Food-grade gene expression in lactic acid bacteria

被引:72
作者
Peterbauer, Clemens [1 ]
Maischberger, Thomas [1 ]
Haltrich, Dietmar [1 ]
机构
[1] BOKU Univ Nat Resources & Life Sci, Food Biotechnol Lab, Vienna, Austria
关键词
Food biotechnology; Gene expression; Lactobacillus; Lactococcus; Streptococcus; RECOMBINANT LACTOCOCCUS-LACTIS; ANTIFREEZE PROTEIN ANALOG; SITE-SPECIFIC INTEGRATION; HOST-VECTOR SYSTEM; LACTOBACILLUS-PLANTARUM; SELECTION MARKER; CLONING VECTOR; SUBSP LACTIS; STREPTOCOCCUS-THERMOPHILUS; BETA-GALACTOSIDASES;
D O I
10.1002/biot.201100034
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In the 1990s, significant efforts were invested in the research and development of food-grade expression systems in lactic acid bacteria (LAB). At this time, Lactococcus lactis in particular was demonstrated to be an ideal cell factory for the food-grade production of recombinant proteins. Steady progress has since been made in research on LAB, including Lactococcus, Lactobacillus and Streptococcus, in the areas of recombinant enzyme production, industrial food fermentation, and gene and metabolic pathway regulation. Over the past decade, this work has also led to new approaches on chromosomal integration vectors and host/vector systems. These newly constructed food-grade gene expression systems were designed with specific attention to self-cloning strategies, food-grade selection markers, plasmid replication and chromosomal gene replacements. In this review, we discuss some well-characterized chromosomal integration and food-grade host/vector systems used in LAB, with a special focus on sustainability, stability and overall safety, and give some attractive examples of protein expression that are based on these systems.
引用
收藏
页码:1147 / 1161
页数:15
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