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黄色粘球菌中细胞形态发生的诱导。II. 大分子合成与诱导剂作用机制。

Induction of cellular morphogenesis in Myxococcus xanthus. II. Macromolecular synthesis and mechanism of inducer action.

作者信息

Sadler W, Dworkin M

出版信息

J Bacteriol. 1966 Apr;91(4):1520-5. doi: 10.1128/jb.91.4.1520-1525.1966.

Abstract

Sadler, William (University of Minnesota, Minneapolis), and Martin Dworkin. Induction of cellular morphogenesis in Myxococcus xanthus. II. Macromolecular synthesis and mechanism of inducer action. J. Bacteriol. 91:1520-1525. 1966.-Net changes in ribonucleic acid (RNA), deoxyribonucleic acid (DNA), and protein syntheses in cells of Myxococcus xanthus during induced, synchronous conversion to microcysts are described. The net synthesis of all three macromolecules was temporarily halted for a brief period during the initiation of shape change. Synthesis then resumed and leveled off when refractile microcysts began to appear. The conversion was completely sensitive, throughout the process, to low concentrations of chloramphenicol and actinomycin D. The uptake of amino acids and uracil was linear throughout the conversion, suggesting that the plateaus in rates of net synthesis of protein and RNA represented a period of rapid turnover. The most effective inducers of microcyst formation were fully saturated aliphatic compounds containing 2 to 4 carbon atoms and at least one primary or secondary alcohol group. Studies with labeled inducer indicated that the inducer need not be taken up by the cells to be effective, and probably interacts with some peripheral structure of the cell. The possibility that induction involves an alteration of a membrane-DNA complex is discussed.

摘要

萨德勒,威廉(明尼苏达大学,明尼阿波利斯),以及马丁·德沃金。黄色粘球菌细胞形态发生的诱导。II. 大分子合成与诱导剂作用机制。《细菌学杂志》91:1520 - 1525。1966年。——描述了黄色粘球菌细胞在诱导同步转化为微囊过程中核糖核酸(RNA)、脱氧核糖核酸(DNA)和蛋白质合成的净变化。在形态变化开始时,这三种大分子的净合成暂时停止了一段时间。然后当折射性微囊开始出现时,合成恢复并趋于平稳。在整个过程中,这种转化对低浓度的氯霉素和放线菌素D完全敏感。在整个转化过程中,氨基酸和尿嘧啶的摄取呈线性,这表明蛋白质和RNA净合成速率的平稳期代表了一个快速周转的时期。最有效的微囊形成诱导剂是含有2至4个碳原子且至少有一个伯醇或仲醇基团的完全饱和脂肪族化合物。用标记诱导剂进行的研究表明,诱导剂无需被细胞摄取就能发挥作用,并且可能与细胞的某些外周结构相互作用。讨论了诱导涉及膜 - DNA复合物改变的可能性。

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