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Cloning of the subtilisin Pr1A gene from a strain of locust specific fungus, <Emphasis Type="Italic">Metarhizium anisopliae,</Emphasis> and functional expression of the protein in <Emphasis Type="Italic">Pichia pastoris</Emphasis>
Authors:Wei Zhang  Cao Yueqing  Xia Yuxian
Institution:(1) Genetic Engineering Research Center, College of Bioengineering, Chongqing University, Chongqing, 400030, People’s Republic of China;(2) Present address: Kerun Biopharmaceutical R&D Co. Ltd., Hilan Pharmaceutical Co. Ltd., Chongqing, 400041, People’s Republic of China;(3) Chongqing Engineering Research Center of Fungal Insecticides, Chongqing, 400030, People’s Republic of China
Abstract:The subtilisin-like protease Pr1A plays a role in insect cuticle breach and has been used in the development of advanced engineered biopesticides. We have identified and cloned the Pr1A gene from a locust specific Metarhizium anisopliae strain, CQMa102. The cDNA of Pr1A and its deduced protein sequence were deposited in GenBank (accession numbers EF627449 and ABR20899, respectively). Sequence analysis reveals that Pr1A belongs to the subtilisin-like serine protease family. Analysis of homologous species shows that the protein exhibits 99% identity with the subtilisin Pr1A from M. anisopliae var. acridum strain FI-985. The CQMa102 Pr1A protein was expressed in Pichia pastoris to verify its protease activity. Our results show that the Pr1A gene cloned from M. anisopliae strain CQMa102 has cuticle-degrading function and is a potential virulence factor for the development of engineered biopesticides.
Keywords:M  anisopliae            Subtilisin-like protease  Cuticle-degrading            P  pastoris
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