Hungate R E, Smith W, Bauchop T, Yu I, Rabinowitz J C
J Bacteriol. 1970 May;102(2):389-97. doi: 10.1128/jb.102.2.389-397.1970.
An average of 11 (range, 2 to 47) mumoles of formate per g per hr was produced and used in whole bovine rumen contents incubated in vitro, as calculated from the product of the specific turnover rate constant, k, times the concentration of intercellular formate. The latter varied between 5 and 26 (average, 12) nmoles/g. The concentration of formate in the total rumen contents was as much as 1,000 times greater, presumably owing to formate within the microbial cells. The concentration of formate in rumen contents minus most of the plant solids was varied, and from the rates of methanogenesis the Michaelis constant, K(m), for formate conversion to CH(4) was estimated at 30 nmoles/g. Also, the dissolved H(2) was measured in relation to methane production, and a K(m) of 1 nmole/g was obtained. A pure culture of Methanobacterium ruminantium showed a K(m) of 1 nmole of H(2)/g, but the K(m) for formate was much higher than the 30 nmoles for the rumen contents. It is concluded that nonmethanogenic microbes metabolize intercellular formate in the rumen. CO(2) and H(2) are the principal substrates for rumen methanogenesis. Eighteen per cent of the rumen methane is derived from formate, as calculated from the intercellular concentration of hydrogen and formate in the rumen, the Michaelis constants for conversion of these substrates by rumen liquid, and the relative capacities of whole rumen contents to ferment these substrates.
通过将特定周转率常数k乘以细胞内甲酸浓度计算得出,在体外培养的整个牛瘤胃内容物中,每克每小时平均产生并利用11(范围为2至47)微摩尔的甲酸。后者在5至26(平均为12)纳摩尔/克之间变化。瘤胃总内容物中甲酸的浓度高达其1000倍,推测这是由于微生物细胞内的甲酸所致。去除大部分植物固体后的瘤胃内容物中甲酸浓度各不相同,根据甲烷生成速率,甲酸转化为CH₄的米氏常数K(m)估计为30纳摩尔/克。此外,还测量了与甲烷产生相关的溶解H₂,得到的K(m)为1纳摩尔/克。反刍甲烷杆菌的纯培养物显示H₂的K(m)为1纳摩尔/克,但甲酸的K(m)远高于瘤胃内容物的30纳摩尔。得出的结论是,非产甲烷微生物在瘤胃中代谢细胞内的甲酸。CO₂和H₂是瘤胃甲烷生成的主要底物。根据瘤胃中氢气和甲酸的细胞内浓度、瘤胃液转化这些底物的米氏常数以及整个瘤胃内容物发酵这些底物的相对能力计算得出,瘤胃中18%的甲烷来自甲酸。