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PMID: 10825529 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Structure, specificity and function of cyclomaltodextrinase, a multispecific enzyme of the alpha-amylase family.

Biochimica et biophysica acta ·Vol. 1478 ·No. 2 ·2000-05-23 ·Pages 165-85

Park KH, Kim TJ, Cheong TK, Kim JW, Oh BH, Svensson B

Abstract

Cyclomaltodextrinase (CDase, EC 3.2.1.54), maltogenic amylase (EC 3. 2.1.133), and neopullulanase (EC 3.2.1.135) are reported to be capable of hydrolyzing all or two of the following three types of substrates: cyclomaltodextrins (CDs); pullulan; and starch. These enzymes hydrolyze CDs and starch to maltose and pullulan to panose by cleavage of alpha-1,4 glycosidic bonds whereas alpha-amylases essentially lack activity on CDs and pullulan. They also catalyze transglycosylation of oligosaccharides to the C3-, C4- or C6-hydroxyl groups of various acceptor sugar molecules. The present review surveys the biochemical, enzymatic, and structural properties of three types of such enzymes as defined based on the substrate specificity toward the CDs: type I, cyclomaltodextrinase and maltogenic amylase that hydrolyze CDs much faster than pullulan and starch; type II, Thermoactinomyces vulgaris amylase II (TVA II) that hydrolyzes CDs much less efficiently than pullulan; and type III, neopullulanase that hydrolyzes pullulan efficiently, but remains to be reported to hydrolyze CDs. These three types of enzymes exhibit 40-60% amino acid sequence identity. They occur in the cytoplasm of bacteria and have molecular masses from 62 to 90 kDa which are slightly larger than those of most alpha-amylases. Multiple amino acid sequence alignment and crystal structures of maltogenic amylase and TVA II reveal the presence of an N-terminal extension of approximately 130 residues not found in alpha-amylases. This unique N-terminal domain as seen in the crystal structures apparently contributes to the active site structure leading to the distinct substrate specificity through a dimer formation. In aqueous solution, most of these enzymes show a monomer-dimer equilibrium. The present review discusses the multiple specificity in the light of the oligomerization and the molecular structures arriving at a clarified enzyme classification. Finally, a physiological role of the enzymes is proposed.

MeSH Terms
Amino Acid Sequence Binding Sites Conserved Sequence Cyclodextrins/metabolism Glucans/metabolism Glycoside Hydrolases/chemistry,genetics,metabolism Glycosylation Micromonosporaceae Models, Molecular Molecular Sequence Data Protein Conformation Sequence Alignment Starch/metabolism Substrate Specificity
Chemicals
Cyclodextrins Glucans pullulan Starch Glycoside Hydrolases glucan 1,4-alpha-maltohydrolase neopullulanase cyclomaltodextrinase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Park K H
Research Center for New Bio-Materials in Agriculture and Department of Food Science and Technology, Seoul National University, Suwon, South Korea.
Kim T J
Cheong T K
Kim J W
Oh B H
Svensson B
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
2000-05-23
Pages
165-85
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
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