Siddiqui R A, Benthin K, Schlegel H G
Institut für Mikrobiologie, Universität Göttingen, Federal Republic of Germany.
J Bacteriol. 1989 Sep;171(9):5071-8. doi: 10.1128/jb.171.9.5071-5078.1989.
The 163-kilobase-pair (kb) plasmid pMOL28, which determines inducible resistance to nickel, cobalt, chromate, and mercury salts in its native host Alcaligenes eutrophus CH34, was transferred to a derivative of A. eutrophus H16 and subjected to cloning procedures. After Tn5 transposon mutagenesis, restriction endonuclease analysis, and DNA-DNA hybridization, two DNA fragments, a 9.5-kb KpnI fragment and a 13.5-kb HindIII fragment (HKI), were isolated. HKI contained EK1, the KpnI fragment, as a subfragment flanked on both sides by short regions. Both fragments were ligated into the suicide vector pSUP202, the broad-host-range vector pVK101, and pUC19. Both fragments restored a nickel-sensitive Tn5 mutant to full nickel and cobalt resistance. The hybrid plasmid pVK101::HKI expressed full nickel resistance in all nickel-sensitive derivatives, either pMOL28-deficient or -defective, of the native host CH34. The hybrid plasmid pVK101::HKI also conferred nickel and cobalt resistance to A. eutrophus strains H16 and JMP222, Alcaligenes hydrogenophilus, Pseudomonas putida, and Pseudomonas oleovorans, but to a lower level of resistance. In all transconjugants the metal resistances coded by pVK101::HKI were expressed constitutively rather than inducibly. The hybrid plasmid metal resistance was not expressed in Escherichia coli. DNA sequences responsible for nickel resistance in newly isolated strains showed homology to the cloned pMOL28-encoded nickel and cobalt resistance determinant.
163千碱基对(kb)的质粒pMOL28,在其天然宿主嗜碱产碱菌CH34中决定对镍、钴、铬酸盐和汞盐的诱导抗性,被转移到嗜碱产碱菌H16的一个衍生物中并进行克隆操作。经过Tn5转座子诱变、限制性内切酶分析和DNA-DNA杂交,分离出两个DNA片段,一个9.5 kb的KpnI片段和一个13.5 kb的HindIII片段(HKI)。HKI包含EK1(KpnI片段)作为两侧由短区域侧翼的亚片段。两个片段都被连接到自杀载体pSUP202、广宿主范围载体pVK101和pUC19中。两个片段都使镍敏感的Tn5突变体恢复了对镍和钴的完全抗性。杂交质粒pVK101::HKI在天然宿主CH34的所有镍敏感衍生物(无论是pMOL28缺陷型还是缺陷型)中都表达了完全的镍抗性。杂交质粒pVK101::HKI还赋予嗜碱产碱菌菌株H16和JMP222、嗜碱嗜氢菌、恶臭假单胞菌和食油假单胞菌镍和钴抗性,但抗性水平较低。在所有转接合子中,由pVK101::HKI编码的金属抗性是组成型表达而非诱导型表达。杂交质粒的金属抗性在大肠杆菌中不表达。新分离菌株中负责镍抗性的DNA序列与克隆的pMOL28编码的镍和钴抗性决定簇显示出同源性。