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大肠杆菌中的限氧连续培养与呼吸能量守恒

Oxygen-limited continuous culture and respiratory energy conservation in Escherichia coli.

作者信息

Rice C W, Hempfling W P

出版信息

J Bacteriol. 1978 Apr;134(1):115-24. doi: 10.1128/jb.134.1.115-124.1978.

Abstract

Escherichia coli B was cultured continuously in succinate-minimal medium under conditions of oxygen limitation in the phauxostat. With decreasing oxygenation and consequent decreasing growth rates, the complement of terminal cytochrome oxidases changed as follows: high growth rates, cytochrome o; intermediate growth rates, cytochromes o and d; lowest growth rates, cytochromes o, d, and a1. Respiratory kinetics exhibited by nongrowing cell suspensions obtained from continuous cultures indicated that terminal oxidase activity was exhibited by cytochrome o (Km for O2 = 0.2 micron; Vmax = 1.1 to 1.5 mumol of O2 per nmol of cytochrome o per min) and cytochrome d (Km for O2 = 0.024 micron; Vmax = 0.7 mumol of O2 per nmol of cytochrome d per min). During oxygen-limited growth, the molar growth yield referred to respiration, and corrected for maintenance respiration [Yo(max)], was 12.6 g (dry weight) per g-atom of oxygen, not significantly different from the succinate-limited value of 12.0 g (dry weight) per g-atom of oxygen. The rate of maintenance respiration of the oxygen-limited culture was only 3.4 mg-atoms of O per g (dry weight) per h, some threefold less than that of the succinate-limited culture. Respiration-driven proton extrusion did not vary with the growth rate or with the complement of terminal oxidases (H+/O = 3.7; standard deviation, 0.07). We conclude that the content of terminal oxidases is without effect on the efficiency of respiratory energy conservation.

摘要

在限氧条件下,将大肠杆菌B在琥珀酸盐基本培养基中于恒化器中连续培养。随着氧合作用降低以及随之而来的生长速率下降,末端细胞色素氧化酶的组成发生如下变化:高生长速率时,细胞色素o;中等生长速率时,细胞色素o和d;最低生长速率时,细胞色素o、d和a1。从连续培养物中获得的非生长细胞悬液所表现出的呼吸动力学表明,末端氧化酶活性由细胞色素o(O2的Km = 0.2微米;Vmax = 每分钟每nmol细胞色素o 1.1至1.5 μmol O2)和细胞色素d(O2的Km = 0.024微米;Vmax = 每分钟每nmol细胞色素d 0.7 μmol O2)表现出来。在限氧生长期间,以呼吸作用为参照并校正维持呼吸后的摩尔生长产量[Yo(max)]为每克原子氧12.6克(干重),与琥珀酸盐限制条件下每克原子氧12.0克(干重)的值无显著差异。限氧培养物的维持呼吸速率仅为每克(干重)每小时3.4毫克原子氧,约为琥珀酸盐限制培养物的三分之一。呼吸驱动的质子外排不随生长速率或末端氧化酶的组成而变化(H+/O = 3.7;标准偏差,0.07)。我们得出结论,末端氧化酶的含量对呼吸能量保存效率没有影响。

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