Engineering of Bacillus Promoters Based on Interacting Motifs between UP Elements and RNA Polymerase (RNAP) α-Subunit

• Published in: International journal of molecular sciences Vol. 23; no. 21; p. 13480
• Main Authors: Li, Youran, Ma, Xufan, Zhang, Liang, Ding, Zhongyang, Xu, Sha, Gu, Zhenghua, Shi, Guiyang
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.11.2022; MDPI
• Subjects: Bacillus; Bacillus licheniformis; Binding; Cell culture; Cell growth; DNA-directed RNA polymerase; E coli; Engineering; Fluorescence polarization; Gene expression; In vivo methods and tests; Kinases; promoter engineering; Promoters; Proteins; RNA polymerase; Signal transduction; UP element; α-CTD
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms232113480

Bacillus genetics need more versatile promoters for gene circuit engineering. UP elements are widely distributed in noncoding regions and interact with the α-subunit of RNA polymerase (RNAP). They can be applied as a standard element for synthetic biology. Characterization of the binding motif between UP elements and RNAP may assist with rational and effective engineering. In this study, 11 Bacillus constitutive promoters were screened for strength in Bacillus licheniformis. The motif in UP elements from a strong native promoter, PLan, was characterized. The influence of specific sequences on RNAP binding and expression strength was investigated both in vitro and in vivo. It was found that sequences up to 50 base pairs upstream of the consensus motif significantly contributed to α-CTD (the alpha subunit carboxy-terminal domain) association. Meanwhile, two repeats of a proximal subsite were able to more strongly activate the expression (by 8.2-fold) through strengthening interactions between UP elements and RNAP. Based the above molecular basis, a synthetic UP element, UP5-2P, was constructed and applied to nine wild-type promoters. Fluorescence polarization results demonstrated that it had an apparent effect on promoter–α-CTD interactions, and elevated expression strength was observed for all the engineered promoters. The highest improved core promoter, Pacpp, was more strongly activated by 7.4-fold. This work thus develops a novel strategy for Bacillus promoter engineering.