isopimaric-acid and abietic-acid

isopimaric-acid has been researched along with abietic-acid* in 5 studies

Other Studies

5 other study(ies) available for isopimaric-acid and abietic-acid

ArticleYear
Modularity of Conifer Diterpene Resin Acid Biosynthesis: P450 Enzymes of Different CYP720B Clades Use Alternative Substrates and Converge on the Same Products.
    Plant physiology, 2016, Volume: 171, Issue:1

    Cytochrome P450 enzymes of the CYP720B subfamily play a central role in the biosynthesis of diterpene resin acids (DRAs), which are a major component of the conifer oleoresin defense system. CYP720Bs exist in families of up to a dozen different members in conifer genomes and fall into four different clades (I-IV). Only two CYP720B members, loblolly pine (Pinus taeda) PtCYP720B1 and Sitka spruce (Picea sitchensis) PsCYP720B4, have been characterized previously. Both are multisubstrate and multifunctional clade III enzymes, which catalyze consecutive three-step oxidations in the conversion of diterpene olefins to DRAs. These reactions resemble the sequential diterpene oxidations affording ent-kaurenoic acid from ent-kaurene in gibberellin biosynthesis. Here, we functionally characterized the CYP720B clade I enzymes CYP720B2 and CYP720B12 in three different conifer species, Sitka spruce, lodgepole pine (Pinus contorta), and jack pine (Pinus banksiana), and compared their activities with those of the clade III enzymes CYP720B1 and CYP720B4 of the same species. Unlike the clade III enzymes, clade I enzymes were ultimately found not to be active with diterpene olefins but converted the recently discovered, unstable diterpene synthase product 13-hydroxy-8(14)-abietene. Through alternative routes, CYP720B enzymes of both clades produce some of the same profiles of conifer oleoresin DRAs (abietic acid, neoabietic acid, levopimaric acid, and palustric acid), while clade III enzymes also function in the formation of pimaric acid, isopimaric acid, and sandaracopimaric acid. These results highlight the modularity of the specialized (i.e. secondary) diterpene metabolism, which produces conifer defense metabolites through variable combinations of different diterpene synthase and CYP720B enzymes.

    Topics: Abietanes; Amino Acid Sequence; Base Sequence; Carboxylic Acids; Cloning, Molecular; Cytochrome P-450 Enzyme System; Diterpenes; Diterpenes, Kaurane; DNA, Complementary; DNA, Plant; Escherichia coli; Gas Chromatography-Mass Spectrometry; Gene Expression; Gibberellins; Microsomes; Phenanthrenes; Phylogeny; Picea; Pinus; Plant Proteins; Resins, Plant; Saccharomyces cerevisiae; Transcriptome

2016
Isopimaric acid from Pinus nigra shows activity against multidrug-resistant and EMRSA strains of Staphylococcus aureus.
    Phytotherapy research : PTR, 2005, Volume: 19, Issue:6

    The diterpene isopimaric acid was extracted from the immature cones of Pinus nigra (Arnold) using bioassay-guided fractionation of a crude hexane extract. Isopimaric acid was assayed against multidrug-resistant (MDR) and methicillin-resistant Staphylococcus aureus (MRSA). The minimum inhibitory concentrations (MIC) were 32-64 microg/mL and compared with a commercially obtained resin acid, abietic acid, with MICs of 64 microg/mL. Resin acids are known to have antibacterial activity and are valued in traditional medicine for their antiseptic properties. These results show that isopimaric acid is active against MDR and MRSA strains of S. aureus which are becoming increasingly resistant to antibiotics. Both compounds were evaluated for modulation activity in combination with antibiotics, but did not potentiate the activity of the antibiotics tested. However, the compounds were also assayed in combination with the efflux pump inhibitor reserpine, to see if inhibition of the TetK or NorA efflux pump increased their activity. Interestingly, rather than a potentiation of activity by a reduction in MIC, a two to four-fold increase in MIC was seen. It may be that isopimaric acid and abietic acid are not substrates for these efflux pumps, but it is also possible that an antagonistic interaction with reserpine may render the antibiotics inactive. 1H-NMR of abietic acid and reserpine taken individually and in combination, revealed a shift in resonance of some peaks for both compounds when mixed together compared with the spectra of the compounds on their own. It is proposed that this may be due to complex formation between abietic acid and reserpine and that this complex formation is responsible for a reduction in activity and elevation of MIC.

    Topics: Abietanes; Anti-Bacterial Agents; Carboxylic Acids; Humans; Methicillin Resistance; Microbial Sensitivity Tests; Phenanthrenes; Phytotherapy; Pinus; Plant Extracts; Staphylococcus aureus; Stereoisomerism

2005
Selected resin acids in effluent and receiving waters derived from a bleached and unbleached kraft pulp and paper mill.
    Environmental toxicology and chemistry, 2003, Volume: 22, Issue:1

    Water samples were collected on three dates at 24 sites influenced by effluent from Georgia-Pacific's Palatka Pulp and Paper Mill Operation, a bleached and unbleached kraft mill near Palatka, Florida, USA. The sampling sites were located within the mill retention ponds, Rice Creek, and the St. John's River. Samples were analyzed by gas chromatography-mass spectrometry for abietic, dehydroabietic, and isopimaric acids, all of which are potentially toxic by-products of pulp production. Isopimaric acid concentrations greater than 12 mg/L were measured at the mill's effluent outfall but were less than 20 microg/L at the end of Rice Creek. This result indicates that the waters of Rice Creek provide dilution or conditions conducive for degradation or sorption of these compounds. Large differences in resin acid concentrations were observed between sampling events. In two sampling events, the maximum observed concentrations were less than 2 mg/L for each analyte. In a third sampling event, all of the compounds were detected at concentrations greater than 10 mg/L. Data from the three sample dates showed that resin acid concentrations were below 20 microg/L before the confluence of Rice Creek and the St. John's River in all cases.

    Topics: Abietanes; Carboxylic Acids; Diterpenes; Environmental Monitoring; Florida; Gas Chromatography-Mass Spectrometry; Industrial Waste; Paper; Phenanthrenes; Water Pollutants, Chemical; Water Supply

2003
Reactivity of Trametes laccases with fatty and resin acids.
    Applied microbiology and biotechnology, 2001, Volume: 55, Issue:3

    Lipophilic extractives commonly referred to as wood pitch or wood resin can have a negative impact on paper machine runnability and product quality. The lipophilic extractives are composed mainly of fatty acids, resin acids, sterols, steryl esters and triglycerides. In this work, the suitability of laccases for the modification of fatty and resin acids was studied, using two model fractions. In the treatments, resin and fatty acid dispersions were treated with two different laccases, i.e. laccases from Trametes hirsuta and T. villosa. Different chromatographic methods were used to elucidate the effects of laccase treatments on the chemistry of the fatty and resin acids. Both laccases were able to modify the fatty and resin acids to some extent. In the case of fatty acids, a decrease in the amount of linoleic, oleic and pinolenic acids was observed, whereas the modification of resin acids resulted in a reduced amount of conjugated resin acids.

    Topics: Abietanes; alpha-Linolenic Acid; Carboxylic Acids; Chromatography, Gas; Chromatography, Gel; Diterpenes; Fatty Acids; Laccase; Oleic Acid; Oxidoreductases; Phenanthrenes; Polyporaceae

2001
Enzyme cytochemical responses of mussels (Mytilus edulis) to resin acid constituents of pulp mill effluents.
    Bulletin of environmental contamination and toxicology, 1999, Volume: 63, Issue:4

    Topics: Abietanes; Animals; Bivalvia; Carboxylic Acids; Digestive System; Diterpenes; Epithelial Cells; Industry; NADPH Dehydrogenase; Paper; Phenanthrenes; Resins, Plant; Water Pollutants, Chemical

1999