Molecular Cloning, Characterization, and Expression of a Chitinase from the Entomopathogenic Fungus Paecilomyces javanicus
Author(s) -
ChienCheng Chen,
H.G. Ashok Kumar,
Senthil Kumar,
S. S. Tzean,
KaiWun Yeh
Publication year - 2007
Publication title -
current microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.578
H-Index - 90
eISSN - 1432-0991
pISSN - 0343-8651
DOI - 10.1007/s00284-006-0405-y
Subject(s) - biology , chitinase , paecilomyces , complementary dna , entomopathogenic fungus , open reading frame , molecular cloning , rhizoctonia solani , microbiology and biotechnology , rapid amplification of cdna ends , aspergillus nidulans , heterologous expression , peptide sequence , gene , biochemistry , botany , beauveria bassiana , biological pest control , mutant , recombinant dna
Paecilomyces javanicus is an entomopathogenic fungus of coleopteran and lepidopteran insects. Here we report on cloning, characterization, and expression patterns of a chitinase from P. javanicus. A strong chitinase activity was detected in P. javanicus cultures added to chitin. The full-length cDNA, designated PjChi-1, was cloned from mycelia by using both degenerate primer/reverse transcription polymerase chain reaction (RT-PCR) amplification and 5'-/3'-RACE extension. The 1.18-kb cDNA gene contains a 1035-bp open reading frame and encodes a 345-amino acid polypeptide with a deduced molecular mass of 37 kDa. A conserved motif for chitinase activity -F82DGIDIDWE90- was present in deduced amino acid sequence. Both RT-PCR and Northern analysis revealed that the expression of the PjChi gene was constitutive at low level, but enhanced to high level when chitin was the substrate. Fungal inhibitory assay showed that PjChi-1 inhibited the growth of phytopathogenic fungi such as Sclerotium rolfsii, Colletotrichum gloeosporioides, Aspergillus nidulans, and Rhizoctonia solani.
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