Literature DB >> 14702394

The importance of the Tat-dependent protein secretion pathway in Streptomyces as revealed by phenotypic changes in tat deletion mutants and genome analysis.

Kristien Schaerlaekens1, Lieve Van Mellaert, Elke Lammertyn, Nick Geukens, Jozef Anné.   

Abstract

Streptomyces are Gram-positive soil bacteria that are used industrially, not only as a source of medically important natural compounds, but also as a host for the secretory production of a number of heterologous proteins. A good understanding of the different secretion processes in this organism is therefore of major importance. The functionality of the recently discovered bacterial twin-arginine translocation (Tat) pathway has already been shown in Streptomyces lividans. Here, the aberrant phenotype of S. lividans DeltatatB and DeltatatC single mutants is described. Both mutants are characterized by a dispersed growth in liquid medium, an impaired morphological differentiation on solid medium and growth retardation. To reveal the extent to which the Tat pathway is used in Streptomyces, putative Tat-dependent precursor proteins of Streptomyces coelicolor, a very close relative of S. lividans, and of Streptomyces avermitilis, of which the genomes have been completely sequenced, were identified by a modified version of the TATFIND computer program designed by Rose and colleagues [Rose, R. W., Brüser, T., Kissinger, J. C. & Pohlschröder, M. (2002). Mol Microbiol 45, 943-950]. A list of 230 precursor proteins was obtained; this is the highest number of putative Tat substrates found in any genome so far. In addition to the Streptomyces antibioticus tyrosinase, it was also demonstrated that the secretion of the S. lividans xylanase C is Tat-dependent. The predicted Tat substrates belong to a variety of protein classes, with a high number of proteins functioning in degradation of macromolecules, in binding and transport, and in secondary metabolism. Only a minor fraction of the proteins seem to bind a cofactor. The aberrant phenotype of the DeltatatB and DeltatatC mutants together with the high number of putative Tat-dependent substrates suggests that the Streptomyces Tat pathway has a distinct and more important role in protein secretion than in most other bacteria.

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Year:  2004        PMID: 14702394     DOI: 10.1099/mic.0.26684-0

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  15 in total

Review 1.  The bacterial twin-arginine translocation pathway.

Authors:  Philip A Lee; Danielle Tullman-Ercek; George Georgiou
Journal:  Annu Rev Microbiol       Date:  2006       Impact factor: 15.500

2.  Exploring the Feasibility of the Sec Route to Secrete Proteins Using the Tat Route in Streptomyces lividans.

Authors:  Sonia Gullón; Rebeca L Vicente; José R Valverde; Silvia Marín; Rafael P Mellado
Journal:  Mol Biotechnol       Date:  2015-10       Impact factor: 2.695

3.  Characterization of the twin-arginine translocase secretion system of Mycobacterium smegmatis.

Authors:  James E Posey; Thomas M Shinnick; Frederick D Quinn
Journal:  J Bacteriol       Date:  2006-02       Impact factor: 3.490

4.  The twin-arginine translocation pathway of Mycobacterium smegmatis is functional and required for the export of mycobacterial beta-lactamases.

Authors:  Justin A McDonough; Kari E Hacker; Anthony R Flores; Martin S Pavelka; Miriam Braunstein
Journal:  J Bacteriol       Date:  2005-11       Impact factor: 3.490

5.  Function and redundancy of the chaplin cell surface proteins in aerial hypha formation, rodlet assembly, and viability in Streptomyces coelicolor.

Authors:  Christina Di Berardo; David S Capstick; Maureen J Bibb; Kim C Findlay; Mark J Buttner; Marie A Elliot
Journal:  J Bacteriol       Date:  2008-06-27       Impact factor: 3.490

6.  Aclacinomycin oxidoreductase (AknOx) from the biosynthetic pathway of the antibiotic aclacinomycin is an unusual flavoenzyme with a dual active site.

Authors:  Igor Alexeev; Azmiri Sultana; Pekka Mäntsälä; Jarmo Niemi; Gunter Schneider
Journal:  Proc Natl Acad Sci U S A       Date:  2007-03-29       Impact factor: 11.205

7.  Role of the twin arginine protein transport pathway in the assembly of the Streptomyces coelicolor cytochrome bc1 complex.

Authors:  Adam Hopkins; Grant Buchanan; Tracy Palmer
Journal:  J Bacteriol       Date:  2013-10-18       Impact factor: 3.490

8.  The twin-arginine translocation pathway is a major route of protein export in Streptomyces coelicolor.

Authors:  David A Widdick; Kieran Dilks; Govind Chandra; Andrew Bottrill; Mike Naldrett; Mechthild Pohlschröder; Tracy Palmer
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-08       Impact factor: 11.205

9.  Dynamic localization of Tat protein transport machinery components in Streptomyces coelicolor.

Authors:  Joost Willemse; Beata Ruban-Ośmialowska; David Widdick; Katherine Celler; Matthew I Hutchings; Gilles P van Wezel; Tracy Palmer
Journal:  J Bacteriol       Date:  2012-09-21       Impact factor: 3.490

10.  LocateP: genome-scale subcellular-location predictor for bacterial proteins.

Authors:  Miaomiao Zhou; Jos Boekhorst; Christof Francke; Roland J Siezen
Journal:  BMC Bioinformatics       Date:  2008-03-27       Impact factor: 3.169

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