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ABSTRACT: Background
B. subtilis is an important organism in the biotechnological application. The efficient expression system is desirable in production of recombinant gene products in B. subtilis. Recently, we developed a new inducible expression system in B. subtilis, which directed by B. subtilis maltose utilization operon promoter Pglv. The system demonstrated high-level expression for target proteins in B. subtilis when induced by maltose. However, the system was markedly repressed by glucose. This limited the application of the system as a high-expression tool in biotechnology field. The aim of this study was to further improve the Pglv promoter system and enhance its expression strength.Results
Here, site-directed mutagenesis was facilitated to enhance the expression strength
SUBMITTER: Ming YM
PROVIDER: S-EPMC2908567 | biostudies-literature | 2010 Jul
REPOSITORIES: biostudies-literature