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荧光 D-氨基酸揭示了双细胞细胞壁修饰对于噬菌蛭弧菌捕食的重要性。

Fluorescent D-amino-acids reveal bi-cellular cell wall modifications important for Bdellovibrio bacteriovorus predation.

机构信息

Molecular and Cellular Biochemistry Department, Indiana University Bloomington, Bloomington, IN, 47405, USA.

Department of Genetics, Harvard Medical School, Boston, MA, 02115, USA.

出版信息

Nat Microbiol. 2017 Dec;2(12):1648-1657. doi: 10.1038/s41564-017-0029-y. Epub 2017 Oct 3.

Abstract

Modification of essential bacterial peptidoglycan (PG)-containing cell walls can lead to antibiotic resistance; for example, β-lactam resistance by L,D-transpeptidase activities. Predatory Bdellovibrio bacteriovorus are naturally antibacterial and combat infections by traversing, modifying and finally destroying walls of Gram-negative prey bacteria, modifying their own PG as they grow inside prey. Historically, these multi-enzymatic processes on two similar PG walls have proved challenging to elucidate. Here, with a PG-labelling approach utilizing timed pulses of multiple fluorescent D-amino acids, we illuminate dynamic changes that predator and prey walls go through during the different phases of bacteria:bacteria invasion. We show formation of a reinforced circular port-hole in the prey wall, L,D-transpeptidase-mediated D-amino acid modifications strengthening prey PG during Bdellovibrio invasion, and a zonal mode of predator elongation. This process is followed by unconventional, multi-point and synchronous septation of the intracellular Bdellovibrio, accommodating odd- and even-numbered progeny formation by non-binary division.

摘要

细菌肽聚糖(PG)细胞壁的基本修饰可导致抗生素耐药性;例如,L,D-转肽酶活性导致β-内酰胺耐药性。捕食性蛭弧菌(Bdellovibrio bacteriovorus)具有天然的抗菌性,通过穿透、修饰并最终破坏革兰氏阴性猎物细菌的细胞壁来对抗感染,在猎物内部生长时会修饰自身的 PG。从历史上看,在两个类似的 PG 壁上进行这些多酶过程一直具有挑战性。在这里,我们利用多重荧光 D-氨基酸的时间脉冲 PG 标记方法,阐明了捕食者和猎物壁在细菌:细菌入侵的不同阶段所经历的动态变化。我们显示了在猎物壁上形成一个加固的圆形舷窗,L,D-转肽酶介导的 D-氨基酸修饰在 Bdellovibrio 入侵过程中增强了猎物 PG 的强度,以及捕食者的带状伸长模式。然后是细胞内 Bdellovibrio 的非常规、多点和同步的分隔,通过非二进制分裂适应奇数和偶数后代的形成。

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