Hespell R B
J Bacteriol. 1976 Nov;128(2):677-80. doi: 10.1128/jb.128.2.677-680.1976.
Selected enzyme activities were measured in extracts of the total cell pellets obtained at various times during aerobic intraperiplasmic growth of Bdellovibrio bacteriovorus 109J on anaerobically grown Escherichia coli substrate cells. Initially, the glycolytic enzyme activities were associated with the input of E. coli and the tricarboxylic acid cycle enzyme activities with the input of bdellovibrios. During the first 90 min of Bdellovibrio development, the glycolytic activities declined about 25 to 60%, whereas the tricarboxylic acid cycle activities increased about 10%. Between 110 and 180 min, the glycolytic activities decreased to trace levels and tricarboxylic acid cycle activities increased about 50 to 90%. Both bdellovibrio cell extracts and the cell-free growth menstruum (obtained after bdellovibrio growth on E. coli) caused the inactivation of glycolytic enzymes in E. coli extracts.
在食菌蛭弧菌109J于厌氧生长的大肠杆菌底物细胞上进行好氧周质内生长的不同时间所获得的全细胞沉淀提取物中,测定了选定的酶活性。最初,糖酵解酶活性与大肠杆菌的输入相关,三羧酸循环酶活性与蛭弧菌的输入相关。在蛭弧菌发育的最初90分钟内,糖酵解活性下降了约25%至60%,而三羧酸循环活性增加了约10%。在110至180分钟之间,糖酵解活性降至痕量水平,三羧酸循环活性增加了约50%至90%。蛭弧菌细胞提取物和无细胞生长培养液(在蛭弧菌在大肠杆菌上生长后获得)均导致大肠杆菌提取物中的糖酵解酶失活。