锗(IV)葡萄糖酸配合物对延迟青霉和绿绿青霉α- l -鼠李糖苷酶的影响

Q4 Biochemistry, Genetics and Molecular Biology
O. Gudzenko, N. Borzova, L. Varbanets, I. Seifullina, О.E. Martsinko, О.A. Chebanenko
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引用次数: 0

摘要

α- l -鼠李糖苷酶(α-L-rhamnoside-rhamnohydrolase EC 3.2.1.40)对末端α-1,2-、α-1,4-和α-1,6链鼠李糖残基具有特异性,通常存在于糖缀合物和合成糖苷中,可成功地用于生物技术中水解某些生物类黄酮、糖蛋白、糖脂和其他糖缀合物中的鼠李糖吡喃苷残基。在此之前,我们已经证明了相当一部分的金属配位化合物作为α- l -鼠李糖苷酶活性的效应物。本文研究了新合成的Ge(IV)和Ba(II)、Co(II)、Ni(II)、Cu(II)、Zn(II)与葡萄糖酸配合物对延迟青霉和绿绿青霉α- l -鼠李糖苷酶活性的影响。方法。研究对象为延迟青霉和绿绿正青霉α- l -鼠李糖苷酶。以柚皮苷为底物,采用Davis法测定α- l -鼠李糖苷酶活性。以葡萄糖酸配位物Ge(IV)和Ba(II)、Co(II)、Ni(II)、Cu(II)和Zn(II)作为酶活性调节剂。合成的配合物对应于[М(H2O)6][Ge2(OH)2(C6H8O7)2]·nH2O (М = Ba(1), n=2;有限公司(2),n = 4;倪(3),n = 4;铜(4)、n = 4;锌(5)、n = 3)。结果。研究了配位化合物1-(5)对两株延迟青霉和绿绿青霉α- l -鼠李糖苷酶活性的影响,影响因素随作用时间和浓度的变化而变化。结果表明,化合物(3)在浓度为0.01%(孵育1 h)时,可使tardum α- l -鼠李糖苷酶活性略有提高(5%)。化合物1在浓度为0.1%的条件下,在第一个小时内使tardum α- l -鼠李糖苷酶活性降低29%,孵育24 h后,抑制作用降低15%。化合物2和(4)在暴露1h时激活酶9-39%。在浓度为0.1%、暴露时间为1 h时,化合物1可使紫芥α- l -鼠李糖苷酶活性提高80%,而在浓度降低至0.01%时,活性仅提高29%。一般来说,应该注意的是,在大多数情况下,孵育时间延长至24小时,会导致激活(或抑制)水平下降,并使酶活性恢复到控制值。结论。金属配位化合物对酶活性的各种影响,取决于阳离子的性质和酶的来源,已经确定。与其他金属相比,Ba(II)的参与对红芥α- l -鼠李糖苷酶活性的激活作用最大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Germanium (IV) Complexes with Gluconic Acid as Effectors of Penicillium tardum and Eupenicillium erubescens α-L-Rhamnosidases
α-L-Rhamnosidase (α-L-rhamnoside-rhamnohydrolase EC 3.2.1.40) showing specificity for terminal α-1,2-, α-1,4- and α-1,6-linked rhamnose residues, which often present in glycoconjugates and synthetic glycosides, can be successfully used in biotechnology for the hydrolysis of rhamnopyranoside residues present in some bioflavonoids, glycoproteins, glycolipids, and other glycoconjugates. Previously, we have shown that a significant part of the coordination compounds of various metals act as effectors of the activity of α-L-rhamnosidases. The aim of this investigation was to study the effect of a number of newly synthesized coordination compounds of Ge(IV) and Ba(II), (Co(II), Ni(II), Cu(II), Zn(II) with gluconic acid on the activity of Penicillium tardum and Eupenicillium erubescens α-L-rhamnosidases. Methods. The objects of the study were Penicillium tardum and Eupenicillium erubescens α-L-rhamnosidases. α-L-Rhamnosidase activity was determined by the Davis method using naringin as a substrate. Coordination compounds Ge(IV) and Ba(II), Co(II), Ni(II), Cu(II) ,and Zn(II) with gluconic acid were used as enzyme activity modifiers. The synthesized complexes correspond to the formulas [М(H2O)6][Ge2(OH)2(C6H8O7)2]·nH2O (М = Ba(1), n=2; Co(2), n=4; Ni(3), n=4; Cu(4), n=4; Zn(5), n=3). Results. The effect of coordination compounds 1-(5) on the activity of α-L-rhamnosidase in two strains of Penicillium tardum and Eupenicillium erubescens was studied depending on the exposure time and concentration of the effector. It was shown that compound (3) at a concentration of 0.01% (1 h incubation) led to a slight (by 5%) increase in the activity of P. tardum α-L-rhamnosidase. Compound 1 at a concentration of 0.1% led to a decrease in the activity of P. tardum α-L-rhamnosidase by 29% during the first hour, and after 24 h of incubation, a decrease in the inhibitory effect to 15% was noted. Compounds 2 and (4) activated the enzyme by 9-39% at 1h exposure. At a concentration of 0.1% and exposure time of 1 h, compound 1 increased the activity of E. erubescens α-L-rhamnosidase by 80%, while at a decrease in concentration to 0.01%, the activity increased only by 29%. In general, it should be noted that in most cases, an increase in the duration of incubation up to 24 h led to a decrease in the level of activation (or inhibition) and a return to the control values of enzyme activity. Conclusions. The variety of effects of metal coordination compounds on the activity of enzymes, depending on the nature of the cation and the origin of the enzyme, has been established. The involvement of Ba(II) had the greatest activating effect on the activity of E. erubescens α-L-rhamnosidase compared to other metals.
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Mikrobiolohichnyi zhurnal
Mikrobiolohichnyi zhurnal Medicine-Microbiology (medical)
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