Staphylococcus aureus as an emerging model to study bacterial cell division.

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Félix Ramos-León, Kumaran S Ramamurthi
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引用次数: 0

Abstract

Research on bacterial cell division has traditionally focused on rod-shaped model organisms such as Escherichia coli and Bacillus subtilis. While these models have been important in uncovering broadly conserved factors involved in bacterial cell division, the assortment of bacterial shapes, cell wall structures, and lifestyles highlights the need to broaden the scope of study. This includes not only understanding how conserved mechanisms are adapted to diverse cellular morphologies but also discovering mechanisms that arise as specific adaptations to unique cellular shapes. In this context, alternative models such as Staphylococcus aureus are emerging to provide insight into how Gram-positive cocci overcome the challenge of lacking obvious cellular polarity to ensure accurate placement of the division septum and undergo binary fission. In this review, we highlight recent research that reveals how S. aureus performs several distinct but interrelated processes, including peptidoglycan assembly, placement of the cell division septum, and how the division septum can be used as a hub for modifying the peptidoglycan to decorate the cell surface of S. aureus.

金黄色葡萄球菌作为研究细菌细胞分裂的新兴模型。
传统上,对细菌细胞分裂的研究主要集中在杆状模式生物上,如大肠杆菌和枯草芽孢杆菌。虽然这些模型在揭示细菌细胞分裂中涉及的广泛保守因素方面很重要,但细菌形状、细胞壁结构和生活方式的分类突出了扩大研究范围的必要性。这不仅包括了解保守机制如何适应不同的细胞形态,还包括发现作为对独特细胞形状的特定适应而出现的机制。在这种情况下,金黄色葡萄球菌等替代模型正在出现,以深入了解革兰氏阳性球菌如何克服缺乏明显细胞极性的挑战,以确保分裂隔膜的准确位置并进行二元裂变。在这篇综述中,我们重点介绍了最近的研究,揭示了金黄色葡萄球菌如何执行几个不同但相互关联的过程,包括肽聚糖组装,细胞分裂间隔的放置,以及分裂间隔如何作为修饰肽聚糖的枢纽来修饰金黄色葡萄球菌的细胞表面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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