Protein secretion in Lactococcus lactis:: an efficient way to increase the overall heterologous protein production -: art. no. 2

被引:167
作者
Le Loir, Y
Azevedo, V
Oliveira, SC
Freitas, DA
Miyoshi, A
Bermúdez-Humarán, LG
Nouaille, S
Ribeiro, LA
Leclercq, S
Gabriel, JE
Guimaraes, VD
Oliveira, MN
Charlier, C
Gautier, M
Langella, P
机构
[1] INRA, Microbiol Lab, UMR 1253, STLO, F-35042 Rennes, France
[2] Univ Fed Minas Gerais, Inst Ciencias Biol, Belo Horizonte, MG, Brazil
[3] INRA, Unite Rech Laitieres & Genet Appl, F-78352 Jouy En Josas, France
关键词
D O I
10.1186/1475-2859-4-2
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
Lactococcus lactis, the model lactic acid bacterium (LAB), is a food grade and well-characterized Gram positive bacterium. It is a good candidate for heterologous protein delivery in foodstuff or in the digestive tract. L. lactis can also be used as a protein producer in fermentor. Many heterologous proteins have already been produced in L. lactis but only few reports allow comparing production yields for a given protein either produced intracellularly or secreted in the medium. Here, we review several works evaluating the influence of the localization on the production yields of several heterologous proteins produced in L. lactis. The questions of size limits, conformation, and proteolysis are addressed and discussed with regard to protein yields. These data show that i) secretion is preferable to cytoplasmic production; ii) secretion enhancement (by signal peptide and propeptide optimization) results in increased production yield; iii) protein conformation rather than protein size can impair secretion and thus alter production yields; and iv) fusion of a stable protein can stabilize labile proteins. The role of intracellular proteolysis on heterologous cytoplasmic proteins and precursors is discussed. The new challenges now are the development of food grade systems and the identification and optimization of host factors affecting heterologous protein production not only in L. lactis, but also in other LAB species.
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页数:13
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共 79 条
[1]   Heterologous gene expression of bovine plasmin in Lactococcus lactis [J].
Arnau, J ;
HjerlHansen, E ;
Israelsen, H .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1997, 48 (03) :331-338
[2]   Fusion to a carrier protein and a synthetic propeptide enhances E7 HPV-16 production and secretion in Lactococcus lactis [J].
Bermúdez-Humarán, LG ;
Cortes-Perez, NG ;
Le Loir, Y ;
Gruss, A ;
Rodriguez-Padilla, C ;
Saucedo-Cardenas, O ;
Langella, P ;
de Oca-Luna, RM .
BIOTECHNOLOGY PROGRESS, 2003, 19 (03) :1101-1104
[3]   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
[4]   Intranasal immunization with recombinant Lactococcus lactis secreting murine interleukin-12 enhances antigen-specific Th1 cytokine production [J].
Bermúdez-Humarán, LG ;
Langella, P ;
Cortes-Perez, NG ;
Gruss, A ;
Tamez-Guerra, RS ;
Oliveira, SC ;
Saucedo-Cardenas, O ;
de Oca-Luna, RM ;
Le Loir, Y .
INFECTION AND IMMUNITY, 2003, 71 (04) :1887-1896
[5]   Production of human papillomavirus type 16 E7 protein in Lactococcus lactis [J].
Bermúdez-Humarán, LG ;
Langella, P ;
Miyoshi, A ;
Gruss, A ;
Guerra, RT ;
de Oca-Luna, RM ;
Le Loir, Y .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (02) :917-922
[6]   Lactobacillus bulgaricus proteinase expressed in Lactococcus lactis is a powerful carrier for cell wall-associated and secreted bovine β-lactoglobulin fusion proteins [J].
Bernasconi, E ;
Germond, JE ;
Delley, M ;
Fritsché, R ;
Corthésy, B .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (06) :2917-2923
[7]   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
[8]   Improving protein secretion by engineering components of the bacterial translocation machinery [J].
Braun, P ;
Gerritse, G ;
van Dijl, JM ;
Quax, WJ .
CURRENT OPINION IN BIOTECHNOLOGY, 1999, 10 (04) :376-381
[9]   Heteromeric geranyl diphosphate synthase from mint: construction of a functional fusion protein and inhibition by bisphosphonate substrate analogs [J].
Burke, C ;
Klettke, K ;
Croteau, R .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2004, 422 (01) :52-60
[10]   The S-layer gene of Lactobacillus helveticus CNRZ 892:: cloning, sequence and heterologous expression [J].
Callegari, ML ;
Riboli, B ;
Sanders, JW ;
Cocconcelli, PS ;
Kok, J ;
Venema, G ;
Morelli, L .
MICROBIOLOGY-SGM, 1998, 144 :719-726