[1] J.B. Laursen, J. Nielsen, Phenazine natural products: Biosynthesis, synthetic analogues, and biological activity, Chem. Rev. 104 (3) (2004) 1663-1686.[2] D.V. Mavrodi, W. Blankenfeldt, L.S. Thomashow, Phenazine compounds in fluorescent Pseudomonas spp. biosynthesis and regulation, Annu. Rev. Phytopathol. 44 (2006) 417-445.[3] A. Price-Whelan, L.E. Dietrich, D.K. Newman, Rethinking ‘secondary’ metabolism: physiological roles for phenazine antibiotics, Nat. Chem. Biol. 2 (4) (2006) 71-78.[4] D.V. Mavrodi, T.L. Peever, O.V. Mavrodi, J.A. Parejko, Diversity and evolution of the phenazine biosynthesis pathway, Appl. Environ. Microbiol. 76 (3) (2010) 866-879.[5] Cimmino, A.A. Evidente, V. Mathieu, A. Andolfi, Phenazines and cancer, Nat. Prod. Rep. 29 (4) (2012) 487-501.[6] L.S. Thomashow, D.M. Weller, R.F. Bonsall, L.S. Pierson, Production of the antibiotic phenazine-1-carboxylic acid by fluorescent Pseudomonas species in the rhizosphere of wheat, Appl. Environ. Microbiol. 56 (4) (1990) 908-912.[7] G.S. Jayatilake,M.P. Thornton, A.C. Leonard, J.E. Grimwade, Metabolites from an antarctic sponge-associated bacterium, Pseudomonas aeruginosa, J. Nat. Prod. 59 (3) (1996) 293-296.[8] J.R. Kerr, G.W. Taylor, A. Rutman, N. Hoiby, Pseudomonas aeruginosa pyocyanin and 1-hydroxyphenazine inhibit fungal growth, J. Clin. Pathol. 52 (1999) 385-387.[9] K. Gebhardt, J. Schimana, P. Krastel, K. Dettner, J. Rheinheimer, A. Zeeck, H.P. Fiedler, Endophenazines A similar to D, new phenazine antibiotics from the arthropod associated endosymbiont Streptomyces anulatus I. Taxonomy, fermentation, isolation and biological activities, J. Antibiot. 55 (9) (2002) 794-800.[10] B.S. Yun, I.J. Ryoo, W.G. Kim, J.P. Kim, H. Koshino, H. Seto, I.D. Yoo, Structures of phenazostatins A and B, neuronal cell protecting substances of microbial origin, Tetrahedron Lett. 37 (47) (1996) 8529-8530.[11] S. Mao, S.J. Lee, H. Hwangbo, Y.W. Kim, K.H. Park, G.S. Cha, R.D. Park, K.Y. Kim, Isolation and characterization of antifungal substances from Burkholderia sp. culture broth, Curr. Microbiol. 53 (5) (2006) 358-364.[12] M.S. Abdelfattah, T. Kazufumi, M. Ishibashi, Izumiphenazines A-C: Isolation and structure elucidation of phenazine derivatives from Streptomyces sp. IFM 11204, J. Nat. Prod. 73 (12) (2010) 1999-2002.[13] S. Fotso, D.A. Santosa, R. Saraswati, J. Yang,Modified phenazines from an Indonesian Streptomyces sp. J. Nat. Prod. 73 (3) (2010) 472-475.[14] H.B. Hu, Y.Q. Xu, F. Chen, X.H. Zhang, B.K. Hur, Isolation and characterization of a new fluorescent Pseudomonas strain that produces both phenazine 1-carboxylic acid and pyoluteorin, J. Microbiol. Biotechnol. 15 (2005) 86-90.[15] J.Y. Lee, S.S. Moon, B.K. Hwang, Isolation and in vitro and in vivo activity against Phytophthora capsici and Colletotrichum orbiculare of phenazine-1-carboxylic acid from Pseudomonas aeruginosa strain GC-B26, Pest Manag. Sci. 59 (8) (2003) 872-882.[16] C.A. Whistler, L.S. Pierson, Repression of phenazine antibiotic production in Pseudomonas aureofaciens strain 30-84 by RpeA, J. Bacteriol. 185 (13) (2003) 3718-3725.[17] M.S. Abdelfattah, K. Toume, M. Ishibashi, Izumiphenazine D, a new phenazoquinoline N-oxide from Streptomyces sp. IFM 11204, Chem. Pharm. Bull. 59 (4) (2011) 508-510.[18] I. Zendah, N. Riaz, H. Nasr, H. Frauendorf, A. Schuffler, A. Raies, H. Laatsch, Chromophenazines from the terrestrial Streptomyces sp. Ank 315, J. Nat. Prod. 75 (1) (2012) 2-8.[19] Y. Wang, Q. Luo, X. Zhang, W. Wang, Isolation and purification of a modified phenazine, griseoluteic acid, produced by Streptomyces griseoluteus P510, Res. Microbiol. 162 (3) (2011) 311.[20] P. Masoko, J. Picard, J.N. Eloff, Antifungal activities of six South African Terminalia species (Combretaceae), J. Ethnopharmacol. 99 (2) (2005) 301-308.[21] G. Wheaten, L. Stoel, N. Stevens, C. Frankl, Optical spectra of phenazine, 5, 10- dihydrophenazine, and the phenazhydrins, Appl. Spectrosc. 24 (1970) 339-343.[22] D.V. Mavrodi, R.F. Bonsall, S.M. Delaney, M.J. Soule, Functional analysis of genes for biosynthesis of pyocyanin and phenazine-1-carboxamide from Pseudomonas aeruginosa PAO1, J. Bacteriol. 183 (21) (2001) 6454-6465.[23] A. Raio, G. Puopolo, A. Cimmino, Biocontrol of cypress canker by the phenazine producer Pseudomonas chlororaphis subsp. aureofaciens strain M71, Biol. Control 58 (2) (2011) 133-138.[24] M. Conda-Sheridan, L. Marler, E.J. Park, T.P. Kondratyuk, Potential chemopreventive agents based on the structure of the lead compound 2-bromo-1-hydroxyphenazine, isolated from Streptomyces species, strain CNS284, J. Med. Chem. 53 (24) (2010) 8688-8699.[25] M.R. Rane, P.D. Sarode, B.L. Chaudhari, S.B. Chincholkar, Detection, isolation and identification of phenazine-1-carboxylic acid produced by biocontrol strains of Pseudomonas aeruginosa, J. Sci. Ind. Res. 66 (8) (2007) 627-631.[26] L.S. Thomashow, D.M. Weller, Role of a phenazine antibiotic from Pseudomonas fluorescens in biological control of Gaeumannomyces graminis var. tritici, J. Bacteriol. 170 (8) (1988) 3499-3508.[27] J.R. Kerr, G.W. Taylor, A. Rutman, N. Hoiby, P.J. Cole, R. Wilson, Pseudomonas aeruginosa pyocyanin and 1-hydroxyphenazine inhibit fungal growth, J. Clin. Pathol. 52 (5) (1999) 385-387.[28] J.G. Burgess, K.G. Boyd, E. Armstrong, Z. Jiang, L. Yan, M. Berggren, U. May, D.R. Adams, The development of a marine natural product-based antifouling paint, Biofouling 19 (2003) 197-205.[29] D.V.Mavrodi, V.N. Ksenzeko, R.F. Bonsall, R.J. Cook, A seven-gene locus for synthesis of phenazine-1-carboxylic acid by Pseudomonas fluorescens 2-79, J. Bacteriol. 180 (9) (1998) 2541-2548.[30] S.R. Giddens, Y. Feng, H.K.Mahanty, Characterization of a novel phenazine antibiotic gene cluster in Erwinia herbicola Eh1087, Mol. Microbiol. 45 (3) (2002) 769-783.[31] S.M. Delaney, D.V. Mavrodi, R.F. Bonsall, L.S. Thomashow, phzO, a gene for biosynthesis of 2-hydroxylated phenazine compounds in Pseudomonas aureofaciens 30- 84, J. Bacteriol. 183 (1) (2001) 318-327.[32] T.P. Kondratyuk, E.J. Park, R. Yu, R.B. Van Breemen, R.N. Asolkar, B.T. Murphy, W. Fenical, J.M. Pezzuto, Novelmarine phenazines as potential cancer chemopreventive and anti-inflammatory agents, Mar. Drugs 10 (2) (2012) 451-464.[33] Q.L.Ren,H.B.Xing, Z.B. Bao, B.G. Su,Q.W.Yang, Y.W. Yang, Z.G. Zhang,Recent advances in separation of bioactive natural products, Chin. J. Chem. Eng. 21 (9) (2013) 937-952.[34] S. Imai, K. Furihata, Y. Hayakawa, T. Noguchi, H. Seto, Lavanducyanin, a new antitumor substance produced by Streptomyces sp. J. Antibiot. 42 (1989) 1196-1198.[35] M. Matsumoto, H. Seto, Stimulation ofmammalian cell proliferation by lavanducyanin, J. Antibiot. 44 (1991) 1471-1473. |