Bordenave M, Goldberg R, Huet J C, Pernollet J C
Laboratoire d'Enzymologie en Milieu Structuré, Institut Jacques Monod, Paris, France.
Phytochemistry. 1995 Jan;38(2):315-9. doi: 10.1016/0031-9422(94)00647-c.
An acetyl esterase was purified from cell walls isolated from mung bean hypocotyls. The purified enzyme had an apparent Mr of 43,300 and an apparent pI > 9. It rapidly deesterified triacetin and p-nitrophenylacetate and slowly released acetate from beet and flax pectins, the deesterification rate being increased by previous demethylation of the pectins. No significant peptide sequence identity between the acetyl esterase and any known protein could be found in protein data bases.
从绿豆下胚轴分离的细胞壁中纯化出一种乙酰酯酶。纯化后的酶表观分子量为43300,表观等电点大于9。它能迅速使三醋精和对硝基苯乙酸脱酯,并缓慢从甜菜和亚麻果胶中释放出乙酸,果胶预先脱甲基可提高脱酯速率。在蛋白质数据库中未发现该乙酰酯酶与任何已知蛋白质有明显的肽序列同一性。