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由辅酶PQQ与各种氨基酸合成的咪唑并吡咯喹啉化合物的表征

Characterization of imidazopyrroloquinoline compounds synthesized from coenzyme PQQ and various amino acids.

作者信息

Urakami T, Sugamura K, Niki E

机构信息

Biochemicals Division, Mitsubishi Gas Chemical Co., Tokyo, Japan.

出版信息

Biofactors. 1995;5(2):75-81.

PMID:8722120
Abstract

Imidazopyrroloquinoline (IPQ) compounds synthesized from coenzyme PQQ (pyrroloquinoline quinone) and various kinds of amino acids were characterized. IPQ was synthesized from coenzyme PQQ and one of three amino acids (glycine, L-tryptophan and L-tyrosine). Two kinds of IPQ compound were formed from coenzyme PQQ and L-serine. At higher pH, IPQ was synthesized, at lower pH hydroxy-methyl-IPQ was synthesized. IPQ with R of amino acids represented by R-CH(NH2)-COOH was synthesized from coenzyme PQQ and other amino acids. IPQ compounds do not act as cofactor of glucose dehydrogenase. Molar absorption coefficients of IPQ are 31,400 M-1 cm-1 at 251 nm, 30,700 M-1 cm-1 at 276 nm, and 20,700 M-1 cm-1 at 423 nm at pH 7.0 and room temperature.

摘要

对由辅酶PQQ(吡咯并喹啉醌)与各种氨基酸合成的咪唑并吡咯喹啉(IPQ)化合物进行了表征。IPQ由辅酶PQQ与三种氨基酸(甘氨酸、L-色氨酸和L-酪氨酸)之一合成。由辅酶PQQ和L-丝氨酸形成了两种IPQ化合物。在较高pH值下合成IPQ,在较低pH值下合成羟甲基-IPQ。由辅酶PQQ和其他氨基酸合成了氨基酸R以R-CH(NH2)-COOH表示的IPQ。IPQ化合物不作为葡萄糖脱氢酶的辅因子。在pH 7.0和室温下,IPQ在251 nm处的摩尔吸收系数为31400 M-1 cm-1,在276 nm处为30700 M-1 cm-1,在423 nm处为20700 M-1 cm-1。

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