Mycol Res 110:1257–1270PubMedCrossRef Tringe SG, Hugenholtz P (20

Mycol Res 110:1257–1270PubMedCrossRef Tringe SG, Hugenholtz P (2008) A renaissance for the pioneering 16S rRNA gene. Curr Opin Microbiol 11:442–446PubMedCrossRef Vega FE, Posada F, Peterson SW, Gianfagna TJ, Chaves F (2006) Penicillium species endophytic in coffee plants and ochratoxin A production. Mycologia 98:31–42PubMedCrossRef Vilgalys R, Hester M (1990) Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species. J Bacteriol 172:4238–4246PubMedPubMedCentral

Wakelin S, Gupta VV, Harvey P, Ryder M (2007) The effect of Penicillium fungi on plant growth and phosphorus mobilization in neutral to alkaline soils from southern Australia. Can J Microbiol 53:106–115PubMedCrossRef Napabucasin concentration Wang Y-T (2004) Flourishing market for potted orchids. FlowerTech 7:2–5 Wey G (1988) Occurrence

and investigation of important diseases on Phalaenopsis in Taiwan. Rep Taiwan Sugar Res Inst 122:31–41 Wu Z, Wang X-R, Blomquist G (2002) Evaluation of PCR primers and PCR conditions for specific detection of common airborne fungi. J Environ Monitor 4:377–382CrossRef Wu P-H, Huang D-D, Chang DCN (2011) Mycorrhizal symbiosis enhances Phalaenopsis orchid’s growth and resistence to Erwinia chrysanthemi. Afr J Biotechnol 10:10095–10100CrossRef selleck compound Yang Y, Cai L, Yu Z, Liu Z, Hyde KD (2011) Colletotrichum species on Orchidaceae in southwest China. Cryptogam Mycol 32:229–253CrossRef Zelmer CD, Cuthbertson L, Currah RS (1996) Fungi associated with many terrestrial orchid mycorrhizas, seeds and protocorms. Mycoscience 37:439–448CrossRef Zeng QY, Rasmuson-Lestander Å, Wang XR (2004) Extensive set of mitochondrial LSU rDNA‐based oligonucleotide probes for the detection of common airborne fungi. FEMS Microb Lett 237:79–87CrossRef Zhang X, Andrews JH (1993) Evidence for growth of Sporothrix schenckii on dead but not on living Sphagnum moss. Mycopathologia 123:87–94PubMedCrossRef”
“Introduction Currently, the

fungal genus Trichoderma/Hypocrea 1 comprises more than 200 validly described species, which have been recognised by molecular phylogenetic analysis (Atanasova et al. 2013). This high taxonomic diversity in Trichoderma/Hypocrea is not only reflected in a permanently increasing number of species (Jaklitsch 2009, 2011; Jaklitsch and Voglmayr 2012; Jaklitsch et al. 2012, 2013; Chaverri et al. 2011; Samuels and Ismaiel 2011, Samuels et al. 2012a,b; Kim et al. 2012, 2013; Yamaguchi et al. 2012; Li et al. 2013; López-Quintero et al. 2013, Yabuki et al. 2014), but also in a fast-growing number of secondary metabolites of remarkable structural diversity. The latter include low-molecular-weight Palbociclib chemical structure compounds such as pyrones (Jeleń et al. 2013), butenolides, terpenes, and steroids, but also N-heterocyclic compounds and isocyanides.

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