Literature DB >> 24421196

Biosynthesis of a trypanocide by Chromobacterium violaceum.

N Durán1, R V Antonio, M Haun, R A Pilli.   

Abstract

Radio-isotope studies indicated not only that L-tryptophan can serve as carbon source for synthesis of the trypanocide, violacein by Chromobacterium violaceum (BB-78 strain) but also that isatin and indole 3-acetic acid are both important metabolic intermediates. Using 3-indolyl [2-(14)C] and [1-(14)C] acetic acid, it was found that the carboxylic carbon was not eliminated and that indole-3-acetic acid was incorporated intact into the pigment structure. N-Ethyl(5-hydroxy-indol-3-yl)-2-indolylethylamide is also an important metabolic intermediate in the violacein biosynthesis. This is the first report of a metabolic scheme for violacein synthesis which includes an intermediate other than L-tryptophan.

Entities:  

Year:  1994        PMID: 24421196     DOI: 10.1007/BF00327960

Source DB:  PubMed          Journal:  World J Microbiol Biotechnol        ISSN: 0959-3993            Impact factor:   3.312


  10 in total

1.  Divergent pathways of indole metabolism in Chromobacterium violaceum.

Authors:  O K SEBEK; H JAGER
Journal:  Nature       Date:  1962-11-24       Impact factor: 49.962

2.  Incorporation of C14-labeled substrates into violacein.

Authors:  R D DEMOSS; N R EVANS
Journal:  J Bacteriol       Date:  1960-05       Impact factor: 3.490

3.  5-Hydroxytryptophan formation and tryptophan metabolism in Chromobacterium violaceum.

Authors:  C MITOMA; H WEISSBACH; S UDENFRIEND
Journal:  Arch Biochem Biophys       Date:  1956-07       Impact factor: 4.013

4.  Formation of indole-3-carboxylic acid by Chromobacterium violaceum.

Authors:  P J Davis; M E Gustafson; J P Rosazza
Journal:  J Bacteriol       Date:  1976-04       Impact factor: 3.490

Review 5.  Applications of stereoselectivity of enzymes: synthesis of optically active amino acids and alpha-hydroxy acids, and stereospecific isotope-labeling of amino acids, amines and coenzymes.

Authors:  K Yonaha; K Soda
Journal:  Adv Biochem Eng Biotechnol       Date:  1986       Impact factor: 2.635

6.  Bacterial chemistry-III: preliminary studies on trypanosomal activities of Chromobacterium violaceum products.

Authors:  N Durán; V Campos; R Riveros; A Joyas; M F Pereira; M Haun
Journal:  An Acad Bras Cienc       Date:  1989-03       Impact factor: 1.753

7.  The bacterial oxidation of indole.

Authors:  M Fujioka; H Wada
Journal:  Biochim Biophys Acta       Date:  1968-04-16

8.  Singlet oxygen formation during peroxidase catalyzed degradation of carcinogenic N-nitrosamine.

Authors:  N Durán; A Faljoni
Journal:  Biochem Biophys Res Commun       Date:  1978-07-14       Impact factor: 3.575

9.  Bacterial chemistry. VI. Biological activities and cytotoxicity of 1,3-dihydro-2H-indol-2-one derivatives.

Authors:  M Haun; M F Pereira; M E Hoffmann; A Joyas; V Campos; L D Filardi; S L de Castro; N Duran
Journal:  Biol Res       Date:  1992       Impact factor: 5.612

10.  Effect of growth conditions on production of violacein by Chromobacterium violaceum (BB-78 strain).

Authors:  R Riveros; M Haun; N Durán
Journal:  Braz J Med Biol Res       Date:  1989       Impact factor: 2.590

  10 in total
  11 in total

1.  Expression, crystallization and preliminary crystallographic data analysis of VioD, a hydroxylase in the violacein-biosynthesis pathway.

Authors:  Tingting Ran; Mengxiao Gao; Qiaoe Wei; Jianhua He; Lin Tang; Weiwu Wang; Dongqing Xu
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2015-01-28       Impact factor: 1.056

2.  Purple-pigmented violacein-producing Duganella spp. inhabit the rhizosphere of wild and cultivated olives in southern Spain.

Authors:  Sergio Aranda; Miguel Montes-Borrego; Blanca B Landa
Journal:  Microb Ecol       Date:  2011-03-22       Impact factor: 4.552

3.  Violacein cytotoxicity and induction of apoptosis in V79 cells.

Authors:  P S Melo; S S Maria; B C Vidal; M Haun; N Durán
Journal:  In Vitro Cell Dev Biol Anim       Date:  2000-09       Impact factor: 2.416

4.  Diversity in antifungal activity of strains of Chromobacterium violaceum from the Brazilian Amazon.

Authors:  Eriana Serpa Barreto; Adalgisa Ribeiro Torres; Marliton Rocha Barreto; Ana Tereza Ribeiro Vasconcelos; Spartaco Astolfi-Filho; Mariangela Hungria
Journal:  J Ind Microbiol Biotechnol       Date:  2008-03-18       Impact factor: 3.346

5.  The complete genome sequence of Chromobacterium violaceum reveals remarkable and exploitable bacterial adaptability.

Authors: 
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-18       Impact factor: 11.205

6.  Identification of N-acyl-l-homoserine lactones produced by non-pigmented Chromobacterium aquaticum CC-SEYA-1(T) and pigmented Chromobacterium subtsugae PRAA4-1(T).

Authors:  P D Rekha; Chiu-Chung Young; A B Arun
Journal:  3 Biotech       Date:  2011-10-14       Impact factor: 2.406

7.  Proteomic analysis of Chromobacterium violaceum and its adaptability to stress.

Authors:  Diogo Castro; Isabelle Bezerra Cordeiro; Paula Taquita; Marcos Nogueira Eberlin; Jerusa Simone Garcia; Gustavo Henrique M F Souza; Marco Aurélio Zezzi Arruda; Edmar V Andrade; Spartaco A Filho; J Lee Crainey; Luis Lopez Lozano; Paulo A Nogueira; Patrícia P Orlandi
Journal:  BMC Microbiol       Date:  2015-12-01       Impact factor: 3.605

8.  Violacein induces cell death by triggering mitochondrial membrane hyperpolarization in vitro.

Authors:  Angélica Maria de Sousa Leal; Jana Dara Freires de Queiroz; Silvia Regina Batistuzzo de Medeiros; Tatjana Keesen de Souza Lima; Lucymara Fassarella Agnez-Lima
Journal:  BMC Microbiol       Date:  2015-06-06       Impact factor: 3.605

9.  High crude violacein production from glucose by Escherichia coli engineered with interactive control of tryptophan pathway and violacein biosynthetic pathway.

Authors:  Ming-Yue Fang; Chong Zhang; Song Yang; Jin-Yu Cui; Pei-Xia Jiang; Kai Lou; Masaaki Wachi; Xin-Hui Xing
Journal:  Microb Cell Fact       Date:  2015-01-16       Impact factor: 5.328

10.  Antiplasmodial and trypanocidal activity of violacein and deoxyviolacein produced from synthetic operons.

Authors:  Elizabeth Bilsland; Tatyana A Tavella; Renata Krogh; Jamie E Stokes; Annabelle Roberts; James Ajioka; David R Spring; Adriano D Andricopulo; Fabio T M Costa; Stephen G Oliver
Journal:  BMC Biotechnol       Date:  2018-04-11       Impact factor: 2.563

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