DOI QR코드

DOI QR Code

α-Glucosidase inhibitory activity and protease characteristics produced by Bacillus amyloliquefaciens

Bacillus amyloliquefaciens로부터 생산된 protease 특성 및 α-glucosidase 저해활성

  • Lee, Rea-Hyun (Department of Food Science and Technology, Catholic University of Daegu) ;
  • Yang, Su-Jin (Department of Food Science and Technology, Catholic University of Daegu) ;
  • Hwang, Tae-Young (Department of Food Science and Technology, Jungwon University) ;
  • Chung, Shin-Kyo (School of Food Science and Biotechnology, Kyungpook National University) ;
  • Hong, Joo-Heon (Department of Food Science and Technology, Catholic University of Daegu)
  • 이래현 (대구가톨릭대학교 식품공학전공) ;
  • 양수진 (대구가톨릭대학교 식품공학전공) ;
  • 황태영 (중원대학교 식품공학과) ;
  • 정신교 (경북대학교 식품공학부) ;
  • 홍주헌 (대구가톨릭대학교 식품공학전공)
  • Received : 2015.07.27
  • Accepted : 2015.10.07
  • Published : 2015.10.30

Abstract

In this study, three GRAS (generally recognized as safety) strain was isolated from Doenjang and Cheonggukjang and identified as a protease-producing microorganism, following the appearance of a clear zone around its colony when cultured on a medium containing skim milk. Based on an analysis of the nucleotide sequence of 16S ribosomal RNA, the strains wereas identified as Bacillus amyloliquefaciens and wereas therefore named Bacillus amyloliquefaciens CDD5, Bacillus amyloliquefaciens CPD4, and Bacillus amyloliquefaciens CGD3. Here, we analyzed the protease and ${\alpha}$-glucosidase inhibitory activities of the three B. amyloliquefaciens strains. Among the isolated strains, B. amyloliquefaciens CGD3 exhibited the highest protease activity (9.21 U/mL, 24 hr). The protease activities of B. amyloliquefaciens CDD5 and B. amyloliquefaciens CPD4 reached 1.14 U/mL and 8.02 U/mL, respectively, at 48 hr. The proteases from the three B. amyloliquefaciens strains showed the highest activities within a pH range of 8.0-9.0 at $50^{\circ}C$, and casein was found to be the preferred substrate on evaluating enzyme activity in the substrate specificity assay. The B. amyloliquefaciens strains exhibited maximal growth when the nutrient broth medium had an initial pH within the range of 5.0-10.0, 6-9% sodium chloride (NaCl), and 5% glucose. B. amyloliquefaciens CDD5 exhibited a low ${\alpha}$-glucosidase inhibition rate (5.32%), whereas B. amyloliquefaciens CPD4 and B. amyloliquefaciens CGD3 exhibited relatively higher inhibition rates of 96.89% and 97.55%, respectively.

본 연구에서는 새로운 프로바이오틱스를 선발하고자 protease를 생산하는 GRAS균주를 된장 및 청국장으로부터 분리하고 그 특성을 조사하였다. 분리한 균주를 분리 동정한 결과 각각 B. amyloliquefaciens CDD5, B. amyloliquefaciens CPD4 및 B. amyloliquefaciens CGD3로 명명하였다. 분리균주의 생육은 12시간 배양 시, 7.13~7.32 log CFU/mL로 최대 생육도를 보였으며 24시간까지 유지되다가 감소하는 경향을 나타내었고, 그 중 B. amyloliquefaciens CGD3의 protease 활성이 9.21 U/mL로서 가장 높게 나타났다. B. amyloliquefaciens이 생산하는 protease 활성은 pH 7.0~10.0, 온도는 $50^{\circ}C$에서 최적활성을 나타내었으며, casein에서 protease활성이 가장 우수하게 나타났다. pH, NaCl, glucose 농도를 달리한 배양조건에 따른 B. amyloliquefaciens의 생육특성으로는 pH 5.0~10.0의 넓은 범위에서 생육하였고, NaCl은 12% 농도까지 증식하였으며 glucose 5%까지는 생육하나 10% 농도부터는 현저하게 생육이 낮아짐을 확인하였다. 또한 혈당저하를 유도하는 ${\alpha}$-glucosidase의 저해활성을 측정한 결과, B. amyloliquefaciens CPD4 및 B. amyloliquefaciens CGD3에서는 각각 96.65% 및 97.85%의 저해율을 나타내었다. 이러한 결과는 특히 protease활성이 가장 우수하고 ${\alpha}$-glucosidase 또한 높은 저해활성을 가진 B. amyloliquefaciens CGD3 균주의 생육특성을 고려하여 단백질 분해 분야의 프로바이오틱 적용 및 당뇨예방용 기능성식품 소재로의 가능성이 기대된다.

Keywords

References

  1. FAO/WHO (2002) Joint FAO/WHO (Food and Agriculture Organization/ World Healthb Organization) working group report on drafting guidelines for the evaluation of probiotics in food. London, Ontatiio, Canada
  2. Homma N (1998) Bifidobacteria as a resistance factor in human beings. Biosci Microflora, 7, 35-43
  3. Shin HJ, Bang JH, Choi HJ, Kim DW, Ahn CS, Jeong YK, Joo WH (2012) Probiotic potential of indigenous Bacillus sp. BCNU 9028 isolated from Meju. Korean J Food Sci Technol, 22, 605-612
  4. Hairul Islam VI, Prakash Babu N, Pandikumar P, Ignacimuthu S (2011) Isolation and characterization of putative probiotic bacterial strain, Bacillus amyloliquefaciens, from North East Himalayan soil based on in vitro and in vivo functional properties. Probiotics Antimicrob Proteins, 3, 175-185 https://doi.org/10.1007/s12602-011-9081-8
  5. Gupta R, Beg QK, Khan S, Chauhan B (2002) An overview on fermentation, downstream processing and properties of microbial alkaline proteases. Appl Microbiol Biotechnol, 60, 381-395 https://doi.org/10.1007/s00253-002-1142-1
  6. Bae YE, Yoon KH (2012) Production and characterization of thermostable protease from Bacillus licheniformis isolated from Korean traditional soybean paste. Korean J Microbiol, 48, 298-304 https://doi.org/10.7845/kjm.2012.048
  7. Park CS, Min DK, Ahn YS, Lee JH, Hong SK, Kim JH, Kang DK (2002) Isolation and characteristics of soy protein-degrading strain, Bacillus subtilis EB464. J Microbiol Biotechnol, 30, 210-215
  8. Ahn YS, Kim YS, Shin DH (2006) Isolation, identification and fermentation characteristics of Bacillus sp. with high protease activity from traditional Cheonggukjang. Korean J Food Sci Technol, 38, 82-87
  9. Jung HK, Jeong YS, Youn KS, Kim DI, Hong JH (2009) Quality characteristics of soybean paste (Doejang) prepared with Bacillus subtilis DH3 expressing high protease levels and deep-sea water. Korean J Food Preserv, 16, 348-354
  10. Kim DY, Lee ET, Kim SD (2003) Purification and characterization of fibrinolytic enzyme produced by Bacillus subtilis K7 isolated from Korean traditional soy sauce. J Korean Soc Agric Biol Chem, 46, 176-182
  11. Yang SJ, Lee DH, Park HM, Jung HK, Park CS, Hong JH (2014) Amylase activity and characterization of Bacillus subtillis CBD2 isolated from Doenjang. Korean J Food Preserv, 21, 286-293 https://doi.org/10.11002/kjfp.2014.21.2.286
  12. Bell DS (2004) Type 2 diabets melitus : what is the optimal treatment regimen? Am J Med, 116, 23-29 https://doi.org/10.1016/j.amjmed.2003.10.017
  13. Lebovitiz HE (1997) Alpha-glucosidase inhibitors. Endocrinol Metab Clin North Am, 26, 539-551 https://doi.org/10.1016/S0889-8529(05)70266-8
  14. De Melo EB, da Silveira Gomes A, Cavalho I (2006) ${\alpha}$- and ${\beta}$-glucosidase inhibitors : chemical structure and biological activity. Tetrahedron 62, 10277-10302 https://doi.org/10.1016/j.tet.2006.08.055
  15. Courageot MP, Frenkiel MP, Dos Santos CD, Deubel V, Depres P (2000) Alpha-glucosidase inhibitors reduce dengue virus production by affecting the initial steps of virion morphogenesis in the endoplasmic reticulum. J Virol, 74, 564-572 https://doi.org/10.1128/JVI.74.1.564-572.2000
  16. Kim SD (2014) Isolation and characterization of ${\alpha}$ -glucosidase inhibitor produced by Bacillus sp. SKU31-1 Strain. Korean J Microbiol, 50, 381-383 https://doi.org/10.7845/kjm.2014.4081
  17. Schmidit DD, Frommer w, Junge B, Muller L, Wingender W, Truscheit E, Schafer D (1977) Alpha-glucosidase inhibitors. Naturwissenschaften, 64, 535-536 https://doi.org/10.1007/BF00483561
  18. Zhu YP, Yin LJ, Cheng YQ, Yamaki K, Yutaka M, Su YC, Li LT (2008) Effect of source of carbon and nitrogen on production of ${\alpha}$-glucosidase inhibitor by a newly isolated srain of Bacillus subtillis B2. Food Chem, 109, 737-742 https://doi.org/10.1016/j.foodchem.2008.01.006
  19. Myoung KS, Heo G, Yoon SY, Shim JJ, Lee JH, Lim KS, Huh CS (2008) Inhibitory effect of Bacillus subtillis Y3-7 culture broth on ${\alpha}$-glucosidase activity. Korean J Food Sci Techol, 40, 558-561
  20. Kunitz M (1947) Crystalline soybean trypsin inhibitor. J Gen Physiol, 30, 291-295 https://doi.org/10.1085/jgp.30.4.291
  21. Watanabe J, Kawabata J, Kurihara H, Niki R (1997) Isolation and identification of alpha-glucosidase inhibitors from tochu-cha (Eucommia ulmoides). Biosci Biotech Biochem, 61, 177-178 https://doi.org/10.1271/bbb.61.177
  22. Jung HJ (2012) Preparation of functional deonjang using Bacillus amyloliquefacie -ns isolated from traditional commercial deonjang. MS Thesis. Kyung hee University. Korea. p 16
  23. Lee NR, Go TH, Lee SM, Hong CO, Park KM, Park GT, Hwang DY, Son HJ (2013) Characteristics of Chungkookjang prepared by Bacillus amyloliquefaciens with different soybeans and fermentation temperatures. J Microbiol, 49, 71-77
  24. Lim SI, Kim HK, Yoo JY (2000) Characteristics of protease produced by Bacillus subtillis PCA 20-3 isolated from Korean traditional Meju. Korean J Food Sci Techol, 32, 154-160
  25. Kim JY (2007) Isolation and characterization of an alkaline protease produced by Bacillus subtilis JK-1. J Microbiol, 43, 331-336
  26. Hwang SY (1995) Purification and characterization of extracellular serine protease produced from Bacillus sp. KUN-17. J Korean Soc Appl Biol Chem, 23, 53
  27. Moon SY, Oh TK, Rho HM (1994) Purification and characterization of an extra cellular alkaline protease from Bacillus subtilis RM 615. Korean Biochem J, 27, 323-329
  28. Kim TH, Park SH, Lee DS, Kwon TK, Kim JH, Hong SD (1990) Properties of alkaline protease produced by an alkalophilic Bacillus sp. J Microbiol Biotechnol, 18, 159-163
  29. Bang SH, Jeong IS (2011) Characterization of an alkaline protease from an alkalophilic Bacillus peseudofirmus HS-54. Korean J Microbiol, 47, 194-199
  30. Lim SI, Kwak EJ, Choi SY, Yoo JY (2002) Characteristics of protease produced by Rhizopus stolonifer, Rhizopus oryzae and Absidia corymbifera from Korean traditional Meju. J Korean Soc Food Sci Nutr, 31, 211-215 https://doi.org/10.3746/jkfn.2002.31.2.211
  31. Byun YG, Kim SH, Joo HK, Lee GS, Yim MH (1998) Purification and characterization of protease produced by Bacillus subtilis YG-95. J Korean Soc Appl Biol Chem, 41, 349-354
  32. Bae HC, Choi SH, Na SH, Nam MS (2012) Characteristics of ${\alpha}$-amylase and protease produced from Bacillus amyloliquefacies CNL-90 isolated from malt grain. J Anim Sci Technol, 54, 133-139 https://doi.org/10.5187/JAST.2012.54.2.133
  33. Lee JY, Jeong SJ, Cho MJ, Cho KM, Kim GM, Shin JH, Lee KC, Kim JS, Kim JH (2014) Fibrinolytic activities of Bacillus species isolated from traditional fermented soyfoods. J Agric Life Sci, 48, 163-173 https://doi.org/10.14397/jals.2014.48.2.163
  34. Kim JW (2009) Screening of ${\alpha}$-glucosidase inhibitor producing Bacillus subtillis and its application. MS Thesis. Kangwon University, Korea, p 40-43
  35. Kim SH, Lee JY, Whang GY, Cho YS, Park YS, Kang KD, Seong SI (2011) Isolation and identification of a Bacillus sp. producing ${\alpha}$-glucosidase inhibitor 1-deoxynojirimycin. J Microbiol Biotechnol, 39, 49-55

Cited by

  1. Isolation and Characterization of Protease Producing B. amyloliquefaciens JH-35 from Food Waste vol.35, pp.4, 2016, https://doi.org/10.5338/KJEA.2016.35.4.40