Byrd J J, Leahy J G, Colwell R R
Department of Microbiology, University of Maryland, College Park 20742.
Appl Environ Microbiol. 1992 Jul;58(7):2266-70. doi: 10.1128/aem.58.7.2266-2270.1992.
The concentration of plasmid pBR322 DNA in nonculturable Escherichia coli JM83 was measured to determine whether the plasmid concentration changed during survival of E. coli in marine and estuarine water. E. coli JM83 containing the plasmid pBR322 was placed in both sterile seawater and sterile estuarine water and analyzed for survival (i.e., culturability) and plasmid maintenance. The concentration of pBR322 DNA remained stable in E. coli JM83 for 28 days in an artificial seawater microcosm, even though nonculturability was achieved within 7 days. E. coli JM83 incubated in sterile natural seawater or sterile estuarine water did not reach nonculturability within 30 days. Under all three conditions, plasmid pBR322 DNA was maintained at approximately the initial concentration. Cloning of DNA into the plasmid pUC8 did not alter the ability of E. coli to maintain vector plasmid DNA, even when the culture was in the nonculturable state, but the concentration of plasmid DNA decreased with time in the microcosm. We conclude that E. coli is able to maintain plasmid DNA while in the nonculturable state and that the concentration at which the plasmid is maintained appears to be dependent upon the copy number of the plasmid and/or the presence of foreign DNA.
为了确定在海洋和河口水中大肠杆菌存活期间质粒浓度是否发生变化,对不可培养的大肠杆菌JM83中的质粒pBR322 DNA浓度进行了测定。将含有质粒pBR322的大肠杆菌JM83置于无菌海水和无菌河口水体中,并分析其存活情况(即可培养性)及质粒维持情况。在人工海水微观生态系统中,尽管在7天内就达到了不可培养状态,但pBR322 DNA的浓度在大肠杆菌JM83中28天内保持稳定。在无菌天然海水或无菌河口水体中培养的大肠杆菌JM83在30天内未达到不可培养状态。在所有三种条件下,质粒pBR322 DNA均维持在大约初始浓度。将DNA克隆到质粒pUC8中并不会改变大肠杆菌维持载体质粒DNA的能力,即使培养物处于不可培养状态,不过在微观生态系统中质粒DNA的浓度会随时间降低。我们得出结论,大肠杆菌在不可培养状态下能够维持质粒DNA,且维持的质粒浓度似乎取决于质粒的拷贝数和/或外源DNA的存在。