Biochemical basis for carbon monoxide tolerance and butanol production by Butyribacterium methylotrophicum

被引:0
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作者
G.-J. Shen
J.-S. Shieh
A. J. Grethlein
M. K. Jain
J. G. Zeikus
机构
[1] MBI International,
[2] 3900 Collins Road,undefined
[3] Lansing,undefined
[4] MI 48910,undefined
[5] USA e-mail: zeikus@mbi.org Tel.: +1-517-337-3181 Fax: +1-517-332-7810,undefined
[6] Departments of Biochemistry and Microbiology,undefined
[7] Michigan State University,undefined
[8] 410 Biochemistry Building,undefined
[9] East Lansing,undefined
[10] MI 48824,undefined
[11] USA,undefined
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关键词
NADH; Butanol; Butyrate; Ethanol Production; Oxidoreductase;
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摘要
The biochemical mechanisms for growth tolerance to a 100% CO headspace in cultures, and butanol plus ethanol production from CO by Butyribacterium methylotrophicum were assessed in the wild-type and CO-adapted strains. The CO-adapted strain grew on glucose or CO under a 100% CO headspace, whereas, the growth of the wild-type strain was severely inhibited by 100% CO. The CO-adapted strain, unlike the wild-type, also produced butyrate, from either pyruvate or CO. The CO-adapted strain was a metabolic mutant having higher levels of ferredoxin–NAD oxidoreductase activity, which was not inhibited by NADH. Consequently, only the CO-adapted strain can grow on CO because CO oxidation generates reduced ferredoxin which, via the mutated ferredoxin–NAD reductase activity, forms reduced NADH required for catabolism. When the CO-adapted strain was grown at pH 6.0 it produced butanol (0.33 g/l) and ethanol (0.5 g/l) from CO and the cells contained the following NAD-linked enzyme activities (μmol min−1 mg protein−1): butyraldehyde dehydrogenase (227), butanol dehydrogenase (686), acetaldehyde dehydrogenase (82) and ethanol dehydrogenase (129).
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页码:827 / 832
页数:5
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