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Synthesis of peptidoglycan and membrane during the division cycle of rod-shaped, gram-negative bacteria.

机译:在杆状革兰氏阴性细菌分裂过程中肽聚糖和膜的合成。

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摘要

A modified procedure for determining the pattern of peptidoglycan synthesis during the division cycle has allowed the measurement of the rate of side wall synthesis during the division cycle without the contribution due to pole formation. As predicted by a model proposing that the surface growth of the cell is regulated by mass increase, we find a decrease in side wall synthesis in the latter half of the division cycle. This supports the proposal that, upon invagination, pole growth accommodates a significant proportion of the increasing cell mass and that residual side wall growth occurs in response to the residual mass increase not accommodated by pole volume. The observed side wall synthesis patterns support the proposal that mass increase is a major, and possibly sole, regulator of bacterial surface increase. Membrane synthesis during the division cycle of the gram-negative, rod-shaped bacteria Escherichia coli and Salmonella typhimurium has also been measured with similar methods. The rate of membrane synthesis--measured by incorporation of radioactive glycerol or palmitate relative to simultaneous labeling with radioactive leucine--exhibits the same pattern as peptidoglycan synthesis. The results are compatible with a model of cell surface growth containing the following elements. (i) During the period of the division cycle prior to invagination, growth of the cell occurs predominantly in the side wall and the cell grows only in length. (ii) When invagination begins, pole growth accommodates some cytoplasmic increase, leading to a concomitant decrease in side wall synthesis. (iii) Surface synthesis increases relative to mass synthesis during the last part of the division cycle because of pole formation. It is proposed here that membrane synthesis passively follows the pattern of peptidoglycan synthesis during the division cycle.
机译:一种用于确定分裂周期中肽聚糖合成模式的改进程序,使得可以在分裂周期中测量侧壁合成的速率,而不会由于极性的形成而产生影响。正如模型提出的那样,该模型建议细胞的表面生长受质量增加的调节,我们发现在分裂周期的后半段,侧壁合成的减少。这支持了这样的建议,即在发生内陷时,极点生长会适应增加的细胞质量的很大一部分,并且响应于极点体积无法容纳的剩余质量增加,会出现残余侧壁生长。观察到的侧壁合成模式支持以下建议:质量增加是细菌表面增加的主要且唯一的调节剂。革兰氏阴性,棒状细菌大肠杆菌和鼠伤寒沙门氏菌在分裂周期中的膜合成也已用类似方法进行了测量。膜的合成速率(通过掺入放射性甘油或棕榈酸酯相对于同时标记放射性亮氨酸来衡量)显示出与肽聚糖合成相同的模式。结果与包含以下元素的细胞表面生长模型兼容。 (i)在内陷之前的分裂周期期间,细胞的生长主要发生在侧壁中,并且细胞仅在长度上生长。 (ii)当开始内陷时,极点生长会适应一些细胞质的增加,从而导致侧壁合成的同时减少。 (iii)由于形成极点,在除法循环的最后部分,表面合成相对于质量合成增加。在此提出膜合成在分裂周期中被动地遵循肽聚糖合成的模式。

著录项

  • 作者

    Gally, D; Bray, K; Cooper, S;

  • 作者单位
  • 年度 1993
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  • 原文格式 PDF
  • 正文语种 en
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