Exterkate F A, Alting A C, Slangen C J
Netherlands Institute for Dairy Research (NIZO), Ede.
Biochem J. 1991 Jan 1;273(Pt 1)(Pt 1):135-9. doi: 10.1042/bj2730135.
The specificity of two genetically related cell-envelope serine proteinases (PI-type and PIII-type) of Lactococcus lactis subsp. cremoris towards the alpha s1-casein-(1-23)-fragment, an important intermediate product of primary chymosin-directed proteolysis in cheese, has been established. Both enzymes showed, at pH 6.5 and under relatively low-ionic-strength conditions, a characteristic, mutually different, cleavage pattern that seems, in the first instance, to be determined by the charge N-terminal to the cleaved bond. With Pi, three cleavage sites were found in the N-terminal positively charged part of the peptide and, with PIII, three sites were found in the C-terminal negatively charged part. Comparison of the specific cleavage sites in this peptide and those in beta-casein revealed similarities with respect to the different residues which can occur N-terminally to the cleaved bond. The properties of these substrate residues match with the structural and various interactive features of the respective binding regions of the enzymes predicted on the basis of a close sequence similarity of the lactococcal proteinases with the subtilisin family. A hydrophobic interaction and/or hydrogen-bridge formation seems to govern the binding of the first amino acid residue N-terminal to the scissile bond. The more distantly N-terminally positioned sequence of residues apparently is attracted electrostatically by a negative charge in the binding region of PI and by a positive charge in that of PIII, provided that the opposite charge is is present at the appropriate position in this sequence. Hence a specific electrostatic binding may occur; additionally, hydrophobic interaction and/or hydrogen-bond formation is important.
乳酸乳球菌乳脂亚种的两种基因相关的细胞包膜丝氨酸蛋白酶(PI型和PIII型)对αs1-酪蛋白-(1-23)片段(奶酪中凝乳酶直接蛋白水解的重要中间产物)的特异性已经确定。在pH 6.5和相对低离子强度条件下,这两种酶都显示出一种特征性的、彼此不同的切割模式,乍一看,这种模式似乎首先由切割键N端的电荷决定。对于PI,在肽的N端带正电荷部分发现了三个切割位点,对于PIII,在C端带负电荷部分发现了三个位点。该肽中的特定切割位点与β-酪蛋白中的切割位点的比较揭示了在切割键N端可能出现的不同残基方面的相似性。这些底物残基的特性与基于乳球菌蛋白酶与枯草杆菌蛋白酶家族的紧密序列相似性预测的酶各自结合区域的结构和各种相互作用特征相匹配。疏水相互作用和/或氢键形成似乎控制着切割键N端第一个氨基酸残基的结合。残基序列中位置较远的N端部分显然被PI结合区域中的负电荷和PIII结合区域中的正电荷静电吸引,前提是该序列中适当位置存在相反电荷。因此可能发生特异性静电结合;此外,疏水相互作用和/或氢键形成也很重要。