Poole K, Heinrichs D E, Neshat S
Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada.
Mol Microbiol. 1993 Nov;10(3):529-44. doi: 10.1111/j.1365-2958.1993.tb00925.x.
Pseudomonas aeruginosa strain K437 is defective in the production of a 90kDa ferripyoverdine receptor and is unable to grow in an iron-deficient medium in the presence of the non-metabolizable iron chelator 2,2'-dipyridyl (0.25 mM). An attempt to clone the ferripyoverdine receptor gene was made by complementing this growth defect. A number of clones restoring growth of K437 on dipyridyl-containing medium were obtained and several of these restored moderate expression of the 90 kDa receptor. A 5.5 kb xhoI-HindIII fragment derived from one of these clones was similarly capable of complementing the dipyridyl growth defect although it failed to restore expression of the 90 kDa ferripyoverdine receptor. Nucleotide sequencing of the 5.5 kb fragment revealed two large open reading frames (ORFs), designated ORFA and ORFB, which appeared to form an operon and were capable of encoding products of 41 kDa and 112 kDa, respectively. Using a phage T7-based expression system, products of 42 kDa and c. 108 kDa were produced from the cloned DNA, confirming that the ORFs were, indeed, expressed. The cloned ORFAB operon was inducible under conditions of iron limitation in both P. aeruginosa and Escherichia coli. In addition, mutants expressing ORFAB constitutively were constitutive for pyoverdine and ferripyoverdine receptor production suggesting that components of the pyoverdine-mediated iron-transport system are co-regulated with ORFAB. The predicted products of ORFA and ORFB showed significant homology to the Escherichia coli EnvC and EnvD polypeptides which are reportedly involved in septum formation. In addition, the ORFB product showed moderate homology to the CzcA polypeptide identified as a component of a membrane-associated plasmid-encoded cation efflux system in Alcaligenes eutrophus. Using in vitro mutagenesis and gene replacement, ORFA- and ORFB-deficient mutants of K372, the parent strain of K437, were constructed. These mutants were unable to grow on iron-deficient minimal medium containing 0.25 mM dipyridyl although they expressed the ferripyoverdine receptor and were proficient in pyoverdine-mediated iron uptake. Despite the homology of the ORFA and ORFB products to EnvC and EnvD, respectively, the ORFA-ORFB-deficient mutants were not defective in septum formation.(ABSTRACT TRUNCATED AT 400 WORDS)
铜绿假单胞菌K437菌株在产生一种90kDa的铁载体受体方面存在缺陷,并且在不可代谢的铁螯合剂2,2'-联吡啶(0.25 mM)存在的情况下,无法在缺铁培养基中生长。通过弥补这种生长缺陷来尝试克隆铁载体受体基因。获得了许多能使K437在含联吡啶培养基上恢复生长的克隆,其中一些克隆使90kDa受体恢复了适度表达。源自其中一个克隆的5.5 kb XhoI-HindIII片段同样能够弥补联吡啶生长缺陷,尽管它未能恢复90kDa铁载体受体的表达。对该5.5 kb片段进行核苷酸测序,发现了两个大的开放阅读框(ORF),分别命名为ORFA和ORFB,它们似乎形成一个操纵子,分别能够编码41kDa和112kDa的产物。使用基于噬菌体T7的表达系统,从克隆的DNA中产生了42kDa和约108kDa的产物,证实这些ORF确实得到了表达。克隆的ORFAB操纵子在铜绿假单胞菌和大肠杆菌的铁限制条件下均可诱导表达。此外,组成型表达ORFAB的突变体在铁载体和铁载体受体产生方面是组成型的,这表明铁载体介导的铁转运系统的组分与ORFAB共同受到调控。ORFA和ORFB的预测产物与据报道参与隔膜形成的大肠杆菌EnvC和EnvD多肽具有显著同源性。此外,ORFB产物与在嗜碱产碱杆菌中被鉴定为膜相关质粒编码的阳离子外排系统组分的CzcA多肽具有适度同源性。利用体外诱变和基因置换技术,构建了K437的亲本菌株K372的ORFA 和ORFB缺陷型突变体。这些突变体无法在含有0.25 mM联吡啶的缺铁基本培养基上生长,尽管它们表达铁载体受体并且在铁载体介导的铁摄取方面表现正常。尽管ORFA和ORFB产物分别与EnvC和EnvD具有同源性,但ORFA - ORFB缺陷型突变体在隔膜形成方面并无缺陷。(摘要截短于400字)