Literature DB >> 8535506

Ectopic expression of the Streptomyces coelicolor whiE genes for polyketide spore pigment synthesis and their interaction with the act genes for actinorhodin biosynthesis.

T W Yu1, D A Hopwood.   

Abstract

The whiE gene cluster of Streptomyces coelicolor is normally expressed shortly before sporulation in the aerial mycelium, leading to production of the grey polyketide spore pigment. By placing the whiE genes under the control of the thiostrepton-inducible tipA promoter, they were artificially expressed on plasmids or in the chromosome during vegetative growth in a strain deleted for the act genes, which control biosynthesis of the polyketide antibiotic actinorhodin. Certain combinations of whiE-ORFI-VII led to production of mycelial pigments; these were exported into the medium when whiE-ORFI was absent, but poorly in its presence. Combined with comparative sequence data, the results allowed deductions to be made, or confirmed, about the normal roles of the eight known genes, whiE-ORFI-VIII, as follows: whiE-ORFIII, IV, V encode the three components (ketosynthase, chain length factor and acyl carrier protein) of the whiE 'minimal' polyketide synthase (PKS) needed for assembly of the carbon chain of the spore pigment precursor; whiE-ORFII, VI, VII are likely to be involved in cyclizations of the nascent carbon chain; whiE-ORFVIII controls a late step in the spore pigment biosynthetic pathway, probably a hydroxylation; and whiE-ORFI may encode a protein needed for correct targeting or retention of spore pigment at an appropriate cellular location. In other experiments, genes encoding components of the act-PKS and whiE-PKS were artificially co-expressed. Each of the three whiE minimal PKS subunit genes could complement lesions in the corresponding act-PKS genes to produce actinorhodin or related mycelial pigments, and each of the three act minimal PKS genes could complement lesions in the whiE minimal PKS genes to cause spore pigmentation. Thus the two sets of PKS subunits, which are encoded by genes that have presumably diverged from a common ancestor, are still capable of biochemical 'cross-talk', but this is normally prevented because the gene sets are expressed in different 'tissues' of the differentiated Streptomyces colony. Ectopic expression of sets of whiE-PKS genes presumed to be sufficient to assemble a carbon chain caused inhibition of early growth of the strains, perhaps by causing interference with fatty acid biosynthesis; this yielded circumstantial evidence that the whiE-PKS gene products can also interact with those of the fatty acid synthase(s) of the organism.

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Year:  1995        PMID: 8535506     DOI: 10.1099/13500872-141-11-2779

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


  24 in total

Review 1.  Microbial relatives of the seed storage proteins of higher plants: conservation of structure and diversification of function during evolution of the cupin superfamily.

Authors:  J M Dunwell; S Khuri; P J Gane
Journal:  Microbiol Mol Biol Rev       Date:  2000-03       Impact factor: 11.056

2.  Genomewide insertional mutagenesis in Streptomyces coelicolor reveals additional genes involved in morphological differentiation.

Authors:  A M Gehring; J R Nodwell; S M Beverley; R Losick
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-15       Impact factor: 11.205

3.  Generalized transduction in Streptomyces coelicolor.

Authors:  J Burke; D Schneider; J Westpheling
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-15       Impact factor: 11.205

4.  An orphan histidine kinase, OhkA, regulates both secondary metabolism and morphological differentiation in Streptomyces coelicolor.

Authors:  Yinhua Lu; Juanmei He; Hong Zhu; Zhenyu Yu; Rui Wang; Yunliang Chen; Fujun Dang; Weiwen Zhang; Sheng Yang; Weihong Jiang
Journal:  J Bacteriol       Date:  2011-04-22       Impact factor: 3.490

5.  A new GntR family transcriptional regulator in streptomyces coelicolor is required for morphogenesis and antibiotic production and controls transcription of an ABC transporter in response to carbon source.

Authors:  Brandan Hillerich; Janet Westpheling
Journal:  J Bacteriol       Date:  2006-08-25       Impact factor: 3.490

Review 6.  Biogenesis of antibiotics-viewing its history and glimpses of the future.

Authors:  J Spížek; K Sigler; T Řezanka; A Demain
Journal:  Folia Microbiol (Praha)       Date:  2016-05-18       Impact factor: 2.099

7.  Insight into the molecular basis of aromatic polyketide cyclization: crystal structure and in vitro characterization of WhiE-ORFVI.

Authors:  Ming-Yue Lee; Brian D Ames; Shiou-Chuan Tsai
Journal:  Biochemistry       Date:  2012-03-30       Impact factor: 3.162

8.  Developmental regulation of transcription of whiE, a locus specifying the polyketide spore pigment in Streptomyces coelicolor A3 (2)

Authors:  G H Kelemen; P Brian; K Flärdh; L Chamberlin; K F Chater; M J Buttner
Journal:  J Bacteriol       Date:  1998-05       Impact factor: 3.490

9.  Improvement of natamycin production by engineering of phosphopantetheinyl transferases in Streptomyces chattanoogensis L10.

Authors:  Hui Jiang; Yue-Yue Wang; Xin-Xin Ran; Wei-Ming Fan; Xin-Hang Jiang; Wen-Jun Guan; Yong-Quan Li
Journal:  Appl Environ Microbiol       Date:  2013-03-22       Impact factor: 4.792

10.  Relationships between fatty acid and polyketide synthases from Streptomyces coelicolor A3(2): characterization of the fatty acid synthase acyl carrier protein.

Authors:  W P Revill; M J Bibb; D A Hopwood
Journal:  J Bacteriol       Date:  1996-10       Impact factor: 3.490

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