P62: A Cry3 expression system for the high-level protein expression in Bacillus subtilis

Monday, August 2, 2010
Pacific Concourse (Hyatt Regency San Francisco)
Soo-Keun Choi1, Su-Jin Lee1, Jae-Gu Pan1, Seung-Hwan Park1 and Eui-Joong Kim2, (1)Industrial Biotechnology & Bioenergy Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, South Korea, (2)Genofocus Inc., Daejeon, South Korea
Bacillus thuringiensis produces crystal proteins (Cry) that account for up to 25% of the dry cell weight during the stationary phase. The high-level expression and stationary phase-specific autoinduction of the cry gene led to development of a cry promoter-based Bacillus expression system. Among the various cry promoters, cry3Aa promoter was selected by comparing the lacZ expression levels in B. subtilis. An extracellular enzyme cellulase was highly upregulated during the stationary phase while under control of the cry3Aa promoter. Improvement of the cry3Aa promoter was obtained by modification of the promoter sequence. Specifically, a 5-fold increase in lacZ expression was obtained by changing both the -35 and -10 boxes of the cry3Aa promoter to the consensus sequence of the sA-dependent promoter of B. subtilis. The modified cry3Aa promoter produced a significantly higher yield of AprE, savinase and nattokinase, which suggests that the promoter may be useful for high-level protein expression in B. subtilis. [Supported by the 21C Frontier Microbial Genomics and Applications Center Program, MEST, and the Technology Development Program for Agriculture and Forestry, Ministry for Agriculture, Forestry and Fisheries, Republic of Korea]