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Cel1, probably encoding a cellobiohydrolase lacking the substrate binding domain, is expressed in the initial infection phase of Claviceps purpurea on Secale cereale.

Abstract
At the host-pathogen interface of hyphae penetrating host cell walls in the rye ovary, a lack of cellulase-gold labeling of beta-1, 4-glucan in host cell walls indicates that enzymatic degradation of cellulose might be an important factor during the infection of rye by Claviceps purpurea. Using cbh1 from Trichoderma reesei as a probe, a putative cellulase gene (cel1) was isolated from a genomic library of the C. purpurea strain T5. The coding region of 1,616 bp contains two introns and a putative signal peptidase cleavage site, leaving a coding capacity of 437 amino acids for the mature protein. The derived amino acid sequence shares significant homology with other fungal cellobiohydrolases and lacks the substrate binding domain. Expression analysis using reverse transcriptase-polymerase chain reaction (RT-PCR) shows that cel1 is induced during the first days of infection of rye by C. purpurea. It may be involved in the penetration and degradation of host cell walls by depolymerizing plant beta-1, 4-glucan and, therefore, play a role in the infection process.
AuthorsU Müller, K B Tenberge, B Oeser, P Tudzynski
JournalMolecular plant-microbe interactions : MPMI (Mol Plant Microbe Interact) Vol. 10 Issue 2 Pg. 268-79 (Mar 1997) ISSN: 0894-0282 [Print] UNITED STATES
PMID9057332 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA Primers
  • DNA, Fungal
  • Glucans
  • 1,4-glucan
  • Cellulase
  • Cellulose 1,4-beta-Cellobiosidase
Topics
  • Amino Acid Sequence
  • Base Sequence
  • Cellulase (chemistry, genetics)
  • Cellulose 1,4-beta-Cellobiosidase
  • Claviceps (enzymology, genetics, pathogenicity)
  • Cloning, Molecular
  • DNA Primers (genetics)
  • DNA, Fungal (genetics)
  • Gene Expression
  • Genes, Fungal
  • Glucans (metabolism)
  • Microscopy, Immunoelectron
  • Molecular Sequence Data
  • Molecular Structure
  • Polymerase Chain Reaction
  • Restriction Mapping
  • Secale (metabolism, microbiology, ultrastructure)
  • Sequence Homology, Amino Acid
  • Virulence (genetics)

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