Streptococcus broad-spectrum chimeric lyase GBS-V12b and coding gene and application thereof
A streptococcus and lyase technology, applied in the field of genetic engineering, can solve problems such as mixed bacterial infection and narrow lysis spectrum, and achieve high stability and wide application prospects
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Embodiment 1
[0027] Embodiment 1: Construction of broad-spectrum streptococcus chimeric lyase
[0028] 1. Preparation of the catalytic domain of PlyGBS and the cell wall binding domain of PlyV12
[0029] The full-sequence synthesis of lyase PlyGBS and lyase PlyV12 (Nanjing GenScript Biotechnology Co., Ltd.), and the synthetic sequence was loaded into the pUC57 plasmid. Using the plyGBS gene as a template and GBS180-F / GBS180-R as primers, the sequence of the catalytic domain GBS180 of PlyGBS was amplified; using the PlyV12 gene as a template and V12b-F / V12b-R as primers, the cell wall binding of PlyV12 was amplified area. The primers and restriction site information used in the clone construction are as follows:
[0030] GBS180-F:5-TTAA CCATGG GCATGGCTACCTACCAGG-3
[0031] GBS180-R:5-TATA GGATCC GATCGTTTTGGTCGTGC-3
[0032] V12b-F:5-ATAT GGATCC TTAAACGGTGGAAGCAC-3
[0033] V12b-R:5-TATA CTCGAG CTTAAATGTACCCCATG-3
[0034] GBS180-F primers underline the restriction endonuclease...
Embodiment 2
[0041] Example 2: Verification of GBS-V12b killing Streptococcus dysgalactiae standard strain ATCC 35666
[0042] Cultivate Streptococcus dysgalactiae overnight, collect by centrifugation, wash once with PBS, then dissolve in PBS, and adjust the OD of the bacteria solution 600nm =0.6~0.8. Take 0.01mL of GBS-V12b in Example 1 and mix it with 0.19mL of the above bacterial solution, and monitor the change of the absorption value of the mixture at 600nm with a microplate reader. At the same time, a mixture of 0.01 mL of PBS buffer solution and 0.19 mL of Streptococcus dysgalactiae was used as a negative control. The final cracking curve obtained is figure 2 As shown, the two curves respectively represent the OD after Streptococcus dysgalactiae was mixed with the buffer 600 The trend of change over time and OD after mixing Streptococcus dysgalactiae and GBS-V12b 600 The trend of change over time, the results show that GBS-V12b can rapidly lyse the ATCC 35666 strain, resulting ...
Embodiment 3
[0043] Example 3, GBS-V12b broad-spectrum verification of killing streptococci in vitro
[0044] Various strains of Streptococcus, Staphylococcus aureus, Enterococcus and Escherichia coli were cultured overnight, collected by centrifugation, washed once with PBS and then dissolved in PBS, and adjusted to OD600nm=0.6-0.8. Take 0.01mL of GBS-V12b and 0.19mL of the above-mentioned bacterial solution, mix and incubate at 37°C for 60min, and monitor the change of the absorption value of the mixture at 600nm with a microplate reader. The lysis effect of different strains is indicated by the value of OD600 reduction. At the same time, the mixed solution of 0.01mL PBS buffer solution and 0.19mL bacterial solution was used as a negative control, and the killing effect obtained by the test was as follows: image 3 shown. The results show that GBS-V12b can quickly kill a variety of streptococci (including Streptococcus pneumoniae, Streptococcus pyogenes, Streptococcus suis, Streptococc...
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