Literature DB >> 9822824

A surface active protein involved in aerial hyphae formation in the filamentous fungus Schizophillum commune restores the capacity of a bald mutant of the filamentous bacterium Streptomyces coelicolor to erect aerial structures.

R D Tillotson1, H A Wösten, M Richter, J M Willey.   

Abstract

The filamentous bacterium Streptomyces coelicolor undergoes a complex process of morphological differentiation involving the formation of a dense lawn of aerial hyphae that grow away from the colony surface into the air to form an aerial mycelium. Bald mutants of S. coelicolor, which are blocked in aerial mycelium formation, regain the capacity to erect aerial structures when exposed to a small hydrophobic protein called SapB, whose synthesis is temporally and spatially correlated with morphological differentiation. We now report that SapB is a surfactant that is capable of reducing the surface tension of water from 72 mJ m-2 to 30 mJ m-2 at a concentration of 50 microgram ml-1. We also report that SapB, like the surface-active peptide streptofactin produced by the species S. tendae, was capable of restoring the capacity of bald mutants of S. tendae to erect aerial structures. Strikingly, a member (SC3) of the hydrophobin family of fungal proteins involved in the erection of aerial hyphae in the filamentous fungus Schizophyllum commune was also capable of restoring the capacity of S. coelicolor and S. tendae bald mutants to erect aerial structures. SC3 is unrelated in structure to SapB and streptofactin but, like the streptomycetes proteins, the fungal protein is a surface active agent. Scanning electron microscopy revealed that aerial structures produced in response to both the bacterial or the fungal proteins were undifferentiated vegetative hyphae that had grown away from the colony surface but had not commenced the process of spore formation. We conclude that the production of SapB and streptofactin at the start of morphological differentiation contributes to the erection of aerial hyphae by decreasing the surface tension at the colony surface but that subsequent morphogenesis requires additional developmentally regulated events under the control of bald genes.

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Year:  1998        PMID: 9822824     DOI: 10.1046/j.1365-2958.1998.01093.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  27 in total

1.  Differentiation and anaerobiosis in standing liquid cultures of Streptomyces coelicolor.

Authors:  Geertje van Keulen; Henk M Jonkers; Dennis Claessen; Lubbert Dijkhuizen; Han A B Wösten
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

Review 2.  Prokaryotic development: emerging insights.

Authors:  Lee Kroos; Janine R Maddock
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

3.  A novel class of secreted hydrophobic proteins is involved in aerial hyphae formation in Streptomyces coelicolor by forming amyloid-like fibrils.

Authors:  Dennis Claessen; Rick Rink; Wouter de Jong; Jeroen Siebring; Peter de Vreugd; F G Hidde Boersma; Lubbert Dijkhuizen; Han A B Wosten
Journal:  Genes Dev       Date:  2003-06-27       Impact factor: 11.361

4.  The chaplins: a family of hydrophobic cell-surface proteins involved in aerial mycelium formation in Streptomyces coelicolor.

Authors:  Marie A Elliot; Nitsara Karoonuthaisiri; Jianqiang Huang; Maureen J Bibb; Stanley N Cohen; Camilla M Kao; Mark J Buttner
Journal:  Genes Dev       Date:  2003-06-27       Impact factor: 11.361

5.  The SapB morphogen is a lantibiotic-like peptide derived from the product of the developmental gene ramS in Streptomyces coelicolor.

Authors:  Shinya Kodani; Michael E Hudson; Marcus C Durrant; Mark J Buttner; Justin R Nodwell; Joanne M Willey
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-26       Impact factor: 11.205

Review 6.  Taxonomy, Physiology, and Natural Products of Actinobacteria.

Authors:  Essaid Ait Barka; Parul Vatsa; Lisa Sanchez; Nathalie Gaveau-Vaillant; Cedric Jacquard; Jan P Meier-Kolthoff; Hans-Peter Klenk; Christophe Clément; Yder Ouhdouch; Gilles P van Wezel
Journal:  Microbiol Mol Biol Rev       Date:  2015-11-25       Impact factor: 11.056

7.  The bldC developmental locus of Streptomyces coelicolor encodes a member of a family of small DNA-binding proteins related to the DNA-binding domains of the MerR family.

Authors:  Alison C Hunt; Luis Servín-González; Gabriella H Kelemen; Mark J Buttner
Journal:  J Bacteriol       Date:  2005-01       Impact factor: 3.490

Review 8.  Decoding microbial chatter: cell-cell communication in bacteria.

Authors:  Karen L Visick; Clay Fuqua
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

Review 9.  Streptomyces morphogenetics: dissecting differentiation in a filamentous bacterium.

Authors:  Klas Flärdh; Mark J Buttner
Journal:  Nat Rev Microbiol       Date:  2009-01       Impact factor: 60.633

10.  Rhamnolipid surfactant production affects biofilm architecture in Pseudomonas aeruginosa PAO1.

Authors:  Mary E Davey; Nicky C Caiazza; George A O'Toole
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

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