Genomes of rumen bacteria encode atypical pathways for fermenting hexoses to short-chain fatty acids
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ArticleKAUST Department
Red Sea Research Center (RSRC)Date
2017-11-02Online Publication Date
2017-11-02Print Publication Date
2017-11Permanent link to this record
http://hdl.handle.net/10754/625456
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Show full item recordAbstract
Bacteria have been thought to follow only a few well-recognized biochemical pathways when fermenting glucose or other hexoses. These pathways have been chiseled in the stone of textbooks for decades, with most sources rendering them as they appear in the classic 1986 text by Gottschalk. Still, it is unclear how broadly these pathways apply, given that they were established and delineated biochemically with only a few model organisms. Here we show that well-recognized pathways often cannot explain fermentation products formed by bacteria. In the most extensive analysis of its kind, we reconstructed pathways for glucose fermentation from genomes of 48 species and subspecies of bacteria from one environment (the rumen). In total, 44% of these bacteria had atypical pathways, including several that are completely unprecedented for bacteria or any organism. In detail, 8% of bacteria had an atypical pathway for acetate formation; 21% for propionate or succinate formation; 6% for butyrate formation; and 33% had an atypical or incomplete Embden-Meyerhof-Parnas pathway. This study shows that reconstruction of metabolic pathways-a common goal of omics studies-could be incorrect if well-recognized pathways are used for reference. Further, it calls for renewed efforts to delineate fermentation pathways biochemically. This article is protected by copyright. All rights reserved.Citation
Hackmann TJ, Ngugi DK, Firkins JL, Tao J (2017) Genomes of rumen bacteria encode atypical pathways for fermenting hexoses to short-chain fatty acids. Environmental Microbiology. Available: http://dx.doi.org/10.1111/1462-2920.13929.Sponsors
We thank G. Suen (University of Wisconsin-Madison), A. Neumann (University of Wisconsin-Madison), and P. Weimer (USDA-ARS, Madison, WI) for conservations on missing pyruvate kinase in Fibrobacter. We also thank S. Hackmann (University of Florida) for reviewing the manuscript. This work was supported by U.S. Department of Agriculture (USDA) National Institute of Food and Agriculture (NIFA) Hatch Project FLA-ANS-005307 and USDA-NIFA Hatch/Multi-State Project FLA-ANS-005304.Publisher
WileyJournal
Environmental MicrobiologyPubMed ID
28892251Additional Links
http://onlinelibrary.wiley.com/doi/10.1111/1462-2920.13929/abstractae974a485f413a2113503eed53cd6c53
10.1111/1462-2920.13929
Scopus Count
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