Fumonisin-degrading enzyme fumdsb and its gene and application
A technology for fumonisins and degrading enzymes, applied in the field of agricultural biology, can solve the problems of changing the quality and flavor of food, high requirements, and large limitations of chemical methods, and achieve the effect of reducing harm
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Embodiment 1
[0038] Example 1 Obtaining Fumonisin Degrading Enzyme FumDSB Gene
[0039] The gene fragment derived from Sphingomonadales Bacterium fumonisin degrading enzyme FumDSB was obtained by artificial chemical synthesis, and the endonuclease site EcoR I was introduced at the 5' end, and the endonuclease site Xho I was introduced at the 3' end.
Embodiment 2
[0040] Example 2 Preparation of Fumonisin Degrading Enzyme FumDSB
[0041] The expression vector pET28a was subjected to double enzyme digestion (EcoR I+Xho I), and at the same time, the gene FumDSB encoding mature fumonisin degrading enzyme was double enzyme digested (EcoR I+Xho I), and the gene fragment encoding the degrading enzyme and the expression vector were cut out The pET28a was ligated to obtain the recombinant plasmid pET28a-FumDSB containing the degrading enzyme FumDSB and transformed into Escherichia coli BL21(DE3) to obtain the recombinant Escherichia coli strain BL21(DE3) / FumDSB.
[0042] The recombinant expression vector of fumonisin degrading enzyme gene containing signal peptide sequence was constructed in the same way.
[0043] Take the BL21(DE3) strain containing the recombinant plasmid, inoculate it in 100mL LB culture medium, shake it at 220rpm at 37℃ for 2-3h, and the OD 600 When the temperature is 0.6-0.8, add IPTG with a final concentration of 1 mM, i...
Embodiment 3
[0044] Example 3 Determination of the properties of fumonisin degrading enzyme FumDSB
[0045] The enzyme activity of fumonisin degrading enzyme is detected by high performance liquid chromatography, and the specific method is as follows:
[0046] (1) FB1 standard stock solution: Weigh 1mg of the standard product, dissolve it in 10ml of acetonitrile and water (1:1), prepare a standard solution with a concentration of 100ug / mL, and store at -20°C.
[0047] (2) Sample preparation: Take 900ul of purified fumonisin degrading enzyme enzyme solution, add 100ul of FB1 standard stock solution to make the final concentration of FB1 10ug / ml, incubate at 37°C, 220rpm, in the dark for 20min.
[0048] (3) Sample derivatization: take 100 ul of the sample to be tested, add 400 ul of 50% acetonitrile water, 500 ul of OPA derivatization solution, mix for 30 s, inject the sample within 2 min of derivatization, and filter the membrane for testing. The enzymatic activity of the fumonisin-degradi...
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