Cloning and overexpression of Pochonia chlamydosporia chitinase gene pcchi44, a potential virulence factor in infection against nematodes

• Published in: Process biochemistry (1991) 2010-05, Vol.45 (5), p.810-814
• Main Authors: Mi, Qili, Yang, Jinkui, Ye, Fengping, Gan, Zhongwei, Wu, Changwei, Niu, Xuemei, Zou, Chenggang, Zhang, Ke-Qin
• Format: Article
• Language: English
• Subjects: Bombyx mori; Chitinase; Escherichia coli; Expression; Gene cloning; Km value; Meloidogyne incognita; Nematoda; Phylogenetic analysis; Pochonia chlamydosporia
• ISSN: 1359-5113; 1873-3298
• DOI: 10.1016/j.procbio.2010.01.022

The fungus Pochonia chlamydosporia is a biocontrol agent with commercial potential for root-knot and cyst nematodes. In this study, a gene (designated pcchi44) encoding an extracellular endochitinase was isolated for the first time from P. chlamydosporia using degenerate primers and a genome walking technique. The 2385-bp pcchi44 sequence is interrupted by three introns and encodes a 424-amino acid polypeptide. The cDNA sequence of pcchi44 was amplified via reverse transcription polymerase chain reaction and overexpressed in Escherichia coli BL21. The recombinant chitinase PCCHI44 was purified as a protein of ca. 44 kDa with an optimal activity at pH 6.0 and 50 °C. The V max and K m value of PCCHI44 using 4-methylumbelliferyl-β- d- N, N′, N″-triacetylchitotrioside as substrate were 8.37 × 10 −3 μM s −1 and 9.65 μM, respectively. The hydrolytic activity of PCCHI44 could be completely inhibited by acetazolamide. The chitinase PCCHI44 could damage eggs of both the root-knot nematode Meloidogyne incognita and the insect Bombyx mori.