Unknown

Dataset Information

0

A family of serine proteases of Clavibacter michiganensis subsp. michiganensis: chpC plays a role in colonization of the host plant tomato.


ABSTRACT: Genes for seven putative serine proteases (ChpA-ChpG) belonging to the trypsin subfamily and homologous to the virulence factor pat-1 were identified on the chromosome of Clavibacter michiganensis subsp. michiganensis (Cmm) NCPPB382. All proteases have signal peptides indicating export of these proteins. Their putative function is suggested by two motifs and an aspartate residue typical for serine proteases. Furthermore, six cysteine residues are located at conserved positions. The genes are clustered in a chromosomal region of about 50 kb with a significantly lower G + C content than common for Cmm. The genes chpA, chpB and chpD are pseudogenes as they contain frame shifts and/or in-frame stop codons. The genes chpC and chpG were inactivated by the insertion of an antibiotic resistance cassette. The chpG mutant was not impaired in virulence. However, in planta the titre of the chpC mutant was drastically reduced and only weak disease symptoms were observed. Complementation of the chpC mutant by the wild-type allele restored full virulence. ChpC is the first chromosomal gene of Cmm identified so far that affects the interaction of the pathogen with the host plant.

SUBMITTER: Stork I 

PROVIDER: S-EPMC6640399 | biostudies-literature | 2008 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

A family of serine proteases of Clavibacter michiganensis subsp. michiganensis: chpC plays a role in colonization of the host plant tomato.

Stork Ines I   Gartemann Karl-Heinz KH   Burger Annette A   Eichenlaub Rudolf R  

Molecular plant pathology 20080901 5


Genes for seven putative serine proteases (ChpA-ChpG) belonging to the trypsin subfamily and homologous to the virulence factor pat-1 were identified on the chromosome of Clavibacter michiganensis subsp. michiganensis (Cmm) NCPPB382. All proteases have signal peptides indicating export of these proteins. Their putative function is suggested by two motifs and an aspartate residue typical for serine proteases. Furthermore, six cysteine residues are located at conserved positions. The genes are clu  ...[more]

Similar Datasets

| S-EPMC3811524 | biostudies-literature
2021-08-10 | GSE160971 | GEO
| S-EPMC3754172 | biostudies-literature
| S-EPMC5933903 | biostudies-literature
| S-EPMC4609890 | biostudies-literature
| S-EPMC6881797 | biostudies-literature
| S-EPMC6946519 | biostudies-literature
| S-EPMC2258877 | biostudies-literature
| S-EPMC5478997 | biostudies-literature
| S-EPMC8524973 | biostudies-literature