Kleineidam R G, Furuhata K, Ogura H, Schauer R
Biochemisches Institut Universität zu Kiel, Germany
Biol Chem Hoppe Seyler. 1990 Aug;371(8):715-9. doi: 10.1515/bchm3.1990.371.2.715.
4-O-Acetylated, 7-O-acetylated, and 9-O-acetylated 4-methylumbelliferyl-alpha-N-acetyl-neuraminic acids (Neu4,5Ac2-MU, Neu5,7Ac2-MU, Neu5,9Ac2-MU) were tested as substrates of sialidases of Vibrio cholerae and of Clostridium perfringens. Both sialidases were unable to hydrolyse Neu4,5Ac2-MU. This compound at 1 mM concentration did not inhibit significantly the cleavage of Neu5Ac-MU, the best substrate tested. The 4-O-acetylated sialic acid glycoside is hydrolysed slowly by the sialidase from fowl plague virus. The relative substrate specificity, reflected in V/Km of the Vibrio cholerae sialidase is Neu5Ac-MU much greater than Neu5,7Ac2-MU approximately Neu5,9Ac2-MU and of the clostridial enzyme it is Neu5Ac-MU greater than Neu5,9Ac2-MU greater than Neu5,7Ac2-MU. The affinities of both enzymes for the side-chain O-acetylated sialic acid derivatives are higher than for Neu5Ac-MU. The artificial, well-defined substrates, described here, provide the opportunity to quantify the influence of sialic acid O-acetylation on the hydrolysis of sialoglycoconjugates without the side effects introduced by other parts of more complex glycans.
4-O-乙酰化、7-O-乙酰化和9-O-乙酰化的4-甲基伞形酮基-α-N-乙酰神经氨酸(Neu4,5Ac2-MU、Neu5,7Ac2-MU、Neu5,9Ac2-MU)作为霍乱弧菌和产气荚膜梭菌唾液酸酶的底物进行了测试。两种唾液酸酶均无法水解Neu4,5Ac2-MU。该化合物在1 mM浓度下对Neu5Ac-MU(测试的最佳底物)的裂解没有显著抑制作用。4-O-乙酰化唾液酸糖苷被禽瘟病毒的唾液酸酶缓慢水解。霍乱弧菌唾液酸酶的V/Km反映出其相对底物特异性为Neu5Ac-MU远大于Neu5,7Ac2-MU约等于Neu5,9Ac2-MU,而梭菌酶的相对底物特异性为Neu5Ac-MU大于Neu5,9Ac2-MU大于Neu5,7Ac2-MU。两种酶对侧链O-乙酰化唾液酸衍生物的亲和力均高于对Neu5Ac-MU的亲和力。本文所述的人工合成、定义明确的底物为量化唾液酸O-乙酰化对唾液酸糖缀合物水解的影响提供了机会,而不会受到更复杂聚糖其他部分引入的副作用的影响。