AN ACTIVE-SITE PEPTIDE-CONTAINING THE 2ND ESSENTIAL CARBOXYL GROUP OF DEXTRANSUCRASE FROM LEUCONOSTOC-MESENTEROIDES BY CHEMICAL MODIFICATIONS
AN ACTIVE-SITE PEPTIDE-CONTAINING THE 2ND ESSENTIAL CARBOXYL GROUP OF DEXTRANSUCRASE FROM LEUCONOSTOC-MESENTEROIDES BY CHEMICAL MODIFICATIONS
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DOI：
10.1021/bi00212a039
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发表时间：
1993-12-14
期刊：
影响因子：
2.9
通讯作者：
KOBAYASHI, M
中科院分区：
文献类型：
--
作者：
FUNANE, K;SHIRAIWA, M;KOBAYASHI, M
The treatment of Leuconostoc mesenteroides B-512F dextransucrase with 10 mM 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide (EDC) and glycine ethyl ester (GEE) inactivated the enzyme almost completely within 24 min where the modification of one carboxyl group/mol of the enzyme by EDC was attained. Though 30 mM diethyl pyrocarbonate (DEP) also inactivated the enzyme, about 35% of the activity remained during a 36-min incubation. When 10 mol of imidazole residues/mol of the enzyme was modified by DEP, 50% of the activity was still retained. The addition of the substrate sucrose greatly retarded the enzyme inactivation by EDC. However, the addition of dextran slightly protected the inactivation of the glucosyl-transferring activity and accelerated the inactivation of the sucrose-cleaving activity. In the case of DEP, the addition of sucrose or dextran gave no influence on the inactivation of the enzyme. Therefore, the carboxyl group seemed to play a more important role in the substrate binding and in the catalytic activity of the dextransucrase than the imidazolium group. Differential labeling of Leuconostoc dextransucrase by EDC was conducted in the presence of a sucrose analog, sucrose monocaprate. The fluorescent probe N-(1-naphthyl)ethylenediamine (EDAN) was used as the nucleophile instead of GEE. A fluorescent labeled peptide was isolated from a trypsin digest of the EDC-EDAN modified enzyme. The amino acid sequence of the isolated peptide was Leu-Gln-Glu-Asp-Asn-Ser-Asn-Val-Val-Val-Glu-Ala. The sequence had about 58% homology to those of streptococcal glucosyltransferases GTF-S and GTF-I producing soluble and insoluble dextrans. Those peptides were distinguished from the active-site peptides of GTF-S and GTF-I from S. mutans, which contained catalytic aspartic acid residues of Asp465 and Asp451, respectively. They were located at 30-45 amino acids toward the amino terminal from the catalytic aspartic acid. Therefore, the isolated peptide seemed to contain the second essential carboxyl group for the catalytic activity.
