Stevens M P, Hänfling P, Jann B, Jann K, Roberts I S
Department of Microbiology and Immunology, University of Leicester, UK.
FEMS Microbiol Lett. 1994 Nov 15;124(1):93-8. doi: 10.1111/j.1574-6968.1994.tb07267.x.
Expression of the Escherichia coli K5 antigen was used as a model system to study the role of known regulators of gene expression on production of group II capsules in E. coli. Only mutations in the rfaH gene had an effect on production of the K5 antigen, abolishing the expression of any detectable capsule at 37 degrees C. None of the mutations studied induced capsule expression at 18 degrees C. A sequence, termed JUMPstart, found in group II capsule gene clusters and upstream of a number of polysaccharide biosynthesis genes in enteric bacteria is homologous to sequences found in RfaH regulated operons. This may indicate a common mode of regulation of these polysaccharide biosynthesis genes by RfaH.
大肠杆菌K5抗原的表达被用作一个模型系统,以研究已知基因表达调控因子对大肠杆菌中II型荚膜产生的作用。只有rfaH基因突变对K5抗原的产生有影响,在37℃时消除了任何可检测到的荚膜表达。所研究的突变均未在18℃时诱导荚膜表达。在II型荚膜基因簇以及肠道细菌中许多多糖生物合成基因上游发现的一个名为JUMPstart的序列,与RfaH调控的操纵子中发现的序列同源。这可能表明RfaH对这些多糖生物合成基因有共同的调控模式。