DOI QR코드

DOI QR Code

Comparison of Catalyzing Properties of Bacterial 4-α-Glucanotransferases Focusing on Their Cyclizing Activity

  • Kim, Jung-Eun (Department of Food Science and Technology, Chungnam National University) ;
  • Tran, Phuong Lan (Department of Food Science and Technology, Chungnam National University) ;
  • Ko, Jae-Min (Department of Food Science and Technology, Chungnam National University) ;
  • Kim, Sa-Rang (Department of Food Nutrition, Chungnam National University) ;
  • Kim, Jae-Han (Department of Food Nutrition, Chungnam National University) ;
  • Park, Jong-Tae (Department of Food Science and Technology, Chungnam National University)
  • Received : 2020.09.10
  • Accepted : 2020.10.06
  • Published : 2021.01.28

Abstract

A newly cloned 4-α-glucanotransferase (αGT) from Deinococcus geothermalis and two typical bacterial αGTs from Thermus scotoductus and Escherichia coli (MalQ) were investigated. Among 4 types of catalysis, the cyclization activity of αGTs that produces cycloamylose (CA), a valuable carbohydrate making inclusion complexes, was intensively studied. The new αGT, DgαGT, showed close protein sequence to the αGT from T. scotoductus (TsαGT). MalQ was clearly separated from the other two αGTs in the phylogenetic and the conserved regions analyses. The reaction velocities of disproportionation, cyclization, coupling, and hydrolysis of three αGTs were determined. Intriguingly, MalQ exhibited more than 100-fold lower cyclization activity than the others. To lesser extent, the disproportionation activity of MalQ was relatively low. DgαGT and TsαGT showed similar kinetics results, but TsαGT had nearly 10-fold lower hydrolysis activity than DgαGT. Due to the very low cyclizing activity of MalQ, DgαGT and TsαGT were selected for further analyses. When amylose was treated with DgαGT or TsαGT, CA with a broad DP range was generated immediately. The DP distribution of CA had a bimodal shape (DP 7 and 27 as peaks) for the both enzymes, but larger DPs of CA quickly decreased in the DgαGT. Cyclomaltopentaose, a rare cyclic sugar, was produced at early reaction stage and accumulated as the reactions went on in the both enzymes, but the increase was more profound in the TsαGT. Taken together, we clearly demonstrated the catalytic differences between αGT groups from thermophilic and pathogenic bacteria that and showed that αGTs play different roles depending on their lifestyle.

Keywords

References

  1. Nguyen DHD, Park S-H, Tran PL, Kim J-W, Le QT, Boos W, et al. 2019. Characterization of the transglycosylation reaction of 4-α-Glucanotransferase (MalQ) and its role in glycogen breakdown in Escherichia coli. J. Microbiol. Biotechnol. 29: 357-366. https://doi.org/10.4014/jmb.1811.11051
  2. Jeong D-W, Jeong H-M, Shin Y-J, Woo S-H, Shim J-H. 2019. Properties of recombinant 4-α-glucanotransferase from Bifidobacterium longum subsp. longum JCM 1217 and its application. Food Sci. Biotechnol. 29: 667-674. https://doi.org/10.1007/s10068-019-00707-4
  3. Takaha T, Smith SM. 1999. The functions of 4-α-glucanotransferases and their use for the production of cyclic glucans. Biotechnol. Genet. Eng. Rev. 16: 257-280. https://doi.org/10.1080/02648725.1999.10647978
  4. Takaha T, Yanase M, Okada S, Smith SM. 1993. Disproportionating enzyme (4-alpha-glucanotransferase; EC 2.4. 1.25) of potato. Purification, molecular cloning, and potential role in starch metabolism. J. Biol. Chem. 268: 1391-1396. https://doi.org/10.1016/S0021-9258(18)54088-6
  5. Park J-H, Kim H-J, Kim Y-H, Cha H, Kim Y-W, Kim T-J, et al. 2007. The action mode of Thermus aquaticus YT-1 4-α-glucanotransferase and its chimeric enzymes introduced with starch-binding domain on amylose and amylopectin. Carbohydr. Polym. 67: 164-173. https://doi.org/10.1016/j.carbpol.2006.05.018
  6. Lee KY, Kim Y-R, Park KH, Lee HG. 2006. Effects of α-glucanotransferase treatment on the thermo-reversibility and freeze-thaw stability of a rice starch gel. Carbohydr. Polym. 63: 347-354. https://doi.org/10.1016/j.carbpol.2005.08.050
  7. Terada Y, Fujii K, Takaha T, Okada S. 1999. Thermus aquaticus ATCC 33923 amylomaltase gene cloning and expression and enzyme characterization: production of cycloamylose. Appl. Environ. Microbiol. 65: 910-915. https://doi.org/10.1128/aem.65.3.910-915.1999
  8. Liebl W, Feil R, Gabelsberger J, Kellermann J, Schleifer KH. 1992. Purification and characterization of a novel thermostable 4-α-glucanotransferase of Thermotoga maritima cloned in Escherichia coli. Eur. J. Biochem. 207: 81-88. https://doi.org/10.1111/j.1432-1033.1992.tb17023.x
  9. Dippel R, Boos W. 2005. The maltodextrin system of Escherichia coli: metabolism and transport. J. Bacteriol. 187: 8322-8331. https://doi.org/10.1128/JB.187.24.8322-8331.2005
  10. Lim MS, Myung Hee Lee, Jeong Huyn Lee, Hyun-Mok Ju, Na Young Park, Hye Sook Jeong, et al. 2005. Identification and characterization of the Vibrio vulnificus malPQ operon. J. Microbiol. Biotechnol. 15: 616-625.
  11. Han A-r, Lee Y-j, Wang T, Kim J-W. 2018. Glycogen metabolism in Vibrio vulnificus affected by malP and malQ. Microbiol. Biotchnol. Lett. 46: 29-39. https://doi.org/10.4014/mbl.1801.01002
  12. Park J-T, Shim J-H, Tran PL, Hong I-H, Yong H-U, Oktavina EF, et al. 2011. Role of maltose enzymes in glycogen synthesis by Escherichia coli. J. Bacteriol. 193: 2517-2526. https://doi.org/10.1128/JB.01238-10
  13. van der Veen BA, van Alebeek GJW, Uitdehaag JC, Dijkstra BW, Dijkhuizen L. 2000. The three transglycosylation reactions catalyzed by cyclodextrin glycosyltransferase from Bacillus circulans (strain 251) proceed via different kinetic mechanisms. Eur. J. Biochem. 267: 658-665. https://doi.org/10.1046/j.1432-1327.2000.01031.x
  14. Tachibana Y, Takaha T, Fujiwara S, Takagi M, Imanaka T. 2000. Acceptor specificity of 4-α-glucanotransferase from Pyrococcus kodakaraensis KOD1, and synthesis of cycloamylose. J. Biosci. Bioeng. 90: 406-409. https://doi.org/10.1016/S1389-1723(01)80009-8
  15. Yanase M, Takata H, Takaha T, Kuriki T, Smith SM, Okada S. 2002. Cyclization reaction catalyzed by glycogen debranching enzyme (EC 2.4. 1.25/EC 3.2. 1.33) and its potential for cycloamylose production. Appl. Environ. Microbiol. 68: 4233-4239. https://doi.org/10.1128/AEM.68.9.4233-4239.2002
  16. Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, et al. 1997. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25: 3389-3402. https://doi.org/10.1093/nar/25.17.3389
  17. Laemmli UK. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680-685. https://doi.org/10.1038/227680a0
  18. Werner W, Rey He, Wielinger H. 1970. Properties of a new chromogen for determination of glucose in blood according to god/podmethod. Z. Anal. Chem. Freseniu. 252: 224. https://doi.org/10.1007/BF00546391
  19. Koizumi K, Sanbe H, Kubota Y, Terada Y, Takaha T. 1999. Isolation and characterization of cyclic α-(1→ 4)-glucans having degrees of polymerization 9-31 and their quantitative analysis by high-performance anion-exchange chromatography with pulsed amperometric detection. J. Chromatogr. A 852: 407-416. https://doi.org/10.1016/S0021-9673(99)00643-3
  20. Fox JD, Robyt JF. 1991. Miniaturization of three carbohydrate analyses using a microsample plate reader. Anal. Biochem. 195: 93-96. https://doi.org/10.1016/0003-2697(91)90300-I
  21. Oh MJ, Hua S, Kim BJ, Jeong HN, Jeong SH, Grimm R, et al. 2013. Analytical platform for glycomic characterization of recombinant erythropoietin biotherapeutics and biosimilars by MS. Bioanalysis 5: 545-559. https://doi.org/10.4155/bio.12.327
  22. Murakami T, Kanai T, Takata H, Kuriki T, Imanaka T. 2006. A novel branching enzyme of the GH-57 family in the hyperthermophilic archaeon Thermococcus kodakaraensis KOD1. J. Bacteriol. 188: 5915-5924. https://doi.org/10.1128/JB.00390-06
  23. Sasaki Y, Nomura Y, Sawada S-i, Akiyoshi K. 2010. Polysaccharide nanogel-cyclodextrin system as an artificial chaperone for in vitro protein synthesis of green fluorescent protein. Polymer J. 42: 823-828. https://doi.org/10.1038/pj.2010.73
  24. Yamaguchi H, Miyazaki M. 2014. Refolding techniques for recovering biologically active recombinant proteins from inclusion bodies. Biomolecules 4: 235-251. https://doi.org/10.3390/biom4010235
  25. Gattuso G, Nepogodiev SA, Stoddart JF. 1998. Synthetic cyclic oligosaccharides. Chem. Rev. 98: 1919-1958. https://doi.org/10.1021/cr960133w
  26. Watanabe H, Nishimoto T, Sonoda T, Kubota M, Chaen H, Fukuda S. 2006. An enzymatically produced novel cyclomaltopentaose cyclized from amylose by an α-(1→ 6)-linkage, cyclo-{→ 6)-α-D-Glcp-(1→ 4)-α-D-Glcp-(1→ 4)-α-D-Glcp-(1→ 4)-α-D-Glcp-(1→ 4)- α-D-Glcp-(1→}. Carbohydr.Res. 341: 957-963. https://doi.org/10.1016/j.carres.2006.02.028