Pyrenophoric acid, a phytotoxic sesquiterpenoid penta-2,4-dienoic acid produced by a potential mycoherbicide, Pyrenophora semeniperda.

A new phytotoxic sesquiterpenoid penta-2,4-dienoic acid, named pyrenophoric acid, was isolated from solid wheat seed culture of Pyrenophora semeniperda, a fungal pathogen proposed as a mycoherbicide for biocontrol of cheatgrass (Bromus tectorum) and other annual bromes. These bromes are serious weeds in winter cereals and also on temperate semiarid rangelands. Pyrenophoric acid was characterized as (2Z,4E)-5-[(7S,9S,10R,12R)-3,4-dihydroxy-2,2,6-trimethylcyclohexyl)]-3-methylpenta-2,4-dienoic acid by spectroscopic and chemical methods. The relative stereochemistry of pyrenophoric acid was assigned using 1H,1H couplings and NOESY experiments, while its absolute configuration was determined by applying the advanced Mosher's method. Pyrenophoric acid is structurally quite closely related to the plant growth regulator abscisic acid. When bioassayed in a cheatgrass coleoptile elongation test at 10(-3) M, pyrenophoric acid showed strong phytotoxicity, reducing coleoptile elongation by 51% relative to the control. In a mixture at 10(-4) M, its negative effect on coleoptile elongation was additive with that of cytochalasin B, another phytotoxic compound found in the wheat seed culture extract of this fungus, demonstrating that the extract toxicity observed in earlier studies was due to the combined action of multiple phytotoxic compounds.

[1]  A. Cimmino,et al.  Phytotoxic Terpenes Produced by Phytopathogenic Fungi and Allelopathic Plants , 2014, Natural product communications.

[2]  A. Cimmino,et al.  Spirostaphylotrichin W, a spirocyclic γ-lactam isolated from liquid culture of Pyrenophora semeniperda, a potential mycoherbicide for cheatgrass (Bromus tectorum) biocontrol , 2014 .

[3]  M. Masi,et al.  Effect of strain and cultural conditions on the production of cytochalasin B by the potential mycoherbicide Pyrenophora semeniperda (Pleosporaceae, Pleosporales) , 2014 .

[4]  T. Asami,et al.  Chemical biology of abscisic acid , 2011, Journal of Plant Research.

[5]  W. Hartung The evolution of abscisic acid (ABA) and ABA function in lower plants, fungi and lichen , 2010 .

[6]  J. Barnes Medicinal natural products , 2010 .

[7]  Wei Zhang,et al.  Gynostemosides A-E, megastigmane glycosides from Gynostemma pentaphyllum. , 2010, Phytochemistry.

[8]  A. Osbourn,et al.  Plant-derived Natural Products , 2009 .

[9]  S. Abrams,et al.  Chemistry of Abscisic Acid, Abscisic Acid Catabolites and Analogs , 2005, Journal of Plant Growth Regulation.

[10]  S. Berger,et al.  200 and More NMR Experiments: A Practical Course , 2004 .

[11]  D. Richardson,et al.  Effects of Invasive Alien Plants on Fire Regimes , 2004 .

[12]  H. Kikuzaki,et al.  Abscisic acid related compounds and lignans in prunes (Prunus domestica L.) and their oxygen radical absorbance capacity (ORAC). , 2004, Journal of agricultural and food chemistry.

[13]  H. Ohigashi,et al.  Biosynthesis of Abscisic Acid by the Direct Pathway via Ionylideneethane in a Fungus, Cercospora cruenta , 2004, Bioscience, biotechnology, and biochemistry.

[14]  T. Oritani,et al.  Biosynthesis and metabolism of abscisic acid and related compounds. , 2003, Natural product reports.

[15]  A. Evidente,et al.  Cytochalasins Z1, Z2 and Z3, three 24-oxa[14]cytochalasans produced by Pyrenophora semeniperda. , 2002, Phytochemistry.

[16]  L. Walker,et al.  Biologically active secondary metabolites from Ginkgo biloba. , 2002, Journal of agricultural and food chemistry.

[17]  H. Kalinowski,et al.  150 and More Basic NMR Experiments: A Practical Course , 1996 .

[18]  Stephen D. Miller,et al.  Downy Brome (Bromus tectorum) Interference and Economic Thresholds in Winter Wheat (Triticum aestivum) , 1990, Weed Science.

[19]  T. Kusumi,et al.  Absolute configurations of marine diterpenes possessing a xenicane skeleton. An application of an advanced mosher's method , 1989 .

[20]  D. C. Aldridge,et al.  Fungal metabolites II , 1983 .

[21]  E. Breitmaier,et al.  [Carbon 13 NMR spectroscopy]. , 1976, Pharmazie in unserer Zeit.

[22]  R. Schultz,et al.  Infrared absorption spectroscopy. , 1971, American Industrial Hygiene Association journal.

[23]  D. Walton,et al.  Structure-activity correlations with compounds related to abscisic acid. , 1970, Plant physiology.

[24]  S. Sternhell Correlation of interproton spin–spin coupling constants with structure , 1969 .

[25]  A. Scott Interpretation of the ultraviolet spectra of natural products , 1964 .