Baresi L
J Bacteriol. 1984 Oct;160(1):365-70. doi: 10.1128/jb.160.1.365-370.1984.
Cell lysates of acetate-grown Methanosarcina barkeri 227 were found to cleave acetate to CH4 and CO2. The aceticlastic reaction was identified by using radioactive methyl-labeled acetate. Cell lysates decarboxylated acetate in a nitrogen atmosphere, conserving the methyl group in methane. The rate of methanogenesis from acetate in the cell lysates was comparable to that observed with whole cells. Aceticlastic activity was found in the particulate fraction seperate from methylcoenzyme M methylreductase activity, which occurs in the soluble fraction. Pronase treatment eliminated methylcoenzyme M methylreductase activity in lysates and stimulated aceticlastic activity, indicating the aceticlastic activity was not derived from unbroken cells, which are unaffected by proteolytic treatment.
研究发现,以乙酸盐为生长底物的巴氏甲烷八叠球菌227的细胞裂解物可将乙酸盐裂解为甲烷和二氧化碳。通过使用放射性甲基标记的乙酸盐确定了乙酸裂解反应。细胞裂解物在氮气氛围中使乙酸盐脱羧,将甲基保留在甲烷中。细胞裂解物中由乙酸盐产生甲烷的速率与完整细胞的观测速率相当。乙酸裂解活性存在于与甲基辅酶M甲基还原酶活性分离的颗粒部分,而甲基辅酶M甲基还原酶活性存在于可溶部分。蛋白酶处理消除了裂解物中的甲基辅酶M甲基还原酶活性并刺激了乙酸裂解活性,这表明乙酸裂解活性并非来自未破碎的细胞,因为未破碎的细胞不受蛋白水解处理的影响。