Department of Microbiology, Cornell University, Ithaca, New York, USA.
mBio. 2023 Apr 25;14(2):e0047523. doi: 10.1128/mbio.00475-23. Epub 2023 Apr 5.
Proper synthesis and maintenance of a multilayered cell envelope are critical for bacterial fitness. However, whether mechanisms exist to coordinate synthesis of the membrane and peptidoglycan layers is unclear. In Bacillus subtilis, synthesis of peptidoglycan (PG) during cell elongation is mediated by an elongasome complex acting in concert with class A penicillin-binding proteins (aPBPs). We previously described mutant strains limited in their capacity for PG synthesis due to a loss of aPBPs and an inability to compensate by upregulation of elongasome function. Growth of these PG-limited cells can be restored by suppressor mutations predicted to decrease membrane synthesis. One suppressor mutation leads to an altered function repressor, FapR*, that functions as a super-repressor and leads to decreased transcription of fatty acid synthesis (FAS) genes. Consistent with fatty acid limitation mitigating cell wall synthesis defects, inhibition of FAS by cerulenin also restored growth of PG-limited cells. Moreover, cerulenin can counteract the inhibitory effect of β-lactams in some strains. These results imply that limiting PG synthesis results in impaired growth, in part, due to an imbalance of PG and cell membrane synthesis and that B. subtilis lacks a robust physiological mechanism to reduce membrane synthesis when PG synthesis is impaired. Understanding how a bacterium coordinates cell envelope synthesis is essential to fully appreciate how bacteria grow, divide, and resist cell envelope stresses, such as β-lactam antibiotics. Balanced synthesis of the peptidoglycan cell wall and the cell membrane is critical for cells to maintain shape and turgor pressure and to resist external cell envelope threats. Using Bacillus subtilis, we show that cells deficient in peptidoglycan synthesis can be rescued by compensatory mutations that decrease the synthesis of fatty acids. Further, we show that inhibiting fatty acid synthesis with cerulenin is sufficient to restore growth of cells deficient in peptidoglycan synthesis. Understanding the coordination of cell wall and membrane synthesis may provide insights relevant to antimicrobial treatment.
多层细胞包膜的适当合成和维持对细菌的适应性至关重要。然而,目前尚不清楚是否存在协调细胞膜和肽聚糖层合成的机制。在枯草芽孢杆菌中,在细胞伸长过程中,肽聚糖(PG)的合成是由一个伸长体复合物协同作用完成的,该复合物与 A 类青霉素结合蛋白(aPBPs)协同作用。我们之前描述了由于 aPBPs 的丧失和无法通过伸长体功能的上调来补偿,导致 PG 合成能力有限的突变菌株。这些 PG 受限细胞的生长可以通过预测降低膜合成的抑制突变来恢复。一个抑制突变导致改变功能的阻遏物 FapR*,它作为超阻遏物起作用,并导致脂肪酸合成(FAS)基因的转录减少。与脂肪酸限制减轻细胞壁合成缺陷一致, cerulenin 抑制 FAS 也恢复了 PG 受限细胞的生长。此外,cerulenin 可以抵消某些菌株中β-内酰胺的抑制作用。这些结果表明,限制 PG 合成会导致生长受损,部分原因是 PG 和细胞膜合成之间的不平衡,并且枯草芽孢杆菌缺乏在 PG 合成受损时减少膜合成的强大生理机制。了解细菌如何协调细胞包膜合成对于充分了解细菌如何生长、分裂以及抵抗细胞壁应激至关重要,例如β-内酰胺类抗生素。肽聚糖细胞壁和细胞膜的平衡合成对于维持细胞形状和膨压以及抵抗外部细胞壁威胁至关重要。使用枯草芽孢杆菌,我们表明缺乏肽聚糖合成的细胞可以通过降低脂肪酸合成的补偿性突变来挽救。此外,我们表明,用 cerulenin 抑制脂肪酸合成足以恢复缺乏肽聚糖合成的细胞的生长。了解细胞壁和膜合成的协调可能为抗菌治疗提供相关见解。