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参与大肠杆菌细胞伸长必需过程的青霉素结合蛋白-1a或-1b的非必需性。

Dispensability of either penicillin-binding protein-1a or -1b involved in the essential process for cell elongation in Escherichia coli.

作者信息

Kato J, Suzuki H, Hirota Y

出版信息

Mol Gen Genet. 1985;200(2):272-7. doi: 10.1007/BF00425435.

DOI:10.1007/BF00425435
PMID:2993822
Abstract

A strain of Escherichia coli lacking the entire ponB gene and a strain lacking the proximal part of the ponA gene were constructed by substitution with a drug resistance gene. These strains lost either penicillin-binding protein(PBP)-1b or -1a totally and their growth was apparently normal at 30 degrees C and 42 degrees C except that growth of the ponB deletion strain was poor on a nutrient agar plate containing no NaCl at 30 degrees C as well as at 42 degrees C. Transductional experiments to introduce the ponB deletion into the ponA deletion strain, and vice versa, showed that the ponA ponB double deletion was lethal unless the deletion was functionally compensated, e.g., by the presence of a plasmid carrying either gene. Thus, either PBP-1b (ponB) or PBP-1a (ponA), but not both, is dispensable for cell viability, at least under ordinary culture conditions. Transductional experiments also suggested that the gamma component of PBP-1b or the PBP-1b lacking the C-terminal portion encoded in the distal region to the SphI site on the ponB was sufficient for supporting growth of the E. coli cell.

摘要

通过用耐药基因进行替换,构建了一株缺失整个ponB基因的大肠杆菌菌株和一株缺失ponA基因近端部分的菌株。这些菌株分别完全缺失青霉素结合蛋白(PBP)-1b或-1a,并且在30℃和42℃时它们的生长明显正常,只是ponB缺失菌株在30℃和42℃下于不含NaCl的营养琼脂平板上生长较差。将ponB缺失导入ponA缺失菌株以及反之的转导实验表明,除非缺失通过例如携带任一基因的质粒进行功能补偿,否则ponA ponB双缺失是致死的。因此,至少在普通培养条件下,PBP-1b(ponB)或PBP-1a(ponA)中的一种而非两者对于细胞活力是必需的。转导实验还表明,PBP-1b的γ组分或缺失ponB上SphI位点远端区域编码的C末端部分的PBP-1b足以支持大肠杆菌细胞的生长。

相似文献

1
Dispensability of either penicillin-binding protein-1a or -1b involved in the essential process for cell elongation in Escherichia coli.参与大肠杆菌细胞伸长必需过程的青霉素结合蛋白-1a或-1b的非必需性。
Mol Gen Genet. 1985;200(2):272-7. doi: 10.1007/BF00425435.
2
Overlapping of the coding regions for alpha and gamma components of penicillin-binding protein 1 b in Escherichia coli.大肠杆菌中青霉素结合蛋白1b的α和γ组分编码区的重叠
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The nucleotide sequences of the ponA and ponB genes encoding penicillin-binding protein 1A and 1B of Escherichia coli K12.编码大肠杆菌K12青霉素结合蛋白1A和1B的ponA和ponB基因的核苷酸序列。
Eur J Biochem. 1985 Mar 1;147(2):437-46. doi: 10.1111/j.1432-1033.1985.tb08768.x.
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Nucleotide sequence of the pbpA gene and characteristics of the deduced amino acid sequence of penicillin-binding protein 2 of Escherichia coli K12.大肠杆菌K12的pbpA基因核苷酸序列及青霉素结合蛋白2推导氨基酸序列的特征
Eur J Biochem. 1986 Oct 15;160(2):231-8. doi: 10.1111/j.1432-1033.1986.tb09961.x.

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Proc Natl Acad Sci U S A. 1960 Jan;46(1):57-64. doi: 10.1073/pnas.46.1.57.
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A gene coding for a periplasmic protein is located near the locus for termination of chromosome replication in Escherichia coli.编码一种周质蛋白的基因位于大肠杆菌染色体复制终止位点附近。
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Molecular divergence of a major peptidoglycan synthetase with transglycosylase-transpeptidase activities in Escherichia coli --- penicillin-binding protein 1Bs.
低肽聚糖合成能力会削弱 在高盐浓度下的生长。
mBio. 2024 Apr 10;15(4):e0032524. doi: 10.1128/mbio.00325-24. Epub 2024 Mar 1.
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Comparative genomics hints at dispensability of multiple essential genes in two Escherichia coli L-form strains.比较基因组学提示在两种大肠杆菌 L 型菌株中有多个必需基因的非必需性。
Biosci Rep. 2023 Oct 31;43(10). doi: 10.1042/BSR20231227.
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The Bacterial Cell Wall: From Lipid II Flipping to Polymerization.细菌细胞壁:从脂质 II 翻转到聚合。
Chem Rev. 2022 May 11;122(9):8884-8910. doi: 10.1021/acs.chemrev.1c00773. Epub 2022 Mar 11.
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The LpoA activator is required to stimulate the peptidoglycan polymerase activity of its cognate cell wall synthase PBP1a.LpoA激活剂是刺激其同源细胞壁合成酶PBP1a的肽聚糖聚合酶活性所必需的。
Proc Natl Acad Sci U S A. 2021 Aug 31;118(35). doi: 10.1073/pnas.2108894118.
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MltG activity antagonizes cell wall synthesis by both types of peptidoglycan polymerases in Escherichia coli.MltG 活性通过两种类型的肽聚糖聚合酶拮抗大肠埃希菌的细胞壁合成。
Mol Microbiol. 2021 Jun;115(6):1170-1180. doi: 10.1111/mmi.14660. Epub 2020 Dec 19.
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A conserved subcomplex within the bacterial cytokinetic ring activates cell wall synthesis by the FtsW-FtsI synthase.细菌细胞分裂环内的一个保守亚基复合物通过 FtsW-FtsI 合成酶激活细胞壁合成。
Proc Natl Acad Sci U S A. 2020 Sep 22;117(38):23879-23885. doi: 10.1073/pnas.2004598117. Epub 2020 Sep 9.
9
Simultaneously inhibiting undecaprenyl phosphate production and peptidoglycan synthases promotes rapid lysis in Escherichia coli.同时抑制十一烯基磷酸的产生和肽聚糖合成酶可促进大肠杆菌的快速裂解。
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Mechanical Genomic Studies Reveal the Role of d-Alanine Metabolism in Pseudomonas aeruginosa Cell Stiffness.机械基因组学研究揭示了 D-丙氨酸代谢在铜绿假单胞菌细胞刚性中的作用。
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大肠杆菌中具有转糖基酶-转肽酶活性的主要肽聚糖合成酶——青霉素结合蛋白1Bs的分子差异
Biochem Biophys Res Commun. 1982 Apr 29;105(4):1546-53. doi: 10.1016/0006-291x(82)90964-0.
4
Synthetic ColE1 Plasmids carrying genes for penicillin-binding proteins in Escherichia coli.携带大肠杆菌青霉素结合蛋白基因的合成ColE1质粒。
Plasmid. 1981 Jul;6(1):86-98. doi: 10.1016/0147-619x(81)90056-1.
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Dual enzyme activities of cell wall peptidoglycan synthesis, peptidoglycan transglycosylase and penicillin-sensitive transpeptidase, in purified preparations of Escherichia coli penicillin-binding protein 1A.在大肠杆菌青霉素结合蛋白1A的纯化制剂中,细胞壁肽聚糖合成的两种酶活性,即肽聚糖转糖基酶和青霉素敏感转肽酶。
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6
On the process of cellular division in Escherichia coli: isolation and characterization of penicillin-binding proteins 1a, 1b, and 3.关于大肠杆菌细胞分裂过程:青霉素结合蛋白1a、1b和3的分离与特性分析
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4499-503. doi: 10.1073/pnas.77.8.4499.
7
In vitro peptidoglycan polymerization catalysed by penicillin binding protein 1b of Escherichia coli K-12.由大肠杆菌K-12的青霉素结合蛋白1b催化的体外肽聚糖聚合反应。
FEBS Lett. 1980 Feb 11;110(2):245-9. doi: 10.1016/0014-5793(80)80083-4.
8
An essential gene for replication of the mini-F plasmid from origin I.来自I型原点的微小F质粒复制所需的一个必需基因。
Mol Gen Genet. 1984;196(1):59-63. doi: 10.1007/BF00334092.
9
A novel glycan polymerase that synthesizes uncross-linked peptidoglycan in Escherichia coli.一种在大肠杆菌中合成非交联肽聚糖的新型聚糖聚合酶。
FEBS Lett. 1984 Mar 12;168(1):155-60. doi: 10.1016/0014-5793(84)80226-4.
10
Penicillin-binding proteins and the future of beta-lactam antibiotics. The Seventh Fleming Lecture.青霉素结合蛋白与β-内酰胺类抗生素的未来。第七届弗莱明讲座。
J Gen Microbiol. 1983 May;129(5):1247-60. doi: 10.1099/00221287-129-5-1247.