A food-grade expression/secretion vector for Lactococcus lactis that uses an α-galactosidase gene as a selection marker

被引:28
作者
Jeong, DW
Lee, JH
Kim, KH
Lee, HJ [1 ]
机构
[1] Seoul Natl Univ, Sch Agr Biotechnol, Seoul 151742, South Korea
[2] Seoul Natl Univ, Ctr Agr Biomat, Seoul 151742, South Korea
[3] Kyonggi Univ, Dept Food Sci & Biotechnol, Suwon 443760, South Korea
[4] Korea Univ, Coll Life & Environm Sci, Div Food Sci, Seoul 136713, South Korea
关键词
Lactococcus lactis; food-grade expression/secretion vector; alpha-galactosidase; nisA promoter; usp45 signal peptide;
D O I
10.1016/j.fm.2005.06.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A new food-grade expression/secretion vector for lactococci, pFMN30, was developed using an a-galactosidase gene (melA) of Lactobacillus plantarum as a selection marker. The 4.9-kb pFMN30 is a derivative of the lactococcal vector pMG36e containing a broad-host-range replicon of pWV01. In Lactococcus lactis, transformants carrying the vector were easily detectable by the appearance of a blue colony on a X-a-gal-containing medium and also by the growth on a medium containing melibiose as a sole carbon source. The expression/secretion vector was equipped with the controllable and strong nisA promoter. In addition, uSP45 signal peptide was inserted for the efficient secretion of a foreign protein outside cells. The vector pFMN30 was used for the expression and secretion of (x-amylase as a reporter gene, lacking a signal sequence derived from Bacillus licheniformis in L. lactis. These results show that the food-grade expression/secretion vector constructed in the present study could be used for the production of foreign proteins in L. lactis for the production food materials and also for the medicinal purposes. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:468 / 475
页数:8
相关论文
共 37 条
[1]   Controlled intra- or extracellular production of staphylococcal nuclease and ovine omega interferon in Lactococcus lactis [J].
Bermudez-Humarán, LG ;
Langella, P ;
Commissaire, J ;
Gilbert, S ;
Le Loir, Y ;
L'Haridon, R ;
Corthier, G .
FEMS MICROBIOLOGY LETTERS, 2003, 224 (02) :307-313
[2]   The complete genome sequence of the lactic acid bacterium Lactococcus lactis ssp lactis IL1403 [J].
Bolotin, A ;
Wincker, P ;
Mauger, S ;
Jaillon, O ;
Malarme, K ;
Weissenbach, J ;
Ehrlich, SD ;
Sorokin, A .
GENOME RESEARCH, 2001, 11 (05) :731-753
[3]   Novel food-grade plasmid vector based on melibiose fermentation for the genetic engineering of Lactococcus lactis [J].
Boucher, I ;
Parrot, M ;
Gaudreau, H ;
Champagne, CP ;
Vadeboncoeur, C ;
Moineau, S .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (12) :6152-6161
[4]  
de Vos WM, 1999, INT DAIRY J, V9, P3, DOI 10.1016/S0958-6946(99)00038-2
[5]   Engineering metabolic highways in Lactococci and other lactic acid bacteria [J].
de Vos, WM ;
Hugenholtz, J .
TRENDS IN BIOTECHNOLOGY, 2004, 22 (02) :72-79
[6]   Controlled gene expression systems for Lactococcus lactis with the food-grade inducer nisin [J].
deRuyter, PGGA ;
Kuipers, OP ;
deVos, WM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (10) :3662-3667
[7]   Molecular characterization of a theta replication plasmid and its use for development of a two-component food-grade cloning system for Lactococcus lactis [J].
Émond, É ;
Ée, RL ;
Drolet, G ;
Moineau, S ;
Lapointe, G .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (04) :1700-1709
[8]   DEVELOPMENT AND APPLICATION OF PFM011 AS A POSSIBLE FOOD-GRADE CLONING VECTOR [J].
FROSETH, BR ;
MCKAY, LL .
JOURNAL OF DAIRY SCIENCE, 1991, 74 (05) :1445-1453
[9]  
GASSON MJ, 1983, J BACTERIOL, V154, P1
[10]  
HANAHAN D, 1983, J MOL BIOL, V134, P318