J Med Microbiol 2007, 56: 480–486 PubMedCrossRef 78 Moura-Costa

J Med Microbiol 2007, 56: 480–486.PubMedCrossRef 78. Moura-Costa LF, Paule BJA, Azevedo V, Freire SM, Nascimento I, Schaer R, Regis LF, Vale VLC, Matos DP, Bahia RC, Carminati R, Meyer R: Chemically defined synthetic medium for Corynebacterium pseudotuberculosis culture. Rev. Bras. Saúde e Produção Animal 2002, 3: 1–9. 79. Nesvizhskii AI, Keller A, Kolker E, Aebersold R: A statistical model for identifying proteins

by tandem mass spectrometry. Anal Chem 2003, 75: 4646–4658.PubMedCrossRef 80. Silva JC, Denny R, Dorschel CA, Gorenstein M, Kass IJ, Li G, McKenna T, Nold MJ, Richardson K, Young P, Geromanos S: Quantitative proteomic analysis by accurate mass retention time pairs. Anal Chem 2005, 77: 2187–2200.PubMedCrossRef 81. Bendtsen JD, Nielsen PD-L1 mutation H, Widdick D, Palmer T, Brunak S: Prediction of twin-arginine signal peptides.

BMC Bioinformatics 2005, 6: 167.PubMedCrossRef 82. Wittkop T, Emig D, Lange S, Rahmann S, Albrecht M, Morris JH, Böcker S, Stoye J, Baumbach J: Partitioning biological data with transitivity clustering. Nat Methods 2010, 7: 419–420.PubMedCrossRef 83. Baumbach J, Wittkop T, Kleindt CK, Tauch A: Integrated analysis and reconstruction of microbial transcriptional gene regulatory networks using CoryneRegNet. Nat Protoc 2009, 4: 992–1005.PubMedCrossRef 84. Götz S, García-Gómez LY2835219 molecular weight JM, Terol J, Williams TD, Nagaraj SH, Nueda MJ, Robles M, Talón M, Dopazo J, Conesa A: High-throughput functional annotation and data mining with the Blast2GO suite. Nucleic Acids Res 2008, 36: 3420–3435.PubMedCrossRef Competing interests The authors declare that they have no competing interests. Authors’ contributions LGCP, SES, LMF, MARC, AMCP, RM, AS, JHS, SCO, AM, CGD, and VA conceived the idea, participated in the design of the study, and critically read the manuscript. C-X-C chemokine receptor type 7 (CXCR-7) LGCP, SES, NS, TLPC, WMS, AGV, and SGS performed microbiological and/or proteomic experiments. LGCP, SES and ARS performed

bioinformatical analyses. LGCP and SES wrote the manuscript. All authors read and approved the final manuscript.”
“Background Filamentous fungi produce unique proteins called hydrophobins that are secreted and cover the walls of spores and hyphae with a hydrophobic layer [1]. Structurally, hydrophobins are characterised by their small size and the presence of eight cysteine residues which are arranged in a conserved array and form four pairs of disulphide bridges. By their ability to aggregate to amphipathic membranes, they attach to the surface of the hydrophilic fungal cell wall, thereby exposing the hydrophobic layer to the selleck outside [2]. By scanning electron microscopy, hydrophobin layers can often be recognised by the formation of rodlets of characteristic dimensions [3]. Hydrophobin aggregates are highly resistant against treatments that are used for solubilising proteins.

Comments are closed.