Increase Of A Fibrinolytic Enzyme Production Through Promoter Replacement Of Apre3-5 From Bacillus Subtilis Ch3-5

Bacillus subtilis CH3-5 isolated from cheonggukjang secretes a 28 kDa protease with a strong fibrinolytic activity. Its gene, aprE3-5, was cloned and expressed in a heterologous host (Jeong et al., 2007). In this study, the promoter of aprE3-5 was replaced with other stronger promoters (Pcry3A, P10, PSG1, PsrfA) of Bacillus spp. using PCR. The constructed chimeric genes were cloned into pHY300PLK vector, and then introduced into B. subtilis WB600. The P10 promoter conferred the highest fibrinolytic activity, i.e., 1.7-fold higher than that conferred by the original promoter. Overproduction of the 28 kDa protease was confirmed using SDS-PAGE and fibrin zymography. RTqPCR analysis showed that aprE3-5 expression was 2.0-fold higher with the P10 promoter than with the original promoter. Change of the initiation codon from GTG to ATG further increased the fibrinolytic activity. The highest aprE3-5 expression was observed when two copies of the P10 promoter were placed in tandem upstream of the ATG initiation codon. The construct with P10 promoter and ATG and the construct with two copies of P10 promoter in tandem and ATG exhibited 117% and 148% higher fibrinolytic activity, respectively, than that exhibited by the construct containing P10 promoter and GTG. These results confirmed that significant overproduction of a fibrinolytic enzyme can be achieved by suitable promoter modification, and this approach may have applications in the industrial production of AprE3-5 and related fibrinolytic enzymes. Keywords: Bacillus subtilis, promoter replacement, gene expression, fibrinolytic enzymesFibrinolytic enzymes secreted by some Bacillus spp. have been the subject of many researches owing to their application as potential anti-thrombotic agents [1, 2]. Nattokinase is the most well-known enzyme, and commercially sold as a neutraceutical supplement. The overproduction of fibrinolytic enzymes, such as nattokinase, is important for the development of various products that contain them. To achieve this goal, various methods have been tried including screening of novel strains with strong fibrinolytic activities [3-5], optimizing