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首页> 外文期刊>Applied and Environmental Microbiology >Relationship of Intracellular Coenzyme F420 Content to Growth and Metabolic Activity of Methanobacterium bryantii and Methanosarcina barkeri
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Relationship of Intracellular Coenzyme F420 Content to Growth and Metabolic Activity of Methanobacterium bryantii and Methanosarcina barkeri

机译:细胞内辅酶F420含量与布鲁曼甲烷杆菌和巴氏甲烷球菌的生长及代谢活性的关系

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The use of F420 as a parameter for growth or metabolic activity of methanogenic bacteria was investigated. Two representative species of methanogens were grown in batch culture: Methanobacterium bryantii (strain M.o.H.G.) on H2 and CO2, and Methanosarcina barkeri (strain Fusaro) on methanol or acetate. The total intracellular content of coenzyme F420 was followed by high-resolution fluorescence spectroscopy. F420 concentration in M. bryantii ranged from 1.84 to 3.65 μmol · g of protein?1; and in M. barkeri grown with methanol it ranged from 0.84 to 1.54 μmol · g?1 depending on growth conditions. The content of F420 in M. barkeri was influenced by a factor of 2 depending on the composition of the medium (minimal or complex) and by a factor of 3 to 4 depending on whether methanol or acetate was used as the carbon source. A comparison of F420 content with protein, cell dry weight, optical density, and specific methane production rate showed that the intracellular content of F420 approximately followed the increase in biomass in both strains. In contrast, no correlation was found between specific methane production rate and intracellular F420 content. However, qCH4(F420), calculated by dividing the methane production rate by the coenzyme F420 concentration, almost paralleled qCH4(protein). These results suggest that F420 may be used as a specific parameter for estimating the biomass, but not the metabolic activity, of methanogens; hence qCH4(F420) determined in mixed populations with complex carbon substrates must be considered as measure of the actual methanogenic activity and not as a measure of potential activity.
机译:研究了使用F420作为产甲烷菌生长或代谢活性的参数。在分批培养中生长了两种代表性的产甲烷菌种:在H2和CO2上的蓝甲烷杆菌(M.o.H.G.菌株)和在甲醇或醋酸盐上的甲烷甲烷八叠球菌(Fusaro菌株)。辅酶F420的总细胞内含量随后是高分辨率荧光光谱法。 Bryantii中的F420浓度范围为1.84至3.65μmol·g蛋白?1;在甲醇条件下生长的巴克木(M. barkeri)的浓度范围为0.84至1.54μmol·g?1,具体取决于生长条件。根据培养基(最小或复杂)的成分,巴克氏杆菌中F420的含量受2因子的影响,而取决于是否使用甲醇或乙酸盐作为碳源,则受3到4因子的影响。将F420含量与蛋白质,细胞干重,光密度和特定甲烷生成速率进行比较,结果表明,两种菌株中F420的细胞内含量均大致随生物量的增加而变化。相反,在特定的甲烷产生速率和细胞内F420含量之间没有发现相关性。但是,用甲烷产生速率除以辅酶F420浓度计算得出的qCH4(F420)与qCH4(蛋白质)几乎平行。这些结果表明,F420可用作估计产甲烷菌生物量而不是代谢活性的特定参数。因此,在具有复杂碳底物的混合种群中测定的qCH4(F420)必须考虑为实际产甲烷活性的量度,而不是潜在活性的量度。

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