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The Mithramycin Gene Cluster of Streptomyces Argillaceus Contains a Positive Regulatory Gene and Two Repeated DNA Sequences That Are Located at Both Ends of the Cluster

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1999 Jan 12
PMID 9882681
Citations 29
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Abstract

Sequencing of a 4.3-kb DNA region from the chromosome of Streptomyces argillaceus, a mithramycin producer, revealed the presence of two open reading frames (ORFs). The first one (orfA) codes for a protein that resembles several transport proteins. The second one (mtmR) codes for a protein similar to positive regulators involved in antibiotic biosynthesis (DnrI, SnoA, ActII-orf4, CcaR, and RedD) belonging to the Streptomyces antibiotic regulatory protein (SARP) family. Both ORFs are separated by a 1.9-kb, apparently noncoding region. Replacement of the mtmR region by an antibiotic resistance cassette completely abolished mithramycin biosynthesis. Expression of mtmR in a high-copy-number vector in S. argillaceus caused a 16-fold increase in mithramycin production. The mtmR gene restored actinorhodin production in Streptomyces coelicolor JF1 mutant, in which the actinorhodin-specific activator ActII-orf4 is inactive, and also stimulated actinorhodin production by Streptomyces lividans TK21. A 241-bp region located 1.9 kb upstream of mtmR was found to be repeated approximately 50 kb downstream of mtmR at the other end of the mithramycin gene cluster. A model to explain a possible route for the acquisition of the mithramycin gene cluster by S. argillaceus is proposed.

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References
1.
Lombo F, Blanco G, Fernandez E, Mendez C, Salas J . Characterization of Streptomyces argillaceus genes encoding a polyketide synthase involved in the biosynthesis of the antitumor mithramycin. Gene. 1996; 172(1):87-91. DOI: 10.1016/0378-1119(96)00029-7. View

2.
Liras P, Rodriguez-Garcia A, Martin J . A regulatory gene (ccaR) required for cephamycin and clavulanic acid production in Streptomyces clavuligerus: amplification results in overproduction of both beta-lactam compounds. J Bacteriol. 1997; 179(6):2053-9. PMC: 178932. DOI: 10.1128/jb.179.6.2053-2059.1997. View

3.
Ylihonko K, Tuikkanen J, Jussila S, Cong L, Mantsala P . A gene cluster involved in nogalamycin biosynthesis from Streptomyces nogalater: sequence analysis and complementation of early-block mutations in the anthracycline pathway. Mol Gen Genet. 1996; 251(2):113-20. DOI: 10.1007/BF02172908. View

4.
Fernandez E, Lombo F, Mendez C, Salas J . An ABC transporter is essential for resistance to the antitumor agent mithramycin in the producer Streptomyces argillaceus. Mol Gen Genet. 1996; 251(6):692-8. DOI: 10.1007/BF02174118. View

5.
Tatusov R, Mushegian A, Bork P, Brown N, Hayes W, Borodovsky M . Metabolism and evolution of Haemophilus influenzae deduced from a whole-genome comparison with Escherichia coli. Curr Biol. 1996; 6(3):279-91. DOI: 10.1016/s0960-9822(02)00478-5. View