Cloning, sequencing, and expression of the rpoD gene encoding the primary sigma factor of Xanthomonas campestris

Biochem Biophys Res Commun. 1997 Mar 27;232(3):712-8. doi: 10.1006/bbrc.1997.6272.

Abstract

A DNA fragment encoding the primary sigma factor from Xanthomonas campestris pv. campestris was cloned and sequenced. The gene (rpoD) encodes a polypeptide of 622 amino acids with a calculated MW of 70,700. The deduced amino acid sequence exhibits extensive sequence homology to the conserved regions of the primary sigma factors from bacteria. The gene product expressed in Escherichia coli, detected by Western blot analysis, had a MW similar to that estimated for the purified protein in SDS-PAGE. The NH2-terminal amino acid sequence determined chemically matched with that deduced from the nucleotide sequence of the rpoD gene. The calculated pI value (9.31) for the X. campestris primary sigma factor is much higher than the values observed for the analogous proteins from other bacteria.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacterial Proteins / genetics*
  • Base Sequence
  • Cloning, Molecular
  • DNA Primers / genetics
  • DNA, Bacterial / genetics
  • DNA-Directed RNA Polymerases / genetics*
  • Escherichia coli / genetics
  • Gene Expression
  • Genes, Bacterial*
  • Molecular Sequence Data
  • Open Reading Frames
  • Pseudomonas aeruginosa / genetics
  • Restriction Mapping
  • Sequence Homology, Amino Acid
  • Sigma Factor / genetics*
  • Species Specificity
  • Xanthomonas campestris / genetics*

Substances

  • Bacterial Proteins
  • DNA Primers
  • DNA, Bacterial
  • Sigma Factor
  • RNA polymerase sigma 70
  • DNA-Directed RNA Polymerases

Associated data

  • GENBANK/U82763