Abstract
Endophytes are those inhabiting in plants without causing any apparent loss to the host plant. Phoma is a ubiquitously found genus of fungi in soil, water and air. Endophytic Phoma spp. are distributed with high specific diversity, those occur in plants and are mainly responsible for the production of a vast range of secondary metabolites. These secondary metabolites or the bioactive compounds have demonstrated a wide range of activity ranging from antibacterial, antifungal, antiviral, algicidal, cytotoxic, antitubercular and plant growth promoting, etc. Bioactive compounds are produced by Phoma herbarum, P. sorghina, P. exigua, P. macrostoma, P. medicaginis, P. betae, P. tropica and others. The present review emphasizes on different species of endophytic Phoma as novel source of bioactive compounds, and their applications in medicine and agriculture are documented.
References
- Alvin, A., Miller, K.I., Neilan, B.A. (2014). Exploring the potential of endophytes from medicinal plants as sources of antimycobacterial compounds. Microbiol. Res., 169, 483–495. DOI: 10.1016/j.micres.2013.12.009
- Arora, P., Wani, Z.A., Nalli, Y., Ali A., Hassan, S.R. (2016). Antimicrobial potential of thiodiketopiperazine derivatives produced by Phoma sp., an endophyte of Glycyrrhiza glabra Linn. Microb. Ecol., 72, 802–812. DOI: 10.1007/s00248-016-0805-x
- Aveskamp, M.M., Gruyter, J., de, Crous, P.W. (2008). Biology and recent developments in the systematics of Phoma, a complex genus of major quarantine significance. Fungal. Divers., 31, 1–18.
- Aveskamp, M.M., Gruyter, J., de, Woudenberg, J.H.C., Varkley, G.J.M., Crous, P.W. (2010). Highlights of the Didymellaceae: A polyphasic approach to characterise Phoma and related pleosporalean genera. Stud. Mycol., 65, 1–60. DOI: 10.3114/sim.2010.65.01
- Balmas, V., Scherm, B., Ghignone, S., Salem, A.O.M., Cacciola, S.O., Migheli, Q. (2005). Characterization of Phoma tracheiphila by RAPD-PCR, microsatellite-primed PCR and ITS rDNA sequencing and development of specific primers for in planta PCR detection. European. J. Plant. Pathol., 111, 235–247.
- Bharathidasan, R., Panneerselvam, A. (2011). Isolation and identification of endophytic fungi from Avicennia marina in Ramanathapuram District, Karankadu, Tamilnadu, India. Eur. J. Exper. Biol., 1, 31–36.
- Bick, I.R.C., Rhee, C (1966). Anthraquinone pigments from Phoma foveata Foister. Biochem. J., 98(1), 112–126. DOI: 10.1042/bj0980112
- Boerema, G.H., Gruyter, J., de, Noordeloos, M.E., Hamers, M.E.C. (2004). Phoma identification manual. Differentiation of specific and infra-specific taxa in culture. CABI Publishing, Wallingford, UK.
- Borges, W.D.S., Pupo, M.T. (2006). Novel anthraquinone derivatives produced by Phoma sorghina, an endophyte found in association with the medicinal plant Tithonia diversifolia (Asteraceae). J. Braz. Chem. Soc., 17, 929–934. DOI: 10.1590/S0103-50532006000500017
- Carroll, G. (1988). Fungal endophytes in stems and leaves: from latent pathogen to mutualistic symbiont. Ecology, 69, 2–9.
- Che, Y., Gloer, J.B., Wicklow, D.T. (2002). Phomadecalins A–D and Phomapentenone A: New Bioactive Metabolites from Phoma sp. NRRL 25697, a fungal colonist of Hypoxylon Stromata. J. Nat. Prod., 65, 399–402. DOI: 10.1021/np010519o
- Comby, M., Gacoin, M., Robineau, M., Rabenoelina, F., Ptas, S., Dupont, J., Profizi C., Baillieul, F. (2017). Screening of wheat endophytes as biological control agents against Fusarium head blight using two different in vitro tests. Microbiol. Res., 202, 11–20. DOI: 10.1016/j.micres.2017.04.014
- De Bary, A. (1866). Holfmeister’s Handbook of Physiological Botany, vol. 2. Verlag von Wilhelm Engelmann, Leipzing.
- De Siqueira, V.M., Conti, R., Magali de Araújo, J., Souza-Motta, C.M. (2011). Endophytic fungi from the medicinal plant Lippia sidoides Cham. and their antimicrobial activity. Symbiosis, 53, 89–95. DOI: 10.1007/s13199-011-0113-7
- Eyberger, A.L., Dondapati, R., Porter, J.R. (2006). Endophyte fungal isolates from Podophyllum peltatum produce podophyllotoxin. J. Nat. Prod., 69, 1121–1124.
- Garcia-Effron, G., Park, S., Perlin, D.S. (2009). Correlating echinocandin MIC and kinetic inhibition of fks1 mutant glucan synthases for Candida albicans: implications for interpretive breakpoints. Antimicrob. Agents Chemother., 53, 112–122. DOI: 10.1128/AAC.01162-08
- Ge, H.M., Song, Y.C., Shan, C.Y., Ye, Y.H., Tan, R.X. (2005). New and cytotoxic anthraquinones from Pleospora sp. IFB-E006, an endophytic fungus in Imperata cylindrical. Planta Med., 71, 1063–1065. DOI: 10.1055/s-2005-864190
- Gruyter, J., de, Woudenberg. J.H.C., Aveskamp. M.M., Verkley. G.J.M., Groenewald, J.Z., Crous. P.W. (2010). Systematic reappraisal of species in Phoma section Paraphoma, Pyrenochaeta and Pleuro. Mycologia, 102, 1066–1081. DOI: 10.3852/09-240
- Gruyter, J., de, Aveskamp, M.M., Woudenberg, J.H.C., Verkley, G.J.M., Groenewald, J.Z., Crous, P.W. (2009). Molecular phylogeny of Phoma and allied anamorph genera: Towards a reclassification of the Phoma complex. Mycol. Res., 113, 508–519. DOI: 10.1016/j.mycres.2009.01.002
- Gruyter, J., de, Woudenberg, J.H.C., Aveskamp, M.M., Verkley, G.J.M., Groenewald, J.Z., Crous, P.W. (2012). Redisposition of Phoma-like anamorphs in Pleosporales. Stud. Mycol., 75, 1–36. DOI: 10.3114/sim0004
- Gubiani, J.R., Wijeratne, K., Shi, E.M., Araujo, T., Elizabeth, E.A., Arnold, A., Chapman, E., Gunatilaka, A.A.L. (2017). An epigenetic modifier induces production of (10’S)-verruculide B, an inhibitor of protein tyrosine phosphatases by Phoma sp. nov. LG0217, a fungal endophyte of Parkinsonia microphylla. Bioorg. Med. Chem. DOI: 10.1016/j.bmc.2017.01.048
- Gupta, S., Kaul, S., Singh, B., Vishwakarma, R.A., Dhar, M.K. (2016). Production of Gentisyl Alcohol from Phoma herbarum endophytic in Curcuma longa L. and its antagonistic activity towards leaf spot pathogen Colletotrichum gloeosporioides. Appl. Biochem. Biotechnol., 180, 1093–1109.
- Hamayun, M., Khan, S.A., Khan, A.L., Rehman, G., Sohn, E.Y., Shah, A.A., Kim, S.K., Joo, G.J., Lee, I.J. (2009). Phoma herbarum as a new gibberellin-producing and plant growth-promoting fungus. J. Microbiol. Biotechnol., 19, 1244–1249. DOI: 10.4014/jmb.0901.0030
- Hamzah, T., Lee S., Hidayat, A., Terhem, R., Faridah-Hanum, I., Mohamed, R. (2018). Diversity and characterization of endophytic fungi isolated from the tropical mangrove species, Rhizophora mucronata, and identification of potential antagonists against the soil-borne fungus, Fusarium solani. Front. Microbiol., 9, 1707. DOI: 10.3389/fmicb.2018.01707
- Hensens, O.D., Ondeyka, J.G., Dombrowski, A.W., Ostlind, D.A., Zink D.L. (1999). Isolation and structure of nodulisporic acid A1 and A2, novel insecticides from a Nodulisporium sp. Tetrahedron. Lett., 40, 5455–5458. DOI: 10.1016/S0040-4039(99)01064-3
- Hirsh, G.U., Braun, U. (1992). Communities of parasitic microfungi. In: Handbook of vegetation science: Fungi in vegetation science, Vol. 19, Winterhoff, W. (ed.). Kluwer Academic, Dordrecht, Netherlands, 225–250.
- Hoffman, A.M., Mayer, S.G., Strobel, G.A., Hess W.M., Sovocool, W., Grange, A.H., Kelley-Swift, E.G. (2008). Purification, identification and activity of phomodione, afurandione from an endophytic Phoma species. Phytochemistry, 69, 1049–1056. DOI: 10.1016/j.phytochem.2007.10.031
- Hosseinzadeh, H., Nassiri-Asl, M. (2015). Pharmacological effects of Glycyrrhiza spp. and its bioactive constituents: update and review. Phytother. Res., 29, 1868–1886. DOI: 10.1002/ptr.5487
- Huang, S., Xu, J., Li, F., Zhou, D., Xu, L., Li, C. (2017). Identification and antifungal activity of metabolites from the mangrove fungus Phoma sp. L28. Chem. Nat. Comp., 53, 237–240. DOI: 10.1007/s10600-017-1961-z
- Hynes, R.K. (2018). Phoma macrostoma: as a broad spectrum bioherbicide for turfgrass and agricultural applications. CAB Rev., 13, 005. DOI: 10.1079/PAVSNNR201813005
- Jacob, M., Bhat, D.J. (2000). Two new endophytic conidial fungi from India. Cryptogam. Mycol., 21, 81–88. DOI: 10.1016/S0181-1584(00)00116-0
- Karsten, K., Umar, F., Ulrich, F., Barbara, S., Siegfried, D., Gennaro, P., Piero, S., Sándor, A., Tibor, K. (2007). Secondary metabolites isolated from an endophytic Phoma sp. absolute configuration of tetrahydropyrenophorol using the solid-state TDDFT CD methodology. Eur. J. Org. Chem., 19, 3206–3211. DOI: 10.1002/ejoc.200601128
- Kedar, A., Rathod, D., Yadav, A., Agarkar, G., Rai, M. (2014). Endophytic Phoma sp. isolated from medicinal plants promote the growth of Zea mays. Nusantara Biosci., 6, 132–139. DOI: 10.13057/nusbiosci/n060205
- Khan, A., Gilani, S., Waqas, M., Al-Hosni, K., Al-Khiziri, S., Kim, Y., Ali, L., Kang, S., Asaf, S., Shahzad, R., Hussain, J., Lee I., Al-Harrasi, A. (2017). Endophytes from medicinal plants and their potential for producing indole acetic acid, improving seed germination and mitigating oxidative stress. J. Zhejiang Univ. Sci. B Biomed. Biotechnol., 18, 125–137. DOI: 10.1631/jzus.B1500271
- Khan, R., Shahzad, S., Choudhary, M.I., Khan, S.A., Ahmad, A. (2007). Biodiversity of the endophytic fungi isolated from Calotropis procera (Ait.) R. Br. Pak. J. Bot., 39, 2233–2239.
- Kiprono, P.C., Kaberia, F., Keriko, J.M., Karanja, J.N. (2000). The in vitro anti-fungal and anti-bacterial activities of beta-sitosterol from Senecio lyratus (Asteraceae). Z. Naturforsch. (C), 55, 485–488. DOI: 10.1515/znc-2000-5-629
- Kobayashi, D.Y., Palumbo, J.D. (2000). Bacterial endophytes and their effects on plants and uses in agriculture. In: Microbial Endophytes, Bacon, C.W, White, J.F (eds.). Marcel Dekker, New York, 199–236.
- Koch, C.A., Utkhede, R.S. (2004). Development of a multiplex classical polymerase chain reaction technique for detection of Didymella bryoniae in infected cucumber tissues and greenhouse air samples. Can. J. Plant. Pathol., 26, 291–298. DOI: 10.1080/07060660409507146
- Krohn, K., Farooq, U., Flörke, U., Schulz, B., Draeger, S., Pescitelli, G., Salvadori, P., Antus, S., Kurtán, T. (2007). Secondary metabolites isolated from an endophytic Phoma sp. – Absolute Configuration of Tetrahydropyrenophorol using the solid-state TDDFT CD methodology. Eur. J. Org. Chem., 3206–3211. DOI: 10.1002/ejoc.200601128
- Kumaran, R.S., Choi, Y.K., Lee, S., Jeon, H.J., Jung, H., Kim, H.J. (2014). Isolation of taxol, an anticancer drug produced by the endophytic fungus, Phoma betae. Afr. J. Biotechnol., 11, 950–960. DOI: 10.5897/AJB11.1937
- Kusari, S., Lamshӧft, M., Spiteller, M. (2009a). Aspergillus fumigatus Fresenius, an endophytic fungus from Juniperus communis L. Horstmann as a novel source of the anticancer pro-drug deoxypodophyllotoxin. J. Appl. Microbiol., 107, 1019–1030. DOI: 10.1111/j.1365-2672.2009.04285.x
- Kusari S., Lamshӧft M., Zühlke S., Spiteller M., 2008. An endophytic fungus from Hypericum perforatum that produces hypericin. J. Nat. Prod., 71, 159–162. DOI: 10.1021/np070669k
- Kusari, S., Verma, V.C., Lamsho, ft M., Spiteller, M. (2012). An endophytic fungus from Azadirachta indica A. Juss. that produces azadirachtin. World J. Microbiol. Biotechnol., 28, 1287–1294. DOI: 10.1007/s11274-011-0876-2
- Kusari, S., Zühlke, S., Kosuth, J., Čellárová, E., Spiteller, M. (2009b). Light independent metabolomics of endophytic Thielavia subthermophila provides insight into microbial hypericin biosynthesis. J. Nat. Prod., 72, 1825–1835. DOI: 10.1021/np9002977
- Kusari, S., Zühlke, S., Spiteller, M. (2009c). An endophytic fungus from Camptotheca acuminata that produces camptothecin and analogues. J. Nat. Prod., 72, 2–7. DOI: 10.1021/np800455b
- Larran, S., Simón, M.R., Moreno, M.V., Siurana, M.P.S., Perelló, A. (2016). Endophytes from wheat as biocontrol agents against tan spot disease. Biol. Control., 92, 17–23. DOI: 10.1016/j.biocontrol.2015.09.002
- Lasala, J.M., Stone, G.W., Dawkins, K.D., (2006). An Overview of the TAXUS® Express®, Paclitaxel‐Eluting Stent Clinical Trial Program. J. Interv. Cardiol., 19(5), 422–431. DOI: 10.1111/j.1540-8183.2006.00183.x
- Liu, S.S., Jiang, J.X., Huang, R., Wang, Y.T., Jiang, B.G., Zheng, K.X., Wu, S.H. (2019). A new antiviral 14-nordrimane sesquiterpenoid from an endophytic fungus Phoma sp. Phytochem. Lett., 29, 75–78. DOI: 10.1016/j.phytol.2018.11.005
- Marler, M., Pedersen, D., Mitchell-Olds, T., Callaway, R.M. (1999). A polymerase chain reaction method for detecting dwarf mistletoe infection in Douglas-fir and western larch. Can. J. For. Res., 29, 1317–1321. DOI: 10.1139/x99-092
- Martinez-Klimova, E., Rodríguez-Peña, K., Sánchez, S. (2017). Endophytes as sources of antibiotics. Biochem. Pharmacol., 134, 1–17. DOI: 10.1016/j.bcp.2016.10.010
- Melmed, R.N., Ishai-Michaeli, R., Yagen, B. (1985). Differential inhibition by T-2 toxin of total protein, DNA and isoprenoid synthesis in the culture macrophage cell line J744. Biochem. Pharmacol., 34, 2809–2812. DOI: 10.1016/0006-2952(85)90583-0
- Michael, A.C., Mierzwa, R., King ,A., Loebenverg, D., Bishop, W.R., Puar, M., Patel, M., Coval, S.J., Hershenhorn, J., Strobel, G.A. (1992). Usnic acid amide, a phytotoxin and antifungal agent from Cercosporidium henningsii. Phytochemistry, 31, 2999–3001. DOI: 10.1016/0031-9422(92)83434-Z
- Monte, E., Bridge, P.D., Sutton, B.C. (1991). An integrated approach to Phoma systematics. Mycopathologia, 115, 89–103.
- Moster, L., Crous P.W., Petrini O. (2000). Endophytic fungi associated with shoots and leaves of Vitis vinifera, and specific reference to the Phomopsis viticola complex. Sydowia, 52, 46–58.
- Muhammad, H., Khan, S.A., Khan, A.L., Rehman, G., Sohn, E.Y., Shah, A.A., Kim, S.K., Joo, G.J., Lee, I.J. (2009). Phoma herbarum as a new gibberellin-producing and plant growth-promoting fungus. J. Microbiol. Biotechnol., 19, 1244–1249. DOI: 10.4014/jmb.0901.0030
- Nisa, H., Kamili, A.N., Nawchoo, A.I., Shafi, S., Shameem, N., Bandh, S.A. (2015). Fungal endophytes as prolific source of phytochemicals and other bioactive natural products: A review. Microb. Pathog., DOI: 10.1016/j.micpath.2015.04.001
- Oberlie, N.H., Kroll, D.J. (2004). Camptothecin and taxol: historic achievements in natural products research. J. Nat. Prod., 67, 129–35. DOI: 10.1021/np030498t
- Osterhage, C., Konig, G.M., Jones, P.G., Wright, A.D. (2002). 5-Hydroxyramulosin, a new natural product produced by Phoma tropica, a marine derived fungus derived from alg Fucus spiralis. Plant. Med., 68, 1052–1054. DOI: 10.1055/s-2002-35670
- Osterhage, C., Schwibibble, M., Konig, G.M., Wright, A.D. (2000). Differences between marine amnd terrestrial Phoma species as determined by HPLC-DAD and HPLC-MS. Phytochem. Anal., 11, 288–294. DOI: 10.1002/1099-1565(200009/10)11:5%3C288::AID-PCA528%3E3.0.CO;2-G
- Paynter, Q., Waipara, N., Peterson, P., Hona, S., Fowler, S., Gianotti, A., Wilkie, P. (2006). The impact of two introduced biocontrol agents, Phytomyza vitalbae and Phoma clematidina, on Clematis vitalba in New Zealand. Biol. Control., 36, 350–357. DOI: 10.1016/j.biocontrol.2005.09.011
- Petrini, O. (1991). Fungal endophytes of tree leaves. In: Microbial Ecology of Leaves, Andrews, J., Hirano, S. (eds.), 179–197. Springer Verlag, New York–Berlin–Heidelberg–London–Paris–Tokyo–Hong Kong–Barcelona–Budapest.
- Pharamat, T., Palaga, T., Piapukiew, J., Whalley, A.J.S., Sihanonth, P. (2013). Antimicrobial and anticancer activities of endophytic fungi from Mitrajyna javanica Koord and Val. Afr. J. Microbiol. Res., 7, 5565–5572. DOI: 10.5897/AJMR12.2352
- Puri, S.C., Verma, V., Amna, T., Qazi, G.N., Spiteller, M. (2005). An endophytic fungus from Nothapodytes foetida that produces camptothecin. J. Nat. Prod., 68, 1717–1719. DOI: 10.1021/np0502802
- Qin, S., Hussaina, H., Schulz, B., Draeger, S., Krohn, K. (2010). Two New Metabolites, Epoxydine A and B, from Phoma sp., Helv. Chim. Acta, 93(1), 19–174. DOI: 10.1002/hlca.200900199
- Rai, M., Agarkar, G. (2015). Plant-fungal interactions: What triggers the fungi to switch among lifestyles? Crit. Rev. Microbiol., 42, 428–438. DOI: 10.3109/1040841X.2014.958052
- Rai, M., Gade, A., Zimowska, B., Ingle, A.P., Ingle, P. (2018). Marine-derived Phoma-the gold mine of bioactive compounds. Appl. Microbiol. Biotechnol., 102 , 9053–9066. DOI: 10.1007/s00253-018-9329-2
- Rai, M., Rathod, D., Agarkar, G., Dar, M., Brestic, M., Marostica Junior, M.R. (2014). Fungal growth promotor endophytes: a pragmatic approach towards sustainable food and agriculture. Symbiosis, 62, 63–79. DOI: 10.1007/s13199-014-0273-3
- Rai, M., Rathod, D., Ingle, A., Proksch, P., Kon, K., (2013). Biocidal Metabolites from Endophytes Occurring in Medicinal Plants. In: Natural Antioxidants and Biocides from Wild Medicinal Plants, Cespedes, C., Sampietro, D., Rai, M., Seigler, D. (eds.). CABI, U.K., 56–64.
- Rebecca, I.N.A., Kumar, D.J.M., Srimathi, S., Muthumary, J., Kalaichelvan, P.T. (2011). Isolation of Phoma species from Aloe vera: an endophyte and screening the fungus for taxol production. World. J. Sci. Technol., 1, 23–31.
- Saikkonen, K., Faeth, S.H., Helander, M., Sullivan, T.J. (1998). Fungal endophytes: a continuum of interactions with host plants. Annu. Rev. Ecol. Syst., 29, 319–343.
- Santiago, C., Fitchett, C., Munro, M.H.G., Jalil, J., Santhanam, J. (2012). Cytotoxic and antifungal activities of 5-hydroxyramulosin, a compound produced by an endophytic fungus isolated from Cinnamomum mollisimum. Evid.-Based Complement. Altern. Med., Article ID 689310. DOI: 10.1155/2012/689310
- Schardl, C.L., Liu, J.S., White, J.F., Finkel, R.A., An Z., Siegel, M.R. (1991). Molecular phylogenetic relationships of nonpathogenic grass mycosymbionts and clavicipitaceous plant pathogens. Plant. Syst. Evol., 178, 27–41.
- Schulz, B., Boyle, C. (2005). The endophyte continuum. Mycol. Res., 109, 661–689. PMID: 16080390.
- Shweta, S., Zuehlke, S., Ramesha, B.T., Priti, V., Mohana Kumar, P., Ravikanth, G., Spiteller, M., Vasudeva, R., Uma Shaanker, R. (2010). Endophytic fungal strains of Fusarium solani, from Apodytes dimidiate E. Mey. ex Arn (Icacinaceae) produce camptothecin, 10-hydroxycamptothecin and 9-methoxycamptothecin. Phytochemistry, 71, 117–122. DOI: 10.1016/j.phytochem.2009.09.030
- Stewart-Wade, S.M., Boland, G.J. (2005). Oil emulsions increase efficacy of Phoma herbarum to control dandelion but are phytotoxic. Biocontrol. Sci. Technol., 15, 671–681. DOI: 10.1080/09583150500136873
- Stierle, A., Strobel, G.A., Stierle, D. (1993). Taxol and taxane production by Taxomyces andreanae, an endophytic fungus of Pacific yew. Science, 260, 214–216.
- Stone, J.K., Bacon, C.W., White, J.F. (2000). An overview of endophytic microbes:endophytism defined. In: Microbial Endophytes, Bacon, C.W, White, J.F (eds.). Marcel Dekker, New York, pp. 3–30.
- Strobel, G., Daisy, B. (2003). Bioprospecting for microbial endophytes and their natural products. Microbiol. Mol. Biol. Rev., 67, 491–502.
- Strobel, G., Daisy, B., Castillo, U., Harper, J. (2004). Natural products from endophytic microorganisms. J. Nat. Prod., 67, 257–68.
- Strobel, G., Knighton, B., Kluck, K., Ren, Y., Livinghouse, T., Griffen, M., Spakowicz, D., Sears, J. (2008). The production of myco-diesel hydrocarbons and their derivatives by the endophytic fungus Gliocladium roseum. Microbiology, 154, 3319–3328. DOI: 10.1099/mic.0.30824-0
- Strobel, G., Singh, S.K., Riyaz-Ul-Hassan, S., Mitchell, A.M., Geary, B., Sears, J. (2011). An endophytic/pathogenic Phoma sp. from creosote bush producing biologically active volatile compounds having fuel potential. FEMS Microbiol. Lett. 320, 87–94. DOI: 10.1111/j.1574-6968.2011.02297.x
- Strobel, G.A. (2002). Microbial gifts from the rainforest. Can. J. Phytopathol. 24, 14–20.
- Suryanarayanan, T.S., Murali, T.S., Venkatesan, G. (2002). Occurrence and distribution of fungal endophytes in tropical forests across a rainfall gradient. Can. J. Bot., 80, 818–826. DOI: 10.1139/b02-069
- Tijerino, A., Cardoza, R.E., Moraga, J., Malmierca, M.G., Vicente, F., Aleu, J., Collado, I.G., Gutiérrez, S., Monte, E., Hermos, R. (2011). Overexpression of the trichodiene synthase gene tri5 increases trichodermin production and antimicrobial activity in Trichoderma brevicompactum. Fungal. Genet. Biol., 48, 285–296. DOI: 10.1016/j.fgb.2010.11.012
- Tooker, J.F., Hanks, L.M. (2004). Trophic position of the endophytic beetle, Mordellistena aethiops Smith (Coleoptera: Mordellidae). Environ. Entomol., 33, 291–296. DOI: 10.1603/0046-225X-33.2.291
- Trémouillaux-Guiller, J., Rohr, T., Rohr, R., Huss, V.A.R. (2002). Discovery of an endophytic alga in Ginkgo biloba. Am. J. Bot., 89, 727–733.
- Vieira, M.L., Hughes, A.F., Gil, V.B., Vaz, A.B., Alves, T.M., Zani, C.L., Rosa, C.A., Rosa, L.H. (2012). Diversity and antimicrobial activities of the fungal endophyte community associated with the traditional Brazilian medicinal plant Solanum cernuum Vell. (Solanaceae). Can. J. Microbiol., 58, 54–66. DOI: 10.1139/W11-105
- Vries, S., de, Dahlen, J.K., von, Schnake, A., Ginschel, S., Schulz, B., Rose, L.E. (2018). Broad-spectrum inhibition of Phytophthora infestans by fungal endophytes. FEMS Microbiol. Ecol., 94(4), fiy 037. DOI: 10.1093/femsec/fiy037
- Wang, L.W., Xu, B.G., Wang, J.Y., Su, Z.Z., Lin, F.C., Zhang, C.L., Kubicek, C.P. (2012). Bioactive metabolites from Phoma species, an endophytic fungus from the Chinese medicinal plant Arisaema erubescens. Appl. Microbiol. Biotechnol., 93, 1231–1239. DOI: 10.1007/s00253-011-3472-3
- Waqas, M., Khan, A.L., Hamayun, M., Kamran, M., Kang, S.M., Kim, Y.H., Lee, I.J. (2012a). Assessment of endophytic fungi cultural filtrate on soybean seed germination. Afr. J. Biotechnol., 11, 15135–15143.
- Waqas, M., Khan, A.L., Kamran, M., Hamayun, M., Kang, S.M., Kim, Y.H., Lee, I.J. (2012b). Endophytic fungi produce gibberellins and indole-acetic acid and promotes host-plant growth during stress. Molecules, 17, 10754–10773. DOI: 10.3390/molecules170910754
- Weber, R.W.S., Stenger, E., Meffert, A., Hahn, M. (2004). Brefeldin A production by Phoma medicaginis in dead pre-colonized plant tissue: a strategy for habitat conquest? Mycol. Res., 108, 662–671. DOI: 10.1017/S0953756204000243
- Wilson, D. (1995). Endophyte – the evolution of the term, a clarification of its use and definition. Oikos, 73, 274–276.
- Wink, M. (2008). Plant secondary metabolism: diversity, function and its evolution. Nat. Prod. Commun., 3, 1205–1216.
- Wijeratne, E.K., He, H., Franzblau, S.G., Hoffman, A.M., Gunatilaka, A.L. (2013). Phomapyrrolidones A–C, antitubercular alkaloids from the endophytic fungus Phoma sp. NRRL 46751. J. Nat. Prod., 76(10), 1860–1865. DOI: 10.1021/np400391p
- Xia, X., Kim, S., Bang, S., Lee, H.J., Liu, C., Park, C.I., Shim, S.H. (2014). Barceloneic acid C, a new polyketide from an endophytic fungus Phoma sp. JS752 and its antibacterial activities. J. Antibiot., 1–3. DOI: 10.1038/ja.2014.116
- Yang, X., Strobel, G., Stierle, A., Hess, W.M., Lee, J., Clardy, J. (1994). A fungal endophyte-tree relationship: Phoma sp. in Taxus wallachiana. Plant Sci., 102, 1–9. DOI: 10.1016/0168-9452(94)90017-5
- Yarden, O., Ainsworth, T.D., Roff, G., Leggat, W., Fine, M., Hoegh-Guldberg, O. (2007). Increased prefalence of ubiquitous ascomycetes in an acropoid coral (Acropora formosa) exibiting symptoms of brown band syndrome and skeletal eroding band disease. Appl. Env. Microbiol., 73, 2755–2757. DOI: 10.1128/AEM.02738-06
- Zaiyou, J., Li, M., Xiqiao, H. (2017). An endophytic fungus efficiently producing paclitaxel isolated from Taxus wallichiana var. mairei. Medicine, 96, 27(e7406). DOI: 10.1097/MD.0000000000007406
- Zakaria, L., Aziz, W.N.W. (2018). Molecular identification of endophytic fungi from banana leaves (Musa spp.). Tropical. Life. Sci. Res., 29, 201–211. DOI: 10.21315/tlsr2018.29.2.14
- Zhang, L., Wang, S.Q., Li X.J., Zhang, A.L., Zhang, Q., Gao, J.M. (2012). New insight into the stereochemistry of botryosphaeridione from a Phoma endophyte. J. Mol. Struct., 1016, 72–75. DOI: 10.1016/j.molstruc.2012.02.041
- Zhang, W., Krohn, K., Egold, H., Draeger, S., Schulz, B. (2008). Diversity of antimicrobial pyrenophorol derivatives from an endophytic fungus, Phoma sp. Eur. J. Organic. Chem., 25, 4320–4328. DOI: 10.1002/ejoc.200800404
- Zhao, S., Shamoun, S.F. (2006). Effects of cultre media, temperature, pH, and light on growth, sporulation, germination, and bioherbicidal efficacy of Phoma exigua, a potential biological control agent for salal (Gaultheria shallon). Biocontrol. Sci. Technol., 16, 1043–1055. DOI: 10.1080/09583150600828643
- Zhou, L., Bailey, K.L., Derby, J. (2004). Plant colonization and environmental fate of the biocontrol fungus Phoma macrostoma. Biol. Control., 30, 634–644. DOI: 10.1016/j.biocontrol.2004.03.002
Downloads
Download data is not yet available.
-
Sebnem Kusvuran,
H. Yildiz Dasgan,
DROUGHT INDUCED PHYSIOLOGICAL AND BIOCHEMICAL RESPONSES IN Solanum lycopersicum GENOTYPES DIFFERING TO TOLERANCE
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 16 No. 6 (2017)
-
Agata Goryluk-Salmonowicz,
Aleksandra Orzeszko-Rywka,
Monika Piórek,
Hanna Rekosz-Burlaga,
Adrianna Otłowska Otłowska,
Dariusz Gozdowski,
Mieczysław Błaszczyk,
PLANT GROWTH PROMOTING BACTERIAL ENDOPHYTES ISOLATED FROM POLISH HERBAL PLANTS
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 17 No. 5 (2018)
-
Yasin Ozdemir,
Mehmet Emin Akcay,
Sezai Ercisli,
Mehmet Ozkan,
Ugur Ozyurt,
PHYSICAL, CHEMICAL, SENSORIAL AND BIOACTIVE CHARACTERISTICS OF LOCAL AND STANDARD PEAR CULTIVARS IN TURKEY
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 15 No. 3 (2016)
-
Burhan Ozturk,
Orhan Karakaya,
Suleyman Muhammed Celik,
Medeni Karakaya,
Saadet Koc Guler,
Tarık Yarılgac,
Habip Aydın,
Ahmet Ozturk,
THE EFFECT OF COLD STORAGE ON THE BIOACTIVE COMPONENTS AND PHYSICAL PROPERTIES OF CAUCASIAN WHORTLEBERRY (Vaccinium arctostaphylos L.). A PRELIMINARY STUDY
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 15 No. 2 (2016)
-
Urszula Gawlik-Dziki,
Michał Świeca,
Danuta Sugier,
ENHANCEMENT OF ANTIOXIDANT ABILITIES AND THE LIPOXYGENASE AND XANTHINE OXIDASE INHIBITORY ACTIVITY OF BROCCOLI SPROUTS BY BIOTIC ELICITORS
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 11 No. 1 (2012)
-
Monika Kordowska-Wiater,
Anna Wagner,
Beata Hetman,
EFFICACY OF Candida melibiosica FOR CONTROL OF POST-HARVEST FUNGAL DISEASES OF CARROT (Daucus carota L.)
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 11 No. 5 (2012)
-
Mariola Kozłowska,
Agnieszka E. Laudy,
Bohdan J. Starościak,
Artur Napiórkowski,
Lidia Chomicz,
Zygmunt Kazimierczuk,
ANTIMICROBIAL AND ANTIPROTOZOAL EFFECT OF SWEET MARJORAM (Origanum majorana L.)
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 9 No. 4 (2010)
-
Barbara Łata,
Aleksandra Trąmpczyńska,
RELATIONSHIP BETWEEN APPLE BIOACTIVE COMPOUNDS AFTER HARVEST AND THEIR FATE IN COLD STORED FRUITS
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 7 No. 2 (2008)
-
Memnune Sengul,
Derya Sener,
Sezai Ercisli,
THE DETERMINATION OF ANTIOXIDANT CAPACITIES AND CHEMICAL PROPERTIES OF ROSA (Rosa damascena Mill.) PRODUCTS
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 16 No. 4 (2017)
-
Urszula Gawlik-Dziki,
Michał Świeca,
Danuta Sugier,
Joanna Cichocka,
COMPARISON OF in vitro LIPOXYGENASE, XANTHINE OXIDASE INHIBITORY AND ANTIOXIDANT ACTIVITY OF Arnica montana AND Arnica chamissonis TINCTURES
,
Acta Scientiarum Polonorum Hortorum Cultus: Vol. 10 No. 3 (2011)
<< < 7 8 9 10 11 12 13 14 15 16 > >>
You may also start an advanced similarity search for this article.