O-Methylmellein

O-Methylmellein

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O-Methylmellein
Category Others
Catalog number BBF-05577
CAS 76985-75-6
Molecular Weight 192.21
Molecular Formula C11H12O3

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Description

It is the constituent of Septoria nodorum.

Specification

Synonyms 1H-2-Benzopyran-1-one, 3,4-dihydro-8-methoxy-3-methyl-, (3R)-; (R)-O-Methylmellein; (R)-8-methoxy-3-methylisochroman-1-one; (3R)-8-Methoxy-3-methyl-3,4-dihydro-1H-isochromen-1-one; (3R)-O-Methylmellein
IUPAC Name (3R)-8-methoxy-3-methyl-3,4-dihydroisochromen-1-one
Canonical SMILES CC1CC2=C(C(=CC=C2)OC)C(=O)O1
InChI InChI=1S/C11H12O3/c1-7-6-8-4-3-5-9(13-2)10(8)11(12)14-7/h3-5,7H,6H2,1-2H3/t7-/m1/s1
InChI Key AYIDXPPINFIJKW-SSDOTTSWSA-N

Properties

Appearance Crystal
Boiling Point 373.5±42.0°C at 760 mmHg
Melting Point 88-89°C
Density 1.1±0.1 g/cm3

Reference Reading

1. Dynamics of Metabolite Induction in Fungal Co-cultures by Metabolomics at Both Volatile and Non-volatile Levels
Antonio Azzollini, Lorenzo Boggia, Julien Boccard, Barbara Sgorbini, Nicole Lecoultre, Pierre-Marie Allard, Patrizia Rubiolo, Serge Rudaz, Katia Gindro, Carlo Bicchi, Jean-Luc Wolfender Front Microbiol. 2018 Feb 5;9:72. doi: 10.3389/fmicb.2018.00072. eCollection 2018.
Fungal co-cultivation has emerged as a promising way for activating cryptic biosynthetic pathways and discovering novel antimicrobial metabolites. For the success of such studies, a key element remains the development of standardized co-cultivation methods compatible with high-throughput analytical procedures. To efficiently highlight induction processes, it is crucial to acquire a holistic view of intermicrobial communication at the molecular level. To tackle this issue, a strategy was developed based on the miniaturization of fungal cultures that allows for a concomitant survey of induction phenomena in volatile and non-volatile metabolomes. Fungi were directly grown in vials, and each sample was profiled by head space solid phase microextraction gas chromatography mass spectrometry (HS-SPME-GC-MS), while the corresponding solid culture medium was analyzed by liquid chromatography high resolution mass spectrometry (LC-HRMS) after solvent extraction. This strategy was implemented for the screening of volatile and non-volatile metabolite inductions in an ecologically relevant fungal co-culture of Eutypa lata (Pers.) Tul. & C. Tul. (Diatrypaceae) and Botryosphaeria obtusa (Schwein.) Shoemaker (Botryosphaeriaceae), two wood-decaying fungi interacting in the context of esca disease of grapevine. For a comprehensive evaluation of the results, a multivariate data analysis combining Analysis of Variance and Partial Least Squares approaches, namely AMOPLS, was used to explore the complex LC-HRMS and GC-MS datasets and highlight dynamically induced compounds. A time-series study was carried out over 9 days, showing characteristic metabolite induction patterns in both volatile and non-volatile dimensions. Relevant links between the dynamics of expression of specific metabolite production were observed. In addition, the antifungal activity of 2-nonanone, a metabolite incrementally produced over time in the volatile fraction, was assessed against Eutypa lata and Botryosphaeria obtusa in an adapted bioassay set for volatile compounds. This compound has shown antifungal activity on both fungi and was found to be co-expressed with a known antifungal compound, O-methylmellein, induced in solid media. This strategy could help elucidate microbial inter- and intra-species cross-talk at various levels. Moreover, it supports the study of concerted defense/communication mechanisms for efficiently identifying original antimicrobials.
2. Ruthenium-NHC-Diamine Catalyzed Enantioselective Hydrogenation of Isocoumarins
Wei Li, Mario P Wiesenfeldt, Frank Glorius J Am Chem Soc. 2017 Feb 22;139(7):2585-2588. doi: 10.1021/jacs.6b13124. Epub 2017 Feb 8.
A novel and practical chiral ruthenium-NHC-diamine system is disclosed for the enantioselective hydrogenation of isocoumarins, which provides a new concept to apply (chiral) NHC ligands in asymmetric catalysis. A variety of optically active 3-substituted 3,4-dihydroisocoumarins were obtained in excellent enantioselectivities (up to 99% ee). Moreover, this methodology was utilized in the synthesis of O-methylmellein, mellein, and ochratoxin A.
3. Hunting modulators of plant defence: the grapevine trunk disease fungus Eutypa lata secretes an amplifier for plant basal immunity
Pingyin Guan, Florian Schmidt, Michael Riemann, Jochen Fischer, Eckhard Thines, Peter Nick J Exp Bot. 2020 Jun 22;71(12):3710-3724. doi: 10.1093/jxb/eraa152.
Grapevine trunk diseases (GTDs) are progressively affecting vineyard longevity and productivity worldwide. To be able to understand and combat these diseases, we need a different concept of the signals exchanged between the grapevine and fungi than the well-studied pathogen-associated molecular pattern and effector concepts. We screened extracts from fungi associated with GTDs for their association with basal defence responses in suspension cells of grapevine. By activity-guided fractionation of the two selected extracts, O-methylmellein was identified as a candidate modulator of grapevine immunity. O-Methylmellein could not induce immune responses by itself (i.e. does not act as an elicitor), but could amplify some of the defence responses triggered by the bacterial elicitor flg22, such as the induction level of defence genes and actin remodelling. These findings show that Eutypa lata, exemplarily selected as an endophytic fungus linked with GTDs, can secrete compounds that act as amplifiers of basal immunity. Thus, in addition to elicitors that can trigger basal immunity, and effectors that down-modulate antibacterial basal immunity, once it had been activated, E. lata seems to secrete a third type of chemical signal that amplifies basal immunity and may play a role in the context of consortia of mutually competing microorganisms.

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