摘要
为提高枯草芽孢杆菌168(Bacillus subtilis 168)细菌素subtilosin A的产量使其能够应用到食品防腐、医药卫生等行业。采用重叠延伸PCR将强启动子P43分别和subtilosin A合成酶基因簇中关键酶基因sbo-albA、albB-albC连接到一起,构建了高表达载体。采用改进的电击法将重组载体转化到Bacillus subtilis 168中,通过高效液相色谱(HPLC)检测,确定subtilosin A产量得到了提高,进一步通过抑菌实验证明其抑菌活性也获得了提高。该方法为提高subtilosin A产量,进而应用到生产实践中提供了理论参考。
For improving Bacillus subtilis 168 bacteriocin subtilosin A production and applying to food preservation, medical science and so on,P43was linked to key enzyme gene sbo-albA,albB-albC of subtilosin A operon using SOE-PCR:High expressing vector was constructed.This recombinant vector was transformed into Bacillus subtilis 168 by high osmolarity electroporation method.HPLC assay showed subtilosin A production was improved.Inhibited method also showed the improving.This method will provide theory reference of improving subtilosin A production and applying in productive practice.
出处
《食品工业科技》
CAS
CSCD
北大核心
2013年第23期164-167,171,共5页
Science and Technology of Food Industry
基金
国家自然科学基金(31271936)
河北省自然科学基金资助项目(C2007000191)
徐州市科技计划项目(XF11C056)
徐州工程学院科研项目(SPY2010209)