alr (alanine racemase)-deficient lactobacillus plantarum NC8
A technology of Lactobacillus plantarum and ems-alr-emx, applied in plant genetic improvement, botany equipment and methods, bacteria, etc., can solve problems such as biological safety hazards, affecting gene expression, and application value limitations
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Embodiment 1
[0037] Example 1 Construction of alanine racemase gene alr deletion suicide plasmid pNZ5319-Δalr
[0038] 1. Main experimental materials and molecular biology reagents
[0039] (1) Strains and plasmid vectors
[0040] Lactobacillus plantarum NC8 strain was donated by senior researcher Anbazhagan.K of Kamaraj University in India; Escherichia coli JM109 was preserved by our laboratory; plasmids pNZ5319 and pNZ5348 were donated by Dr. Ingridvan Alen of NIZOfoodresearch; pET41a vector was provided by Novagen; pCJ1 (pSIP409), preserved by our laboratory.
[0041] (2) Main materials and reagents
[0042] Gram-positive bacterial genome extraction kit, plasmid mini-extraction kit, gel recovery kit, PCR product recovery kit are provided by Beijing Tiangen Biotechnology Company; high-fidelity PCR polymerase, restriction endonuclease, T4DNA ligase Provided by Takara Company; electric cup provided by Bio-Rad Company; erythromycin and chloramphenicol provided by Sigma; other main reage...
Embodiment 2
[0099] Example 2 Construction of alanine racemase gene alr marker plasmid expression vector pCJ2
[0100] In order to replace the erythromycin marker gene on the pCJ1 vector without mutation, the 343 bp of the upper arm end of the erythromycin gene (including the restriction site BamHI) on the pCJ1 vector, the 1128 bp of the alr gene, and the erythromycin gene on the pCJ1 vector were respectively amplified by PCR. The 567bp fragment at the downstream arm end of the gene (including the enzyme cutting site ClaI), after the PCR product was recovered and purified, the EmSF and EmXR primers were added and the three fragments were connected by SOE-PCR single-tube reaction to obtain the EmS-alr-EmX fragment with a base sequence of 2038bp . After subcloning, the linked fragment was double-digested with BamHI and ClaI, and the digested product was recovered, purified and quantified, linked with the pCJ1 fragment double-digested with the same enzyme, and transformed into the alanine-defic...
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