Open AccessMeasurement and modeling of multiple substrate oxidation by methanotrophs at 20 °C
Author(s) -
Yoon Sukhwan,
Semrau Jeremy D.
Publication year - 2008
Publication title -
fems microbiology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1111/j.1574-6968.2008.01314.x
Subject(s) - methane monooxygenase , trichloroethylene , chemistry , vinyl chloride , methanotroph , degradation (telecommunications) , methane , biochemistry , substrate (aquarium) , enzyme , anaerobic oxidation of methane , environmental chemistry , biology , organic chemistry , ecology , telecommunications , computer science , copolymer , polymer
Earlier experiments have shown that when Methylosinus trichosporium OB3b was grown at 30 °C, greater growth and degradation of chlorinated ethenes was observed under particulate methane monooxygenase (pMMO)‐expressing conditions than sMMO‐expressing conditions. The effect of temperature on the growth and ability of methanotrophs to degrade chlorinated ethenes, however, has not been examined, particularly temperatures more representative of groundwater systems. Thus, experiments were performed at 20 °C to examine the effect of mixtures of trichloroethylene, trans ‐dichloroethylene and vinyl chloride in the presence of methane on the growth and ability of Methylosinus trichosporium OB3b cells to degrade these pollutants. Although the maximal rates of chlorinated ethane degradation were greater by M. trichosporium OB3b expressing sMMO as compared with the same cell expressing pMMO, the growth and ability of sMMO‐expressing cells to degrade these cosubstrates was substantially inhibited in their presence as compared with the same cell expressing pMMO. The Δ model developed earlier was found to be useful for predicting the effect of chlorinated ethenes on the growth and ability of M. trichosporium OB3b to degrade these compounds at a growth temperature of 20 °C. Finally, it was also discovered that at 20 °C, cells expressing pMMO exhibited faster turnover of methane than sMMO‐expressing cells, unlike that found earlier at 30 °C, suggesting that temperature may exert selective pressure on methanotrophic communities to express sMMO or pMMO.