Chain-length regulation by WzzE is necessary for, but genetically separable from, cyclic enterobacterial common antigen synthesis.

Bacteria of the order Enterobacterales (e.g., Escherichia, Klebsiella, Yersinia) produce an invariant glycan, enterobacterial common antigen (ECA), that plays a role in maintaining outer membrane (OM) impermeability. ECA is found as the headgroup of a phospholipid and attached to LPS in the OM, and as a periplasmic cyclic form (ECACYC). WzyE polymerizes ECA repeat units to form the ECA chain with final chain length regulated by WzzE, a class 1 polysaccharide co-polymerase (PCP1). PCP1 function studies have shown interaction of the PCP1 transmembrane helices with the polymerase and a secondary activity found in the periplasmic domain of the PCP1 are required for chain-length regulation. However, WzzE is also necessary for ECACYC biosynthesis, and it remains unclear why loss of WzzE prevents ECACYC production but not linear ECA production. Here, we constructed plasmid-based and chromosomal wzzE mutants in E. coli K-12 with alterations that affect chain-length regulation of other PCP1 and assessed their effects on ECACYC biogenesis. Our data show loss of chain-length regulation and ECACYC synthesis from mutations altering transmembrane helix 2 and mutations altering the periplasmic domain of WzzE. We also identified two WzzE variants to the same residue with identical, near wild type linear ECA chain-length regulation but differing effects on ECACYC production. Specifically, WzzEF104Y produces wild-type levels of ECACYC, while WzzEF104H produces twofold less ECACYC than wild type, demonstrating ECACYC synthesis is genetically separable from chain length regulation. Overall, our results show that chain-length regulation by WzzE is necessary but not sufficient for normal production of ECACYC.