Research
| Title： | Truncated type IV pilin PilA(108) activates the intramembrane protease AlgW to cleave MucA and PilA(108) itself in vitro |
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| First author： | Li, Ronghui; Withers, Ryan T.; Dai, Jingcheng; Ruan, Jing; Li, Wei; Dai, Yujun; An, Weixing; Yu, Dianzhen; Wei, Hehong; Xia, Ming; Tian, Chunyuan; Yu, Hongwei D.; Qiu, Dongru |
| Journal： | ARCHIVES OF MICROBIOLOGY |
| Years： | 2016 |
| DOI： | 10.1007/s00203-016-1248-y |
| Abstract： | For alginate production in Pseudomonas aeruginosa, the intramembrane protease AlgW must be activated to cleave the periplasmic domain of anti-sigma factor MucA for release of the sequestered ECF sigma factor AlgU. Previously, we reported that three tandem point mutations in the pilA gene, resulting in a truncated type IV pilin termed PilA(108) with a C-terminal motif of phenylalanine-threonine-phenylalanine (FTF), induced mucoidy in strain PAO579. In this study, we purified PilA(108) protein and synthesized a peptide 'SGAGDITFTF' corresponding to C-terminus of PilA108 and found they both caused the degradation of MucA by AlgW. Interestingly, AlgW could also cleave PilA(108) between alanine(62) and glycine(63) residues. Overexpression of the recombinant FTF motifbearing MucE protein, originally a small periplasmic |
