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Truncated type IV pilin PilA(108) activates the intramembrane protease AlgW to cleave MucA and PilA(108) itself in vitro

机译:截短的IV型菌毛蛋白PilA(108)在体外激活膜内蛋白酶AlgW裂解MucA和PilA(108)本身

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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
机译:为了在铜绿假单胞菌中产生藻酸盐,必须激活膜内蛋白酶AlgW才能切割抗σ因子MucA的周质结构域,以释放螯合的ECFσ因子AlgU。以前,我们报道了pilA基因中的三个串联点突变,导致被称为PilA(108)的C型端基为苯丙氨酸-苏氨酸-苯丙氨酸(FTF)的截短的IV型菌毛诱导了PAO579菌株的粘液性。在这项研究中,我们纯化了PilA(108)蛋白并合成了对应于PilA108 C端的肽'SGAGDITFTF',发现它们都引起AlgW降解MucA。有趣的是,AlgW还可以在丙氨酸(62)和甘氨酸(63)残基之间切割PilA(108)。过度表达带有重组FTF基序的MucE蛋白,原本是小的周质蛋白

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