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http://dx.doi.org/10.4014/mbl.1912.12004

Properties of β-Galactosidase from Lactobacillus zymae GU240, an Isolate from Kimchi, and Its Gene Cloning  

Le, Huong Giang (Division of Applied Life Science (BK21 Plus), Graduate School, Gyeongsang National University)
Yao, Zhuang (Division of Applied Life Science (BK21 Plus), Graduate School, Gyeongsang National University)
Kim, Jeong A (Institute of Agriculture and Life Science, Gyeongsang National University)
Lee, Se Jin (Division of Applied Life Science (BK21 Plus), Graduate School, Gyeongsang National University)
Meng, Yu (Division of Applied Life Science (BK21 Plus), Graduate School, Gyeongsang National University)
Park, Ji Yeong (Division of Applied Life Science (BK21 Plus), Graduate School, Gyeongsang National University)
Kim, Jeong Hwan (Division of Applied Life Science (BK21 Plus), Graduate School, Gyeongsang National University)
Publication Information
Microbiology and Biotechnology Letters / v.48, no.3, 2020 , pp. 287-295 More about this Journal
Abstract
Lactobacillus zymae GU240 was previously isolated from Kimchi, a Korean fermented vegetable, as a strong GABA producer. The strain showed β-galactosidase (β-Gal) activity on MRS agar plates with X-gal. When growth and β-Gal activities of GU240 were measured using MRS (glucose, 2%, w/v) and MRSL (lactose, 2%, w/v) broths, cells were found to grow slowly in MRSL, and the β-Gal activity (36 units at 4 h) was lower than that of cells grown in MRS (94 units at 16 h). The highest OD600 value of the culture in MRS was 1.6 at 24 h at 37℃, whereas that of the culture in MRSL was 0.6 at 16 h. β-Gal activity of the culture in MRS reached the maximum (95.6 u/ml) at 16 h, decreased thereafter, and was not detected at 48 h. β-Gal activity for culture in MRSL reached its highest (36 u/ml) at 4 h and decreased gradually, but some activity (11.05 u/ml) still remained at 72 h. The structural gene encoding β-Gal in L. zymae GU240 was cloned as a 3.1 kb fragment, and DNA sequencing confirmed the presence of complete lacLM genes. lacLM genes from L. zymae GU240 showed 98-99% homologies in nucleotide sequences with other lacLM genes from L. brevis. Reverse transcription (RT)-PCR confirmed the operon structure of lacLM. The results indicated that L. zymae GU240 might be in the process of losing the ability to grow rapidly on lactose-containing medium, such as milk, due to adaptations to plant environments, including kimchi.
Keywords
Lactobacillus zymae GU240; ${\beta}$-galactosidase; lacLM; Kimchi;
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1 Juers DH, Matthews BW, Huber RE. 2012. LacZ ${\beta}$-galactosidase: structure and function of an enzyme of historical and molecular biological importance. Protein Sci. 21: 1792-1807.   DOI
2 De Vos WM, Vaughan EE. 1994. Genetics of lactose utilization in lactic acid bacteria. FEMS Microbiol. Rev. 15: 217-237.   DOI
3 De Vos WM, Simons G. 1988. Molecular cloning of lactose genes in dairy lactic streptococci: the phospho-${\beta}$-galactosidase and ${\beta}$-galactosidase genes and their expression products. Biochimie 70: 461-473.   DOI
4 Vaughan EE, Pridmore RD, Mollet B. 1998. Transcriptional regulation and evolution of lactose genes in the galactose-lactose operon of Lactococcus lactis NCDO2054. J. Bacteriol. 180: 4893-4902.   DOI
5 Nguyen TH, Splechtna B, Yamabhai M, Haltrich D, Peterbauer C. 2007. Cloning and expression of the ${\beta}$-galactosidase genes from Lactobacillus reuteri in Escherichia coli. J. Biotechnol. 129: 581-591.   DOI
6 Obst M, Meding ER, Vogel RF, Hammes WP. 1995. Two genes encoding the ${\beta}$-galactosidase of Lactobacillus sake. Microbiology 141: 3059-3066.   DOI
7 Adams RM, Yoast S, Mainzer SE, Moon K, Palombella AL, Estell DA. et al. 1994. Characterization of two cold-sensitive mutants of the ${\beta}$-galactosidase from Lactobacillus delbruckii subsp. bulgaricus. J. Biol. Chem. 269: 5666-5672.   DOI
8 Franco D, de Boer PA, de Gier-de Vries C, Lamers WH, Mooman AF. 2001. Methods on in situ hybridization, immunohistochemistry and beta-galactosidase reporter gene detection. Eur. J. Morphol. 39: 3-25.   DOI
9 Oliveira C, Guimaraes PMR, Domingues L. 2011. Recombinant microbial systems for improved ${\beta}$-galactosidase production and biochemical applications. Biotechnol. Adv. 29: 600-609.   DOI
10 Platteeuw C, van Allen-Boerrigter I, van Schalkwijk S, de Vos EM. 1996. Food-grade cloning and expression system for Lactococcus lactis. Appl. Environ. Microbiol. 62: 1008-1013.   DOI
11 Landete JM. 2017. A review of food-grade vectors in lactic acid bacteria: from the laboratory to their application. Crit. Rev. Biotechnol. 37: 296-308.   DOI
12 Park JY, Jeong SJ, Kim JH. 2014. Characterization of a glutamate decarboxylase (GAD) gene from Lactobacillus zymae. Biotechnol. Lett. 36: 1791-1799.   DOI
13 Miller JH. 1972. Experiments in molecular genetics, Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
14 Park RJ, Lee KW, Kim SJ, Park JY, Nam SJ, Park JY, et al. 2002. Isolation of Lactococcus lactis strain with ${\beta}$-galactosidase activity from Kimchi and cloning of lacZ gene from the isolated strain. J. Microbiol. Biotechnol. 12: 157-161.
15 Heo K, Cho KM, Lee CK, Kim GM, Shin JH, Kim JS, et al. 2013. Characterization of a fibrinolytic enzyme secreted by Bacillus amyloliquefaciens CB1 and its gene cloning. J. Microbiol. Biotechnol. 23: 974-983.   DOI
16 Sa HD, Park JY, Jeong SJ, Lee KW, Kim JH. 2015. Characterization of glutamate decarboxylase (GAD) from Lactobacillus sakei A156 isolated from Jeot-gal. J. Microbiol. Biotechnol. 25: 696-703.   DOI
17 Saier MH, Chauvaux S, Cook GM, Deutscher J, Paulsen IT, Reizer J, et al. 1996. Catabolite repression and inducer control in Grampositive bacteria. Microbiology 142: 217-223.   DOI
18 Kim TY, Lee JM, Chang HC, Chung DK, Lee JH, Kim JH, et al. 1999. Effect of temperature and a carbon source on the expression of ${\beta}$-galactosidase gene of Lactococcus lactis spp. lactis ATCC7962. J. Microbiol. Biotechnol. 9: 201-205.
19 David S, Stevens H, van Riel M, Sinons G, de Vos W. 1992. Leuconostoc lactis ${\beta}$-galactosidase is encoded by two overlapping genes. J. Bacteriol. 174: 4475-4481.   DOI
20 Chanalia P, Gandhi D, Attri P, Dhanda S. 2018. Purification and characterization of ${\beta}$-galactosidase from probiotic Pediococcus acidilactici and its use in milk lactose hydrolysis and galactooligosaccharide synthesis. Bioorg. Chem. 77: 176-189.   DOI