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代谢塑造细胞。

Metabolism Shapes the Cell.

作者信息

Sperber Anthony M, Herman Jennifer K

机构信息

Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas, USA.

Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas, USA

出版信息

J Bacteriol. 2017 May 9;199(11). doi: 10.1128/JB.00039-17. Print 2017 Jun 1.

Abstract

More than 5 decades of work support the idea that cell envelope synthesis, including the inward growth of cell division, is tightly coordinated with DNA replication and protein synthesis through central metabolism. Remarkably, no unifying model exists to account for how these fundamentally disparate processes are functionally coupled. Recent studies demonstrate that proteins involved in carbohydrate and nitrogen metabolism can moonlight as direct regulators of cell division, coordinate cell division and DNA replication, and even suppress defects in DNA replication. In this minireview, we focus on studies illustrating the intimate link between metabolism and regulation of peptidoglycan (PG) synthesis during growth and division, and we identify the following three recurring themes. (i) Nutrient availability, not growth rate, is the primary determinant of cell size. (ii) The degree of gluconeogenic flux is likely to have a profound impact on the metabolites available for cell envelope synthesis, so growth medium selection is a critical consideration when designing and interpreting experiments related to morphogenesis. (iii) Perturbations in pathways relying on commonly shared and limiting metabolites, like undecaprenyl phosphate (Und-P), can lead to pleotropic phenotypes in unrelated pathways.

摘要

五十多年的研究工作支持了这样一种观点,即包括细胞分裂向内生长在内的细胞包膜合成,通过中心代谢与DNA复制和蛋白质合成紧密协调。值得注意的是,目前还没有一个统一的模型来解释这些根本不同的过程是如何在功能上耦合的。最近的研究表明,参与碳水化合物和氮代谢的蛋白质可以兼职作为细胞分裂的直接调节因子,协调细胞分裂和DNA复制,甚至抑制DNA复制中的缺陷。在这篇小型综述中,我们重点关注了一些研究,这些研究阐明了生长和分裂过程中代谢与肽聚糖(PG)合成调控之间的密切联系,并且我们确定了以下三个反复出现的主题。(i)营养物质的可用性而非生长速率,是细胞大小的主要决定因素。(ii)糖异生通量的程度可能对可用于细胞包膜合成的代谢物产生深远影响,因此在设计和解释与形态发生相关的实验时,生长培养基的选择是一个关键考虑因素。(iii)依赖于共同共享和有限的代谢物(如十一异戊烯磷酸(Und-P))的途径中的扰动,可能会导致不相关途径中出现多效性表型。

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