几丁质、几丁质寡糖和几丁质双糖在大肠杆菌中的代谢:ChiA、ChbR、ChbF和ChbG的作用重新分配

IF 0.1 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Microbial Physiology Pub Date : 2021-01-01 Epub Date: 2021-04-01 DOI:10.1159/000515178
Axel Walter, Simon Friz, Christoph Mayer
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引用次数: 6

摘要

大肠杆菌不能在聚合和寡聚几丁质上生长,但可以在几丁质二糖(GlcNAc-GlcNAc;N,N'-二乙酰壳聚糖)和几丁质三糖(GlcNAc-GlcNAc-GlcNAc;N,N',N' -三乙酰壳三糖)通过chb操纵子(chbBCARFG)的表达。磷酸转移酶系统(PTS)转运体ChbBCA促进了这两种糖在细胞膜上的转运以及它们在非还原端伴随的磷酸化,分别在细胞内产生GlcNAc6 -磷酸-GlcNAc (GlcNAc6P-GlcNAc)和GlcNAc6P-GlcNAc-GlcNAc。我们重新研究了PTS产物的细胞内分解代谢,从而纠正了报道的6-磷酸糖苷酶ChbF、单去乙酰化酶ChbG和转录调节因子ChbR的功能。chbF突变体中葡萄糖胺6P-GlcNAc (GlcN6P-GlcNAc)和GlcN6P-GlcNAc- glcnac的细胞内积累揭示了ChbG作为一种单去乙酰化酶的作用,该酶可以去除非还原端n-乙酰基。因此,GlcN6P-而非glcnac6p -糖可能作为ChbR的共激活剂。此外,ChbF将GlcN6P从前两种糖的非还原端去除,从而降解chb操纵子的诱导剂,促进糖上的生长。因此,ChbF不能水解非还原端glcnac6p残基,这与之前的假设相反,但与结构建模数据和ChbF所属的糖苷酶4家族的不同寻常的催化机制一致。我们也驳斥了ChiA是一种双功能的内源性几丁质酶/溶菌酶ChiA的假设,并表明它不能降解肽聚糖,但在体外和体内都是一种真正的几丁质酶,当异位表达时,大肠杆菌可以在几丁质寡糖上生长。总的来说,本研究修订了我们对大肠杆菌几丁质、几丁质低聚糖和几丁质双糖代谢的认识。
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Chitin, Chitin Oligosaccharide, and Chitin Disaccharide Metabolism of Escherichia coli Revisited: Reassignment of the Roles of ChiA, ChbR, ChbF, and ChbG.

Escherichia coli is unable to grow on polymeric and oligomeric chitin, but grows on chitin disaccharide (GlcNAc-GlcNAc; N,N'-diacetylchitobiose) and chitin trisaccharide (GlcNAc-GlcNAc-GlcNAc; N,N',N''-triacetylchitotriose) via expression of the chb operon (chbBCARFG). The phosphotransferase system (PTS) transporter ChbBCA facilitates transport of both saccharides across the inner membrane and their concomitant phosphorylation at the non-reducing end, intracellularly yielding GlcNAc 6-phosphate-GlcNAc (GlcNAc6P-GlcNAc) and GlcNAc6P-GlcNAc-GlcNAc, respectively. We revisited the intracellular catabolism of the PTS products, thereby correcting the reported functions of the 6-phospho-glycosidase ChbF, the monodeacetylase ChbG, and the transcriptional regulator ChbR. Intracellular accumulation of glucosamine 6P-GlcNAc (GlcN6P-GlcNAc) and GlcN6P-GlcNAc-GlcNAc in a chbF mutant unraveled a role for ChbG as a monodeacetylase that removes the N-acetyl group at the non-reducing end. Consequently, GlcN6P- but not GlcNAc6P-containing saccharides likely function as coactivators of ChbR. Furthermore, ChbF removed the GlcN6P from the non-reducing terminus of the former saccharides, thereby degrading the inducers of the chb operon and facilitating growth on the saccharides. Consequently, ChbF was unable to hydrolyze GlcNAc6P-residues from the non-reducing end, contrary to previous assumptions but in agreement with structural modeling data and with the unusual catalytic mechanism of the family 4 of glycosidases, to which ChbF belongs. We also refuted the assumption that ChiA is a bifunctional endochitinase/lysozyme ChiA, and show that it is unable to degrade peptidoglycans but acts as a bona fide chitinase in vitro and in vivo, enabling growth of E. coli on chitin oligosaccharides when ectopically expressed. Overall, this study revises our understanding of the chitin, chitin oligosaccharide, and chitin disaccharide metabolism of E. coli.

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