Biotransformation method for L-glufosinate
A technology of biotransformation and glufosinate-ammonium, applied in the field of biotransformation of L-glufosinate-ammonium, can solve the problems of harsh processing and manufacturing process, difficult to degrade D-type glufosinate-ammonium, difficult to meet production requirements, etc., and achieve catalytic effect Good, the effect of shortening the conversion time and increasing the yield
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Embodiment 1
[0034] The preparation process of L-glufosinate-ammonium crystal comprises the steps:
[0035] The biotransformation method of L-glufosinate-ammonium, the reaction is carried out in a 1L shake flask, and the reaction system is controlled as 300mL, with 2-carbonyl-4-(hydroxymethylphosphono)butanoic acid of 30g as substrate, and MOPS buffer solution (with 3-morpholinopropanesulfonic acid and Na 2 PO 4 The normal saline solution that is the buffer pair) is solvent, with the glufosinate-ammonium dehydrogenase that derives from Saccharomyces cerevisiae of 22g / L, the whole cell of the genetically engineered bacteria that derives from the co-expression of formate dehydrogenase of Candida boidinii is catalyst, add 60g ammonium formate, an appropriate amount of coenzyme NADP+ and 0.165g additive for conversion reaction, adding to obtain a conversion solution containing L-glufosinate-ammonium. Wherein, the additive is a mixture of 0.1238g of apple extract powder and 0.0412g of spiruli...
Embodiment 2
[0038] The preparation process of L-glufosinate-ammonium crystal comprises the steps:
[0039] The biotransformation method of L-glufosinate-ammonium, the reaction is carried out in a 1L shake flask, and the reaction system is controlled as 300mL, with 30g of 2-carbonyl-4-(hydroxymethylphosphono)butanoic acid as substrate, and carbonate The buffer solution is used as a solvent, with 25g / L of glufosinate-ammonium dehydrogenase derived from Saccharomyces cerevisiae and the whole cell of genetically engineered bacteria co-expressed with formate dehydrogenase derived from Candida boidinii as a catalyst, 60g of ammonium formate is added, and an appropriate amount of coenzyme NADP+ and 0.375g of additives were converted into a conversion solution containing L-glufosinate-ammonium. Wherein, the additive is a mixture of 0.3g of apple extract powder and 0.075g of spirulina powder. The preparation method of the apple extract powder is as follows: crushing fresh apples, squeezing the ju...
Embodiment 3
[0042] The preparation process of L-glufosinate-ammonium crystal comprises the steps:
[0043] The biotransformation method of L-glufosinate-ammonium, the reaction is carried out in a 1L shake flask, and the reaction system is controlled as 300mL, with 30g of 2-carbonyl-4-(hydroxymethylphosphono)butanoic acid as substrate, buffered with phosphate The solution is used as a solvent, and 20 g / L of glufosinate-ammonium dehydrogenase derived from Saccharomyces cerevisiae and whole cells of genetically engineered bacteria co-expressed with formate dehydrogenase derived from Candida boidinii are used as catalysts, and 60 g of ammonium formate is added, and an appropriate amount of coenzyme NADP+ Perform transformation reaction with 0.18g additive to obtain transformation liquid containing L-glufosinate-ammonium. Wherein, the additive is a mixture of 0.15g of apple extract powder and 0.03g of spirulina powder. The preparation method of the apple extract powder is as follows: crush fr...
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