摘要:
The present invention provides compositions and methods of treating hyperphenylalaninemia (e.g., phenylketonuria) in a subject in need thereof comprising administering to the subject an effective amount of a phenylalanine dehydrogenase (PheDH) polypeptide. The present invention also provides pharmaceutical formulations comprising PheDH for lowering the phenylalanine concentration in the subject (e.g., in the intestines and/or blood).
摘要:
A synthesis method for L-heterocyclic amino acid and a pharmaceutical composition thereof are provided. The method comprises: step a.) preparing heterocyclic keto acid, wherein the heterocycle of the heterocyclic keto acid is selected from a five-membered heterocycle, a six-membered heterocycle, a seven-membered heterocycle, an alkyl-substituted five-membered heterocycle, an alkyl-substituted six-membered heterocycle, and an alkyl-substituted seven-membered heterocycle; step b.) mixing the heterocyclic keto acid with ammonium formate, phenylalanine dehydrogenase, formate dehydrogenase and coenzyme NAD+ to generate L-heterocyclic amino acid, wherein the phenylalanine dehydrogenase amino acid sequence is SEQ ID No. 1. The synthesis method allows for a high conversion rate of raw materials and high chiral selectivity.
摘要翻译:提供了一种L-杂环氨基酸的合成方法及其药物组合物。 该方法包括:步骤a)制备杂环酮酸,其中杂环酮酸的杂环选自五元杂环,六元杂环,七元杂环,烷基取代的五元杂环 ,烷基取代的六元杂环和烷基取代的七元杂环; 步骤b)将杂环酮酸与甲酸铵,苯丙氨酸脱氢酶,甲酸脱氢酶和辅酶NAD +混合以产生L-杂环氨基酸,其中苯丙氨酸脱氢酶氨基酸序列是SEQ ID No.1。合成方法允许高 原料转化率高,手性选择性高。
摘要:
The present invention provides a process for producing a vinylglycine derivative represented by the formula (2): wherein R 1 represents hydrogen, an alkyl group having 1 to 8 carbon atoms, or an aryl group having 6 to 20 carbon atoms; or a salt thereof comprising a step of reacting in the presence of an ammonium salt compound and a cofactor a vinyl glyoxylic acid represented by the formula (1): wherein R 1 is the same as defined above; or a salt thereof with an amino acid dehydrogenase, a culture of a microorganism capable of producing an amino acid dehydrogenase or a processed product of the culture, etc.
摘要:
The present invention relates to a novel biocatalytic method for the production of primary and secondary amines, comprising coupled enzymatic oxidation and reduction processes simultaneously regenerating the required cofactor; making use of two enzymes - i.e. an alcohol dehydrogenase and an amine dehydrogenase - operating simultaneously in a one pot process (i.e. biocatalytic cascade). Furthermore, the overall process is redox neutral, since the hydride generated from the first oxidative step is internally recycled in the second reductive step. The invention also relates to recombinant expression systems and microorganisms procuring the required enzyme activities; and bioreactors for performing such methods.