Open AccessEfficiency of the transfer of a pSAM2‐derivative plasmid between two strains of Streptomyces lividans in conditions ranging from agar slants to non‐sterile soil microcosms
Author(s) -
Clerc Sylvie,
Simonet Pascal
Publication year - 1996
Publication title -
fems microbiology ecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.377
H-Index - 155
eISSN - 1574-6941
pISSN - 0168-6496
DOI - 10.1111/j.1574-6941.1996.tb00343.x
Subject(s) - biology , plasmid , microcosm , microbiology and biotechnology , agar , bacteria , agar plate , strain (injury) , incubation , population , streptomyces , nutrient agar , streptomycetaceae , rhizosphere , actinomycetales , genetics , ecology , gene , biochemistry , demography , anatomy , sociology
The aim of this work was to determine the efficiency of the conjugative plasmid pTS130 to transfer in various environmental conditions between two strains of Streptomyces lividans . This plasmid is a derivative of the conjugative and integrative plasmid pSAM2 isolated originally from Streptomyces ambofaciens and capable of transfer to a large range of bacteria. Our results demonstrate the high frequency of the conjugation mechanism since more than 60% of the recipient cells developed on agar slants harbored the plasmid pTS130 (as evidenced by Southern hybridization with a pSAM2 derivative plasmid probe). When donor and recipient strains were inoculated into sterile and non‐sterile soil microcosms, transconjugants were detected after two days of incubation in both cases. However, the number of donor, recipient and transconjugant cells were established at a lower level in the non‐sterile soil than in the sterile soil experiments. Moreover, nutrient amendment of the sterile soil was found to increase the population levels of parental strains and transfer frequencies both significantly and simultaneously. On the other hand, modifying water potential of the soil microcosms did not result in affecting the establishment of the Streptomyces lividans cells or the transfer rate.