Exterkate F A
Netherlands Institute for Dairy Research (NIZO), Ede.
Appl Microbiol Biotechnol. 1990 Jul;33(4):401-6. doi: 10.1007/BF00176654.
Various chromophoric peptides have been tested as substates for two genetically related types (PI and PIII) of cell-envelope proteinases of Lactococcus lactis subsp. cremoris. The positively charged peptide methoxy-succinyl-arginyl-prolyl-tyrosyl-p-nitroanilide appeared to be cleaved with the highest catalytic efficiency by both enzymes, although in the case of PIII only at high ionic strength. A cation binding site in the PI-type proteinase that is not present in the related PIII-type appears to be mainly responsible for the difference between these enzymes with respect to the rate of conversion of this chromophoric substrate at relatively low ionic strength. This cation binding site most probably resides in the aspartic acid residue 166, which in PIII is substituted by asparagine. Substitution of the threonine residue 138 by lysine in PIII may also play a role. The binding step in the reaction pathway catalysed by PI at low ionic strength is governed mainly by an ionic interaction involving the cation binding site. In addition, hydrophobic interactions contribute to the binding process. Masking of the cation binding site only increases the Michaelis constant Km; the catalytic constant kcat is not affected. In the absence of the cation binding site (viz. in PIII) the free energy derived from the hydrophobic interactions only is too small to promote binding of the substrate effectively. High activities are measured only if a high ionic strength is introduced. Removal of electrostatic repulsion between the substrate and positively charged residues of the enzyme, among which is lysine 138, may contribute to this activation.(ABSTRACT TRUNCATED AT 250 WORDS)
多种发色肽已被测试作为乳酸乳球菌亚种cremoris两种遗传相关类型(PI和PIII)的细胞包膜蛋白酶的底物。带正电荷的肽甲氧基琥珀酰精氨酰脯氨酰酪氨酰对硝基苯胺似乎被这两种酶以最高催化效率切割,不过在PIII的情况下仅在高离子强度下才会如此。PI型蛋白酶中存在而相关的PIII型中不存在的一个阳离子结合位点,似乎是造成这两种酶在相对低离子强度下对这种发色底物转化速率差异的主要原因。这个阳离子结合位点很可能位于天冬氨酸残基166处,在PIII中该残基被天冬酰胺取代。PIII中苏氨酸残基138被赖氨酸取代也可能起作用。PI在低离子强度下催化的反应途径中的结合步骤主要由涉及阳离子结合位点的离子相互作用控制。此外,疏水相互作用也有助于结合过程。掩盖阳离子结合位点只会增加米氏常数Km;催化常数kcat不受影响。在没有阳离子结合位点的情况下(即PIII中),仅由疏水相互作用产生的自由能太小,无法有效促进底物结合。只有引入高离子强度时才能测得高活性。消除底物与酶的带正电荷残基(其中包括赖氨酸138)之间的静电排斥,可能有助于这种激活。(摘要截短于250词)