A cell wall recycling shortcut that bypasses peptidoglycan de novo biosynthesis.

Abstract:

:We report a salvage pathway in Gram-negative bacteria that bypasses de novo biosynthesis of UDP N-acetylmuramic acid (UDP-MurNAc), the first committed peptidoglycan precursor, and thus provides a rationale for intrinsic fosfomycin resistance. The anomeric sugar kinase AmgK and the MurNAc α-1-phosphate uridylyl transferase MurU, defining this new cell wall sugar-recycling route in Pseudomonas putida, were characterized and engineered into Escherichia coli, channeling external MurNAc directly to peptidoglycan biosynthesis.

journal_name

Nat Chem Biol

journal_title

Nature chemical biology

authors

Gisin J,Schneider A,Nägele B,Borisova M,Mayer C

doi

10.1038/nchembio.1289

subject

Has Abstract

pub_date

2013-08-01 00:00:00

pages

491-3

issue

8

eissn

1552-4450

issn

1552-4469

pii

nchembio.1289

journal_volume

9

pub_type

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