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细胞包膜合成在包膜生长和细胞质密度方面的作用 。 你提供的原文似乎不完整,句末的“in.”后面应该还有内容。

The role of cell-envelope synthesis for envelope growth and cytoplasmic density in .

作者信息

Kitahara Yuki, Oldewurtel Enno R, Wilson Sean, Sun Yingjie, Altabe Silvia, de Mendoza Diego, Garner Ethan C, van Teeffelen Sven

机构信息

Département de Microbiologie, Infectiologie, et Immunologie, Faculté de Médecine, Université de Montréal, Montréal, QC, Canada.

Université de Paris, Paris, France.

出版信息

PNAS Nexus. 2022 Jul 26;1(4):pgac134. doi: 10.1093/pnasnexus/pgac134. eCollection 2022 Sep.

Abstract

All cells must increase their volumes in response to biomass growth to maintain intracellular mass density within physiologically permissive bounds. Here, we investigate the regulation of volume growth in the Gram-positive bacterium . To increase volume, bacteria enzymatically expand their cell envelopes and insert new envelope material. First, we demonstrate that cell-volume growth is determined indirectly, by expanding their envelopes in proportion to mass growth, similarly to the Gram-negative , despite their fundamentally different envelope structures. Next, we studied, which pathways might be responsible for robust surface-to-mass coupling: We found that both peptidoglycan synthesis and membrane synthesis are required for proper surface-to-mass coupling. However, surprisingly, neither pathway is solely rate-limiting, contrary to wide-spread belief, since envelope growth continues at a reduced rate upon complete inhibition of either process. To arrest cell-envelope growth completely, the simultaneous inhibition of both envelope-synthesis processes is required. Thus, we suggest that multiple envelope-synthesis pathways collectively confer an important aspect of volume regulation, the coordination between surface growth, and biomass growth.

摘要

为了将细胞内质量密度维持在生理允许范围内,所有细胞必须随着生物量的增长而增加其体积。在此,我们研究革兰氏阳性细菌中体积增长的调控机制。为了增加体积,细菌通过酶促作用扩展其细胞壁并插入新的细胞壁物质。首先,我们证明细胞体积的增长是间接决定的,即通过与其质量增长成比例地扩展其细胞壁来实现,这与革兰氏阴性菌类似,尽管它们的细胞壁结构存在根本差异。接下来,我们研究了哪些途径可能负责稳健的表面积与质量耦合:我们发现肽聚糖合成和膜合成对于正确的表面积与质量耦合都是必需的。然而,令人惊讶的是,与广泛的观点相反,这两个途径都不是唯一的限速因素,因为在完全抑制任何一个过程后,细胞壁的生长仍以降低的速率继续。为了完全阻止细胞壁的生长,需要同时抑制这两个细胞壁合成过程。因此,我们认为多个细胞壁合成途径共同赋予了体积调节的一个重要方面,即表面生长和生物量生长之间的协调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/213d/9802158/5c0eb105bdbe/pgac134fig1.jpg

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