Christensen U
University of Copenhagen, Department of Chemistry, Denmark.
Eur J Biochem. 1994 Feb 15;220(1):149-53. doi: 10.1111/j.1432-1033.1994.tb18609.x.
The pH dependencies of serine carboxypeptidase-Y-catalysed hydrolysis and aminolysis reactions using L-amino acids and L-amino acid amides as nucleophiles, have been studied and analyzed. The results reveal two catalytically important ionizing groups of the enzyme with rather similar pK values (5-6), the active site His397 and a possibly Glu residue, which is not only important in interactions with carboxylic groups of substrates and nucleophiles [Liao, D.-I., Breddam, K., Sweet, R. M., Bullock, T. & Remmington, S. J. (1992) Biochemistry 31, 9796-9812], but also indirectly play a role in catalysis. This explains the pH behaviour of hydrolysis of both peptide and ester substrates and further, that L-amino acid amides are better nucleophiles in aminolysis reactions than L-amino acids.
以L-氨基酸和L-氨基酸酰胺作为亲核试剂,对丝氨酸羧肽酶Y催化的水解反应和氨解反应的pH依赖性进行了研究和分析。结果揭示了该酶的两个具有相似pK值(5-6)的对催化作用至关重要的电离基团,即活性位点His397和一个可能的Glu残基,该残基不仅在与底物和亲核试剂的羧基相互作用中很重要[廖,D.-I.,布雷德达姆,K.,斯威特,R.M.,布洛克,T.和雷明顿,S.J.(1992年)《生物化学》31,9796-9812],而且在催化过程中间接发挥作用。这解释了肽和酯底物水解的pH行为,此外,L-氨基酸酰胺在氨解反应中比L-氨基酸是更好的亲核试剂。