期刊
ISME JOURNAL
卷 16, 期 10, 页码 2313-2319出版社
SPRINGERNATURE
DOI: 10.1038/s41396-022-01278-9
关键词
-
资金
- US Army Research Office [W911NF2010111]
- National Science Foundation/University of Southern California, Center for Dark Energy Biosphere Investigations [OCE-0939564]
- National Institutes of Health [R35-GM136412]
- U.S. Department of Defense (DOD) [W911NF2010111] Funding Source: U.S. Department of Defense (DOD)
Microorganisms finely coordinate catabolic and anabolic processes to optimize their fitness in varying environmental conditions. This study explores the system-level physiology of Methanococcus maripaludis, a methanogenic archaeon specialized in a specific niche, under phosphate limitation. The results show a decoupling of catabolism and anabolism, resulting in lower biomass yield compared to catabolically limited cells. Furthermore, the abundance of ribosomes and their biogenesis sectors exhibit a linear relationship with growth rate.
Catabolic and anabolic processes are finely coordinated in microorganisms to provide optimized fitness under varying environmental conditions. Understanding this coordination and the resulting physiological traits reveals fundamental strategies of microbial acclimation. Here, we characterized the system-level physiology of Methanococcus maripaludis, a niche-specialized methanogenic archaeon, at different dilution rates ranging from 0.09 to 0.003 h(-1) in chemostat experiments under phosphate (i.e., anabolic) limitation. Phosphate was supplied as the limiting nutrient, while formate was supplied in excess as the catabolic substrate and carbon source. We observed a decoupling of catabolism and anabolism resulting in lower biomass yield relative to catabolically limited cells at the same dilution rates. In addition, the mass abundance of several coarse-grained proteome sectors (i.e., combined abundance of proteins grouped based on their function) exhibited a linear relationship with growth rate, mostly ribosomes and their biogenesis. Accordingly, cellular RNA content also correlated with growth rate. Although the methanogenesis proteome sector was invariant, the metabolic capacity for methanogenesis, measured as methane production rates immediately after transfer to batch culture, correlated with growth rate suggesting translationally independent regulation that allows cells to only increase catabolic activity under growth-permissible conditions. These observations are in stark contrast to the physiology of M. maripaludis under formate (i.e., catabolic) limitation, where cells keep an invariant proteome including ribosomal content and a high methanogenesis capacity across a wide range of growth rates. Our findings reveal that M. maripaludis employs fundamentally different strategies to coordinate global physiology during anabolic phosphate and catabolic formate limitation.
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