (Sasikala et al., 1997, Eroglu et al., 1999). Acetate and butyrate were chosen as models of substrates of interest, as they are
Acknowledgements
The project was sponsored by the Dutch research program, Economy, Ecology and technology (KIEM 98013). Jorge M.S. Rocha thanks for the post doctoral fellowship PRAXIS XXI/BDP/18840/98 from Fundação para a Ciência e Tecnologia, Lisbon, Portugal. The authors thank Dr Toshi Otsuki, Dr Oscar Zaborsky and Dr Alfons Stams, respectively, for the supply of the strains R. palustris R1, Rhodopseudomonas sp. and the non-identified photosynthetic bacteria.
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