McCormick N G, Ordal E J, Whiteley H R
Department of Microbiology, University of Washington, Seattle, Washington.
J Bacteriol. 1962 Apr;83(4):899-906. doi: 10.1128/jb.83.4.899-906.1962.
McCormick, N. G. (University of Washington, Seattle), E. J. Ordal, and H. R. Whiteley. Degradation of pyruvate by Micrococcus lactilyticus. II. Studies of cofactors in the formate-exchange reaction. J. Bacteriol. 83:899-906. 1962.-Enzyme preparations from Micrococcus lactilyticus(2) are rendered inactive with respect to formate exchange by treatment with charcoal or Dowex-50, by dialysis, or by fractionation with ammonium sulfate. The activity may be completely restored by a "kochsaft" preparation (BES) obtained from M. lactilyticus and partially restored by similar BES preparations from Escherichia coli and Clostridium butyricum. Diphosphothiamine is required for formate exchange but full activity cannot be restored by known cofactors. Brief exposure to increased temperatures, air, extremes of pH, and absorption with charcoal and Dowex-50 decrease the cofactor activity of BES preparations. The addition of BES preparations from E. coli and Streptococcus faecalis causes a shift in the degradation of pyruvate by extracts of M. lactilyticus from the phosphoroclastic cleavage (to acetyl phosphate and formate) to the dismutation of pyruvate (to lactate, acetate, and carbon dioxide).C. cylindrosporum was found to mediate the formate-exchange reaction; the activity of crude extracts was stimulated by M. lactilyticus and C. butyricum BES preparations. M. lactilyticus BES also increased the formate-exchange activity of extracts of E. coli.
麦考密克,N.G.(华盛顿大学,西雅图),E.J.奥尔德尔和H.R.怀特利。乳酸微球菌对丙酮酸的降解作用。II. 甲酸交换反应中辅因子的研究。《细菌学杂志》83:899 - 906。1962年。——乳酸微球菌(2)的酶制剂经木炭或Dowex - 50处理、透析或硫酸铵分级分离后,在甲酸交换方面会失去活性。从乳酸微球菌获得的一种“kochsaft”制剂(BES)可使活性完全恢复,而从大肠杆菌和丁酸梭菌获得的类似BES制剂可部分恢复其活性。甲酸交换需要二磷酸硫胺素,但已知的辅因子无法使活性完全恢复。短暂暴露于升高的温度、空气、极端pH值以及经木炭和Dowex - 50吸附会降低BES制剂的辅因子活性。添加来自大肠杆菌和粪链球菌的BES制剂会使乳酸微球菌提取物对丙酮酸的降解从磷酸裂解(生成乙酰磷酸和甲酸)转变为丙酮酸的歧化反应(生成乳酸、乙酸和二氧化碳)。发现柱状柱孢菌可介导甲酸交换反应;粗提取物的活性受到乳酸微球菌和丁酸梭菌BES制剂的刺激。乳酸微球菌BES也增加了大肠杆菌提取物的甲酸交换活性。