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A gene from Renibacterium salmoninarum encoding a product which shows homology to bacterial zinc-metalloproteases

机译:来自展开型产品与细菌锌 - 金属蛋白酶同源性的产物的可重杆菌Sal喃喃的基因

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A genomic library constructed from Renibacterium salmoninarum isolate MT444 DNA in the plasmid vector pBR328 was screened using Escherichia coli host strain DH1 for the expression of genes encoding putative virulence factors. A single haemolytic clone was isolated at 22 °C and found to contain a 31 kb Hindlll fragment of inserted DNA. This fragment was present in seven isolates of R. salmoninarum which were examined. Western blots of extracts from clones exhibiting haemolytic activity were performed with antisera raised against either cellular or extracellular components of R. salmoninarum and failed to identify any additional proteins compared to control E. coli containing pBR328. However, minicell analysis revealed that a polypeptide with an apparent molecular mass of 65 kDa was associated with a haemolytic activity distinct from that previously described for R. salmoninarum. The nucleotide sequence of the gene encoding this product was determined and the amino acid sequence deduced. The product was 548 amino acids with a predicted molecular mass of 66757 Da and a pl of 557. The deduced amino acid sequence of the gene possessed strong similarities to those of a range of secreted bacterial zinc-metalloproteases and was tentatively designated hly. Neither protease nor lecithinase activities were detectable in E. coli recombinants expressing gene hly. Haemolytic activity was observed from 6 °C to 37 °C for erythrocytes from a number of mammalian species and also from fish. Gene hly was expressed in E. coli as a fusion protein consisting of maltose-binding protein at the N-terminus linked to all but the first 24 amino acids, largely constituting the putative signal peptide, of the N-terminus of Hly. The soluble fusion protein was produced and purified by affinity chromatography. Antiserum raised against the purified fusion protein was used to probe Western blots of cell lysates and extracellular products from seven isolates of R. salmoninarum cultured under conditions of iron-sufficiency or iron-restriction. The results indicate that the availability of iron modulates the expression of the hly gene.
机译:使用大肠杆菌宿主菌株DH1筛选从质粒载体PBR328中的可重生SalinaRum分离物MT444 DNA构建的基因组文库,用于表达编码推定毒力因子的基因。在22℃下分离单个溶血克隆,发现插入DNA的31kb HindIFL片段。该片段存在于七分离的R. Sal甘油的分离物中。用抗血清升高的抗血清抑制R. Sal喃:的细胞或细胞外组分的抗血清进行克隆的蛋白质墨水,与含有PBR328的大肠杆菌进行比较,未能鉴定任何额外的蛋白质。然而,Minicell分析显示,具有65kDa的表观分子量的多肽与从前用于R. Salominarum描述的血液解活性有关。测定编码该产物的基因的核苷酸序列,并推导出氨基酸序列。该产物是548个氨基酸,预测的分子量为66757Da,PL为557.该基因的推导氨基酸序列与一系列分泌的细菌锌金属蛋白释放酶具有强烈的相似性,并且暂时指定为HID。在表达基因的大肠杆菌重组中,均未检测到蛋白酶和卵磷脂酶活性。从许多哺乳动物物种以及来自鱼的红细胞,从6℃〜37℃观察到溶血活性。 HLY在大肠杆菌中表达的基因作为融合蛋白,其在与HLY的N-末端的第一个24个氨基酸的N-末端连接的N-末端中的麦芽糖结合蛋白组成。通过亲和层析制备和纯化可溶性融合蛋白。针对纯化的融合蛋白升高的抗血清用于探测来自在铁 - 充足或铁 - 限制的条件下培养的R. Salominarum的七分离株的细胞裂解物和细胞外产物的蛋白质印迹。结果表明铁的可用性调节了HLY基因的表达。

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