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噬菌体P1在土壤中对大肠杆菌的转导作用

Transduction of Escherichia coli by bacteriophage P1 in soil.

作者信息

Zeph L R, Onaga M A, Stotzky G

机构信息

Department of Biology, New York University, New York 10003.

出版信息

Appl Environ Microbiol. 1988 Jul;54(7):1731-7. doi: 10.1128/aem.54.7.1731-1737.1988.

Abstract

Transduction of Escherichia coli W3110(R702) and J53(RP4) (10(4) to 10(5) CFU/g of soil) by lysates of temperature-sensitive specialized transducing derivatives of bacteriophage P1 (10(4) to 10(5) PFU/g of soil) (P1 Cm cts, containing the resistance gene for chloramphenicol, or P1 Cm cts::Tn501, containing the resistance genes for chloramphenicol and mercury [Hg]) occurred in soil amended with montmorillonite or kaolinite and adjusted to a -33-kPa water tension. In nonsterile soil, survival of introduced E. coli and the numbers of E. coli transductants resistant to chloramphenicol or Hg were independent of the clay amendment. The numbers of added E. coli increased more when bacteria were added in Luria broth amended with Ca and Mg (LCB) than when they were added in saline, and E. coli transductants were approximately 1 order of magnitude higher in LCB; however, the same proportion of E. coli was transduced with both types of inoculum. In sterile soil, total and transduced E. coli and P1 increased by 3 to 4 logs, which was followed by a plateau when they were inoculated in LCB and a gradual decrease when they were inoculated in saline. Transduction appeared to occur primarily in the first few days after addition of P1 to soil. The transfer of Hg or chloramphenicol resistance from lysogenic to nonlysogenic E. coli by phage P1 occurred in both sterile and nonsterile soils. On the basis of heat-induced lysis and phenotype, as well as hybridization with a DNA probe in some studies, the transductants appeared to be the E. coli that was added. Transduction of indigenous soil bacteria was not unequivocally demonstrated.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在添加了蒙脱石或高岭土并将水张力调节至-33 kPa的土壤中,噬菌体P1的温度敏感型特异性转导衍生物(10⁴至10⁵ PFU/g土壤)(P1 Cm cts,含有氯霉素抗性基因,或P1 Cm cts::Tn501,含有氯霉素和汞[Hg]抗性基因)的裂解物对大肠杆菌W3110(R702)和J53(RP4)(10⁴至10⁵ CFU/g土壤)进行了转导。在非无菌土壤中,引入的大肠杆菌的存活以及对氯霉素或汞具有抗性的大肠杆菌转导子数量与粘土添加物无关。当细菌添加到用钙和镁改良的Luria肉汤(LCB)中时,添加的大肠杆菌数量增加得比添加到盐水中时更多,并且在LCB中大肠杆菌转导子大约高1个数量级;然而,两种接种物转导的大肠杆菌比例相同。在无菌土壤中,总的和转导的大肠杆菌及P1增加了3至4个对数,当它们接种在LCB中时随后达到平稳期,而接种在盐水中时则逐渐减少。转导似乎主要发生在向土壤中添加P1后的最初几天。噬菌体P1将汞或氯霉素抗性从溶源型大肠杆菌转移到非溶源型大肠杆菌的过程在无菌和非无菌土壤中均发生。根据热诱导裂解和表型,以及在一些研究中与DNA探针的杂交,转导子似乎是添加的大肠杆菌。未明确证明对本地土壤细菌的转导。(摘要截短于250字)

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