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Colonization of gfp-tagged Lysobacter sp. SNNU513 on Maize's Root

WU Kunyi1, WANG Feifei1, CUI Langjun1, ZHANG Huawei2, BAI Chengke1   

  1. 1. Key Laboratory of Medicinal Plant Resources and Natural Pharmaceutical Chemistry, Ministry of Education/College of Life Sciences, Shaanxi Normal University, Xi'an 710062;2. School of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, China
  • Received:2012-11-08 Revised:1900-01-01 Online:2014-02-08 Published:2014-02-08

Abstract: Lysobacter sp. SNNU513 isolated from Radix polygalae rhizospher could inhibit pathogenic fungus. In this study, the preparation of the efficient competent cells were screened out and pGLO plasmid was introduced into the competent cells by electroporation and transformation. The results showed that the recombinant strain SNNU513-pGLO could efficiently and stably express the green fluorescent protein gene (gfp) when the electric field strength was 20 kV/cm and the electric pulse time was 5 ms. The percent of the green cells was 100% when the strain SNNU513-pGLO was recirculated in the non-selective medium for 20 times. Both strains SNNU513-pGLO and SNNU513 showed the same growth characteristics and the same inhibition of Rhizotonia cerealis in vivo. The gene gfp was transferred into original strain Lysobacter sp. SNNU513 by electroporation successfully. The gfp-tagged strain adhering more tightly to the velamen than the phloem could colonize on the surface and interior of maize's root.

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