Ren Z, Jin H, Morton D J, Stull T L
Departments of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, USA.
Infect Immun. 1998 Oct;66(10):4733-41. doi: 10.1128/IAI.66.10.4733-4741.1998.
Haemophilus influenzae requires heme for growth and can utilize both hemoglobin and hemoglobin-haptoglobin as heme sources. We previously identified a hemoglobin- and hemoglobin-haptoglobin-binding protein, HgpA, in H. influenzae HI689. Mutation of hgpA did not affect binding or utilization of either heme source. The hgpA mutant exhibited loss of a 120-kDa protein and increased expression of a 115-kDa protein. These data suggested that at least one other gene product is involved in binding of these heme sources by H. influenzae. A 3.2-kbp PCR product derived from HI689 was cloned. The nucleotide sequence indicated a separate, distinct gene with high homology to hgpA, which would encode a 115-kDa protein. Primers were designed for directional cloning of the structural gene in the correct reading frame. Sonicates of induced Escherichia coli harboring the cloned open reading frame bound both hemoglobin and hemoglobin-haptoglobin. An insertion/deletion mutant of H. influenzae at the newly identified locus, designated hgpB, was constructed. The 115-kDa protein was not detected in the mutant after affinity purification using biotinylated hemoglobin. An hgpA hgpB double-mutant strain exhibited a reduced ability to utilize hemoglobin-haptoglobin, although it was unaltered in the ability to utilize hemoglobin. Affinity isolation of hemoglobin-binding proteins from the double mutant resulted in isolation of an approximately 120-kDa protein. Internal peptide sequencing revealed this protein to be a third distinct protein, highly homologous to HgpA and HgpB. In summary a second hemoglobin- and hemoglobin-haptoglobin-binding protein of H. influenzae has been identified and characterized, and the presence of an additional protein of similar function has been revealed.
流感嗜血杆菌生长需要血红素,并且能够利用血红蛋白和血红蛋白 - 结合珠蛋白作为血红素来源。我们之前在流感嗜血杆菌HI689中鉴定出一种血红蛋白和血红蛋白 - 结合珠蛋白结合蛋白HgpA。hgpA突变不影响任何一种血红素来源的结合或利用。hgpA突变体表现出一种120 kDa蛋白的缺失以及一种115 kDa蛋白的表达增加。这些数据表明,至少还有一种其他基因产物参与流感嗜血杆菌对这些血红素来源的结合。从HI689获得的一个3.2 kbp的PCR产物被克隆。核苷酸序列表明存在一个与hgpA具有高度同源性的单独、独特的基因,该基因将编码一种115 kDa的蛋白。设计引物用于在正确的阅读框中定向克隆结构基因。携带克隆的开放阅读框的诱导型大肠杆菌的超声裂解物能结合血红蛋白和血红蛋白 - 结合珠蛋白。构建了流感嗜血杆菌在新鉴定位点(命名为hgpB)的插入/缺失突变体。使用生物素化血红蛋白进行亲和纯化后,在该突变体中未检测到115 kDa的蛋白。hgpA hgpB双突变菌株利用血红蛋白 - 结合珠蛋白的能力降低,尽管其利用血红蛋白的能力未改变。从双突变体中亲和分离血红蛋白结合蛋白得到一种约120 kDa的蛋白。内部肽段测序表明该蛋白是第三种独特的蛋白,与HgpA和HgpB高度同源。总之,已鉴定并表征了流感嗜血杆菌的第二种血红蛋白和血红蛋白 - 结合珠蛋白结合蛋白,并揭示了另一种具有相似功能的蛋白的存在。