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一种在合成培养基中生长期间能够持续形成芽孢的枯草芽孢杆菌突变体的特性。

Properties of a Bacillus subtilis mutant able to sporulate continually during growth in synthetic medium.

作者信息

Endo T, Ishihara H, Freese E

出版信息

J Gen Microbiol. 1983 Jan;129(1):17-30. doi: 10.1099/00221287-129-1-17.

Abstract

Several mutants of Bacillus subtilis were isolated which sporulate continually during exponential growth in glucose medium. The spdA1 mutation, responsible for the continual sporulation of one of the mutants, mapped near thr. When an exponentially growing culture of a strain containing spdA1 was maintained at essentially constant turbidity, 5% of the viable cells contained heat-resistant spores. The continual sporulation depended on the stringent response since it was absent in spdA relA double mutants. Genetic and biochemical analysis indicated that the continual sporulation of spdA1 strains was associated with a lower specific activity of pyruvate carboxylase, which limited the rate of oxaloacetate synthesis from glucose via pyruvate and thereby the supply of compounds depending on the citrate cycle, especially aspartate. Therefore, the mild stringent response caused by the spdA1 mutation seems to result from a partial deficiency of aspartyl-tRNA which may exert its sporulation-initiating effect during a limited time interval in each growth cycle. A mutant blocked in fumarase activity (citG) behaved similarly. It grew only slowly in glucose medium because much of the limiting oxaloacetate was wasted for the excretion of fumarate. The mutant produced little aspartate and sporulated at a high frequency in glucose medium, even in the presence of glutamate; the sporulation was again prevented by aspartate or malate or by introduction of the relA marker into the strain.

摘要

分离出了几种枯草芽孢杆菌突变体,它们在葡萄糖培养基中指数生长期间持续形成芽孢。spdA1突变导致其中一个突变体持续产孢,该突变位于thr附近。当含有spdA1的菌株的指数生长培养物维持在基本恒定的浊度时,5%的活细胞含有耐热芽孢。持续产孢依赖于严谨反应,因为在spdA relA双突变体中不存在这种现象。遗传和生化分析表明,spdA1菌株的持续产孢与丙酮酸羧化酶的比活性较低有关,这限制了通过丙酮酸从葡萄糖合成草酰乙酸的速率,从而限制了依赖柠檬酸循环的化合物的供应,尤其是天冬氨酸。因此,spdA1突变引起的轻度严谨反应似乎是由于天冬氨酰-tRNA部分缺乏所致,这可能在每个生长周期的有限时间间隔内发挥其启动产孢的作用。一个延胡索酸酶活性受阻的突变体(citG)表现类似。它在葡萄糖培养基中生长缓慢,因为大量有限的草酰乙酸被浪费用于延胡索酸的排泄。该突变体产生很少的天冬氨酸,并且在葡萄糖培养基中即使存在谷氨酸也高频产孢;天冬氨酸或苹果酸或向菌株中引入relA标记再次阻止了产孢。

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