Biochemical characterization of a novel cycloisomaltooligosaccharide glucanotransferase from Paenibacillus sp. 598K

Cycloisomaltooligosaccharide glucanotransferase (CITase; EC 2.4.1.248), a member of the glycoside hydrolase family 66 (GH66), catalyzes the intramolecular transglucosylation of dextran to produce cycloisomaltooligosaccharides (CIs; cyclodextrans) of varying lengths. Eight CI-producing bacteria have...

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Veröffentlicht in:Biochimica et biophysica acta 2012-07, Vol.1824 (7), p.919-924
Hauptverfasser: Suzuki, Ryuichiro, Terasawa, Kazue, Kimura, Keitarou, Fujimoto, Zui, Momma, Mitsuru, Kobayashi, Mikihiko, Kimura, Atsuo, Funane, Kazumi
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Sprache:eng
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Zusammenfassung:Cycloisomaltooligosaccharide glucanotransferase (CITase; EC 2.4.1.248), a member of the glycoside hydrolase family 66 (GH66), catalyzes the intramolecular transglucosylation of dextran to produce cycloisomaltooligosaccharides (CIs; cyclodextrans) of varying lengths. Eight CI-producing bacteria have been found; however, CITase from Bacillus circulans T-3040 (CITase-T3040) is the only CI-producing enzyme that has been characterized to date. In this study, we report the gene cloning, enzyme characterization, and analysis of essential Asp and Glu residues of a novel CITase from Paenibacillus sp. 598K (CITase-598K). The cit genes from T-3040 and 598K strains were expressed recombinantly, and the properties of Escherichia coli recombinant enzymes were compared. The two CITases exhibited high primary amino acid sequence identity (67%). The major product of CITase-598K was cycloisomaltoheptaose (CI-7), whereas that of CITase-T3040 was cycloisomaltooctaose (CI-8). Some of the properties of CITase-598K are more favorable for practical use compared with CITase-T3040, i.e., the thermal stability for CITase-598K (≤50°C) was 10°C higher than that for CITase-T3040 (≤40°C); the kcat/KM value of CITase-598K was approximately two times higher (32.2s−1mM−1) than that of CITase-T3040 (17.8s−1mM−1). Isomaltotetraose was the smallest substrate for both CITases. When isomaltoheptaose or smaller substrates were used, a lag time was observed before the intramolecular transglucosylation reaction began. As substrate length increased, the lag time shortened. Catalytically important residues of CITase-598K were predicted to be Asp144, Asp269, and Glu341. These findings will serve as a basis for understanding the reaction mechanism and substrate recognition of GH66 enzymes. [Display omitted] ► CITse-598K is a novel cycloisomaltooligosaccharide glucanotransferase. ► CITase-598K exhibited higher activity and thermal stability. ► The major product of CITase-598K was cycloisomaltoheptaose. ► The minimum size of substrate for CITase is isomaltotetraose. ► Asp144, Asp269, and Glu341 of CITase-598K are catalytically important.
ISSN:1570-9639
0006-3002
1878-1454
DOI:10.1016/j.bbapap.2012.04.001