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