Abstract:Using high-property terminators enable significant enhancement of transcription termination, mRNA stability, heterologous gene expression in classic microorganisms. However, design of complex gene circuits was limited by the lack of terminators specifically adapted to Bacillus subtilis. [Objective] Exploiting new high-performance terminators from Bacillus subtilis and further redesigning to enrich the artificial terminators suitable for this chassis. [Methods] The terminators from Bacillus subtilis and Bacillus subtilis phage were respectively constructed into the terminator measurement plasmid to determine the termination efficiency (TE). Multiple tandem terminators were constructed with combinatorial patterns of strong-weak, strong-strong, and weak-weak and subsequently TEs of those tandem terminators were individually determined. The tandem terminators with high TE were harnessed to verify the function of heterologous expression of L-aspartate amino lyase (AspA) and β-glucuronidase (GusA) in B. subtilis. [Results] The TE of terminator TB5 is 98%, which is strongest among the natural terminators in B. subtilis. Meanwhile, expression level of GFP harboring TB5 was up-regulated by 2.2 folds, and the expression level of RFP was down-regulated by 27 folds. For the dual-tandem terminators, the expression levels of RFP regulated by TH1.5b-TB5 (TE=97%) and TB5-TB5 (TE=98%) tandem terminators were decreased by 30 folds. For the triple-tandem terminators, TB2-TB5-TB5 combination no longer increase the expression level of GFP compared with the corresponding dual combination. Nevertheless, the expression of RFP is only 1/300 of the control. Finally, heterologous expression of AspA and GusA confirmed that two tandem terminators, TH1.5b-TB5 and TB10-TB5, significantly improved the gene expression in B. subtilis. [Conclusion] Strong synthetic terminators are able to reinforce the heterologous gene expression in surrogate host. Importantly, the efficiency of termination is further improved by rational combination of natural terminators in tandem manner. These artificially redesigned terminators could be conveniently and portably constructed into bacterial gene circuits to augment and stabilize gene expression.