Resource sharing between central metabolism and cell envelope synthesis.

Ankita J Sachla, John D Helmann

Journal: Current opinion in microbiology 2021;60():34-43

PMID: 33581378

Abstract

Synthesis of the bacterial cell envelope requires a regulated partitioning of resources from central metabolism. Here, we consider the key metabolic junctions that provide the precursors needed to assemble the cell envelope. Peptidoglycan synthesis requires redirection of a glycolytic intermediate, fructose-6-phosphate, into aminosugar biosynthesis by the highly regulated branchpoint enzyme GlmS. MurA directs the downstream product, UDP-GlcNAc, specifically into peptidoglycan synthesis. Other shared resources required for cell envelope synthesis include the isoprenoid carrier lipid undecaprenyl phosphate and amino acids required for peptidoglycan cross-bridges. Assembly of the envelope requires a sharing of limited resources between competing cellular pathways and may additionally benefit from scavenging of metabolites released from neighboring cells or the formation of symbiotic relationships with a host.

Copyright © 2021 Elsevier Ltd. All rights reserved.

Address: Department of Microbiology, Cornell University, 370 Wing Hall, Wing Drive, Ithaca, NY 14853-8101, USA.; Department of Microbiology, Cornell University, 370 Wing Hall, Wing Drive, Ithaca, NY 14853-8101, USA. Electronic address: [email protected].
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