Cloning and sequence analysis of the endopolygalacturonase gene from the pitch canker fungus, Fusarium circinatum

Citation
Pm. Chimwamurombe et al., Cloning and sequence analysis of the endopolygalacturonase gene from the pitch canker fungus, Fusarium circinatum, CURR MICROB, 42(5), 2001, pp. 350-352
Citations number
12
Categorie Soggetti
Microbiology
Journal title
CURRENT MICROBIOLOGY
ISSN journal
03438651 → ACNP
Volume
42
Issue
5
Year of publication
2001
Pages
350 - 352
Database
ISI
SICI code
0343-8651(200105)42:5<350:CASAOT>2.0.ZU;2-P
Abstract
The fungus Fusarium circinatum causes pitch canker disease on mature pine t rees and root rot and damping-off of pine seedlings, Endopolygalacturonases (endoPGs) play a major role during penetration of plants by fungi. Digesti on of the pectic polysaccharides in the plant primary cell walls is one of the earliest functions of endoPGs during infection. The research objective was to clone and characterize the gene encoding endopolygalacturonase in F. circinatum. A 970-bp DNA fragment was cloned by using degenerate PCR ampli fication from F, circinatum DNA. Sequence data for this fragment were used to design specific primers for use in genome walking to amplify and sequenc e the remaining portion of the F. circinatum endoPG gene (Fcpg), The amino acid sequence predicted from this gene showed 90% and 87% similarity to Fus arium oxysporum and Fusarium moniliforme endoPGs, respectively.