초록
<P><B>Background</B></P><P>Two overlapping genes <I>lacL</I> and <I>lacM</I> (<I>lacLM</I>) encoding for heterodimeric β-galactosidase from <I>Lactobacillus reuteri</I> were previously cloned and over-expressed in the food-grade host strain <I>Lactobacillus plantarum</I> WCFS1, using the inducible lactobacillal pSIP expression system. In this study, we analyzed different factors that affect the production of recombinant <I>L. reuteri</I> β-galactosidase.</P><P><B>Results</B></P><P>Various factors related to the cultivation, i.e. culture pH, growth temperature, glucose concentration, as well as the induction conditions, including cell concentration at induction point and inducer concentration, were tested. Under optimal fermentation conditions, the maximum β-galactosidase levels obtained were 130 U/mg protein and 35–40 U/ml of fermentation broth corresponding to the formation of approximately 200 mg of recombinant protein per litre of fermentation medium. As calculated from the specific activity of the purified enzyme (190 U/mg), β-galactosidase yield amounted to roughly 70% of the total soluble intracellular protein of the host organism. It was observed that pH and substrate (glucose) concentration are the most prominent factors affecting the production of recombinant β-galactosidase.</P><P><B>Conclusions</B></P><P>The over-expression of recombinant <I>L. reuteri</I> β-galactosidase in a food-grade host strain was optimized, which is of interest for applications of this enzyme in the food industry. The results provide more detailed insight into these lactobacillal expression systems and confirm the potential of the pSIP system for efficient, tightly controlled expression of enzymes and proteins in lactobacilli.</P>