N-terminal LysSN-His-tag improves the production of intracellular recombinant protein in Bacillus subtilis

Cell Biochem Funct. 2023 Oct;41(7):823-832. doi: 10.1002/cbf.3832. Epub 2023 Jul 29.

Abstract

Choosing fusion tags to enhance the recombinant protein levels in the cytoplasm of Bacillus subtilis has been limited. Our previous study demonstrated that His-tag at the N-terminus could increase the expression levels of the low-expression gene egfp, while significantly reducing the high-expression genes gfp+ and bgaB in the cytoplasm of B. subtilis. In this study, we aimed to prove the potential of a fusion tag, the combination of the N-terminal domain of B. subtilis lysyl tRNA synthetase (LysSN) and His-tag with varying numbers of histidine (6xHis, 8xHis, 10xHis) by investigating their effects on the expression levels of egfp, gfp+ and bgaB in B. subtilis. For the low-expression gene, LysSN-xHis-tag could enhance the fluorescent intensity of EGFP 23.5 times higher than EGFP without a fusion tag, and 1.5 times higher than that fused with only His-tag. For high-expression genes, the expression level of BgaB and GFP+ was 2.9 and 12.5 times higher than that of His-tag, respectively. The number of histidines in LysSN-xHis-tag did not influence the expression levels of the high-expression genes but affected the expression levels of the low-expression gene.

Keywords: Bacillus subtilis; LysSN; LysSN-His; N-terminal fusion; Pgrac promoter; Pgrac212 promoter; pHT vectors.

MeSH terms

  • Bacillus subtilis* / genetics
  • Bacillus subtilis* / metabolism
  • Gene Expression
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism

Substances

  • Recombinant Fusion Proteins
  • Recombinant Proteins