Sauber K, Müller R, Keller E, Eberspächer J, Lingens F
Z Naturforsch C Biosci. 1977 Jul-Aug;32(7-8):557-62.
Bacteria with the ability to grow on pyrazon as sole source of carbon were isolated from soil. They also are able to grow on antipyrin. Then three metabolites of antipyrin can be isolated from the culture fluid which were identified as 2,3-dimethyl-1-(cis-2,3-dihydro-2,3-dihydroxy-4,6-cyclohexadiene-1-yl)-pyrazolone (5) (I), as 2,3-dimethyl-1-(2,3-dihydroxyphenyl)-pyrazolone (5) (II) and as 2,3-dimethyl-pyrazolone (5) (III), respectively. Compound I and II were used as substrates for enzyme studies. A dioxygenase catalyzes the enzymatic conversion of antipyrin into compound I. In the presence of NAD as cosubstrate compound I is transformed into compound II by a dehydrogenase. A pure preparation of metapyrocatechase from pyrazon-degrading bacteria converts compound II into the dephenylated heterocyclic moiety of antipyrin (III) and into 2-pyrone-6-carboxylic acid. Based on the results of the enzymatic studies a pathway for the degradation of antipyrin is proposed.
从土壤中分离出了能够以吡唑酮作为唯一碳源生长的细菌。它们也能够在安替比林上生长。然后可以从培养液中分离出安替比林的三种代谢产物,分别鉴定为2,3-二甲基-1-(顺式-2,3-二氢-2,3-二羟基-4,6-环己二烯-1-基)-吡唑啉酮(5)(I)、2,3-二甲基-1-(2,3-二羟基苯基)-吡唑啉酮(5)(II)和2,3-二甲基-吡唑啉酮(5)(III)。化合物I和II用作酶研究的底物。一种双加氧酶催化安替比林酶促转化为化合物I。在作为共底物的NAD存在下,化合物I通过脱氢酶转化为化合物II。从吡唑酮降解细菌中获得的间苯二酚酶纯制剂将化合物II转化为安替比林的脱苯基杂环部分(III)和2-吡喃-6-羧酸。基于酶研究的结果,提出了安替比林的降解途径。