Gireesh T, Davidson B E, Hillier A J
Russell Grimwade School of Biochemistry, University of Melbourne, Parkville, Victoria, Australia.
Appl Environ Microbiol. 1992 May;58(5):1670-6. doi: 10.1128/aem.58.5.1670-1676.1992.
Nisin-producing transconjugants were generated by mating nisin-producing strains of Lactococcus lactis subsp. lactis with derivatives of L. lactis subsp. lactis LM0230. The sucrose-utilizing ability and reduced bacteriophage sensitivity were also transferred with the nisin-producing character. Pulsed-field gel electrophoretic analysis of genomic DNA from donor, recipient, and nisin-producing transconjugants indicated that 68 kbp of DNA was transferred from the chromosome of the donor into the chromosome of the recipient in the conjugation process. The location of the transferred nisin structural gene spaN in the transconjugant HID500 was not stable, and cultures of strain HID500 were a mixture of different genotypes in which spaN was located at different positions in the chromosome on different SmaI fragments. ApaI, BglI, BssHII, NciI, SalI, and SmaI digests of genomic DNA were used to map the location of spaN in a donor (DL11) and a nisin-producing transconjugant (HID504).
通过将乳酸乳球菌乳酸亚种的产乳链菌肽菌株与乳酸乳球菌乳酸亚种LM0230的衍生物进行接合,产生了产乳链菌肽的接合子。利用蔗糖的能力和降低的噬菌体敏感性也与产乳链菌肽特性一起转移。对供体、受体和产乳链菌肽的接合子的基因组DNA进行脉冲场凝胶电泳分析表明,在接合过程中,68 kbp的DNA从供体染色体转移到受体染色体。在接合子HID500中,转移的乳链菌肽结构基因spaN的位置不稳定,HID500菌株的培养物是不同基因型的混合物,其中spaN位于染色体上不同SmaI片段的不同位置。基因组DNA的ApaI、BglI、BssHII、NciI、SalI和SmaI酶切用于在供体(DL11)和产乳链菌肽的接合子(HID504)中定位spaN的位置。