Genome-wide analysis of signal peptide functionality in Lactobacillus plantarum WCFS1

被引:85
|
作者
Mathiesen, Geir [1 ]
Sveen, Anita [1 ]
Brurberg, May Bente [2 ]
Fredriksen, Lasse [1 ]
Axelsson, Lars [3 ]
Eijsink, Vincent G. H. [1 ]
机构
[1] Norwegian Univ Life Sci, Ctr Mol Microbiol, Dept Chem Biotechnol & Food Sci, N-1432 As, Norway
[2] Norwegian Inst Agr & Environm Res, Plant Hlth & Plant Protect Div, N-1432 As, Norway
[3] Norfima Mat, N-1430 As, Norway
来源
BMC GENOMICS | 2009年 / 10卷
关键词
HETEROLOGOUS PROTEIN SECRETION; LACTIC-ACID BACTERIA; INDUCIBLE GENE-EXPRESSION; GRAM-POSITIVE BACTERIA; BACILLUS-SUBTILIS; LACTOCOCCUS-LACTIS; ALPHA-AMYLASE; HIGH-LEVEL; SURFACE-PROTEINS; SYSTEM;
D O I
10.1186/1471-2164-10-425
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
Background: Lactobacillus plantarum is a normal, potentially probiotic, inhabitant of the human gastrointestinal (GI) tract. The bacterium has great potential as food-grade cell factory and for in situ delivery of biomolecules. Since protein secretion is important both for probiotic activity and in biotechnological applications, we have carried out a genome-wide experimental study of signal peptide (SP) functionality. Results: We have constructed a library of 76 Sec-type signal peptides from L. plantarum WCFS1 that were predicted to be cleaved by signal peptidase I. SP functionality was studied using staphylococcal nuclease (NucA) as a reporter protein. 82% of the SPs gave significant extracellular NucA activity. Levels of secreted NucA varied by a dramatic 1800-fold and this variation was shown not to be the result of different mRNA levels. For the best-performing SPs all produced NucA was detected in the culture supernatant, but the secretion efficiency decreased for the less well performing SPs. Sequence analyses of the SPs and their cognate proteins revealed four properties that correlated positively with SP performance for NucA: high hydrophobicity, the presence of a transmembrane helix predicted by TMHMM, the absence of an anchoring motif in the cognate protein, and the length of the H+C domain. Analysis of a subset of SPs with a lactobacillal amylase (AmyA) showed large variation in production levels and secretion efficiencies. Importantly, there was no correlation between SP performance with NucA and the performance with AmyA. Conclusion: This is the first comprehensive experimental study showing that predicted SPs in the L. plantarum genome actually are capable of driving protein secretion. The results reveal considerable variation between the SPs that is at least in part dependent on the protein that is secreted. Several SPs stand out as promising candidates for efficient secretion of heterologous proteins in L. plantarum. The results for NucA provide some hints as to the sequence-based prediction of SP functionality, but the general conclusion is that such prediction is difficult. The vector library generated in this study is based on exchangeable cassettes and provides a powerful tool for rapid experimental screening of SPs.
引用
收藏
页数:13
相关论文
共 50 条
  • [41] Unravelling the diversity of glycoside hydrolase family 13 α-amylases from Lactobacillus plantarum WCFS1
    Plaza-Vinuesa, Laura
    Hernandez-Hernandez, Oswaldo
    Javier Moreno, F.
    de las Rivas, Blanca
    Munoz, Rosario
    MICROBIAL CELL FACTORIES, 2019, 18 (01)
  • [42] Population Heterogeneity of Lactobacillus plantarum WCFS1 Microcolonies in Response to and Recovery from Acid Stress
    Ingham, Colin J.
    Beerthuyzen, Marke
    Vlieg, Johan van Hylckama
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (24) : 7750 - 7758
  • [43] Structure, biochemical characterization and analysis of the pleomorphism of carboxylesterase Cest-2923 from Lactobacillus plantarum WCFS1
    Benavente, Rocio
    Esteban-Torres, Maria
    Acebron, Ivan
    de las Rivas, Blanca
    Munoz, Rosario
    Alvarez, Yanaisis
    Mancheno, Jose M.
    FEBS JOURNAL, 2013, 280 (24) : 6658 - 6671
  • [44] Interactions between formulation and spray drying conditions related to survival of Lactobacillus plantarum WCFS1
    Perdana, Jimmy
    Fox, Martijn B.
    Siwei, Chen
    Boom, Remko M.
    Schutyser, Maarten A. I.
    FOOD RESEARCH INTERNATIONAL, 2014, 56 : 9 - 17
  • [45] Identification of key peptidoglycan hydrolases for morphogenesis, autolysis, and peptidoglycan composition of Lactobacillus plantarum WCFS1
    Rolain, Thomas
    Bernard, Elvis
    Courtin, Pascal
    Bron, Peter A.
    Kleerebezem, Michiel
    Chapot-Chartier, Marie-Pierre
    Hols, Pascal
    MICROBIAL CELL FACTORIES, 2012, 11
  • [46] Reversibility of membrane permeabilization upon pulsed electric field treatment in Lactobacillus plantarum WCFS1
    Vaessen, E. M. J.
    Timmermans, R. A. H.
    Tempelaars, M. H.
    Schutyser, M. A. I.
    den Besten, H. M. W.
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [47] Comparative Analysis of Lactobacillus plantarum WCFS1 Transcriptomes by Using DNA Microarray and Next-Generation Sequencing Technologies
    Leimena, Milkha M.
    Wels, Michiel
    Bongers, Roger S.
    Smid, Eddy J.
    Zoetendal, Erwin G.
    Kleerebezem, Michiel
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2012, 78 (12) : 4141 - 4148
  • [48] β-Galactosidase from Lactobacillus plantarum WCFS1: biochemical characterization and formation of prebiotic galacto-oligosaccharides
    Iqbal, Sanaullah
    Nguyen, Thu-Ha
    Tien Thanh Nguyen
    Maischberger, Thomas
    Haltrich, Dietmar
    CARBOHYDRATE RESEARCH, 2010, 345 (10) : 1408 - 1416
  • [49] Overexpression, Purification, and Biochemical Characterization of the Esterase Est0796 from Lactobacillus plantarum WCFS1
    Navarro-González Inmaculada
    Sánchez-Ferrer Álvaro
    García-Carmona Francisco
    Molecular Biotechnology, 2013, 54 : 651 - 660
  • [50] Unravelling the carbohydrate specificity of MelA from Lactobacillus plantarum WCFS1: An α-galactosidase displaying regioselective transgalactosylation
    Delgado-Fernandez, Paloma
    Plaza-Vinuesa, Laura
    Hernandez-Hernandez, Oswaldo
    de las Rivas, Blanca
    Corzo, Nieves
    Munoz, Rosario
    Javier Moreno, F.
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2020, 153 : 1070 - 1079