THE SUCCINYL AND ACETYL MODIFICATIONS OF SUCCINOGLYCAN INFLUENCE SUSCEPTIBILITY OF SUCCINOGLYCAN TO CLEAVAGE BY THE RHIZOBIUM-MELILOTI GLYCANASES EXOK AND EXSH

Authors
Citation
Gm. York et Gc. Walker, THE SUCCINYL AND ACETYL MODIFICATIONS OF SUCCINOGLYCAN INFLUENCE SUSCEPTIBILITY OF SUCCINOGLYCAN TO CLEAVAGE BY THE RHIZOBIUM-MELILOTI GLYCANASES EXOK AND EXSH, Journal of bacteriology, 180(16), 1998, pp. 4184-4191
Citations number
46
Categorie Soggetti
Microbiology
Journal title
ISSN journal
00219193
Volume
180
Issue
16
Year of publication
1998
Pages
4184 - 4191
Database
ISI
SICI code
0021-9193(1998)180:16<4184:TSAAMO>2.0.ZU;2-J
Abstract
In Rhizobium meliloti (Sinorhizobium meliloti) cultures, the endo-1,3- 1,4-beta-glycanases ExoK and ExsH depolymerize nascent high-molecular- weight (HMW) succinoglycan to yield low-molecular-weight (LMW) succino glycan. We report here that the succinyl and acetyl modifications of s uccinoglycan influence the susceptibility of succinoglycan to cleavage by these glycanases. It was previously shown that exoH mutants, which are blocked in the succinylation of succinoglycan, exhibit a defect i n the production of LMW succinoglycan. We have determined that exoZ mu tants, which are blocked in the acetylation of succinoglycan, exhibit an increase in production of LMW succinoglycan. For both wild-type and exoZ mutant strains, production of LMW succinoglycan is dependent on the exoK(+) and exsH(+) genes, implying that the ExoK and ExsH glycana ses cleave HMW succinoglycan to yield LMW succinoglycan. By supplement ing cultures of glycanase-deficient strains with exogenously added Exo K or ExsH, we have demonstrated directly that the absence of the acety l group increases the susceptibility of succinoglycan to cleavage by E xoK and ExsH, that the absence of the succinyl group decreases the sus ceptibility of succinoglycan to cleavage, and that the succinyl effect outweighs the acetyl effect for succinoglycan lacking both modificati ons. Strikingly, nonsuccinylated succinoglycan actually can be cleaved by ExoK and ExsH to yield LMW succinoglycan, but only when the glycan ases are added to cultures at greater than physiologically relevant co ncentrations. Thus, we conclude that the molecular weight distribution of succinoglycan in R. meliloti cultures is determined by both the le vels of ExoK and ExsH glycanase expression and the susceptibility of s uccinoglycan to cleavage.