Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1978 May;61(5):737–742. doi: 10.1104/pp.61.5.737

Metabolism of Monoterpenes

Acetylation of (—)-Menthol by a Soluble Enzyme Preparation from Peppermint (Mentha piperita) Leaves 1

Rodney Croteau 1, Caroline Lee Hooper 1
PMCID: PMC1091967  PMID: 16660375

Abstract

The essential oil from mature leaves of flowering peppermint (Mentha piperita L.) contains up to 15% (—)-menthyl acetate, and leaf discs converted exogenous (—)-[G-3H]menthol into this ester in approximately 15% yield of the incorporated precursor. Leaf extracts catalyzed the acetyl coenzyme A-dependent acetylation of (—)-[G-3H]menthol and the product of this transacetylase reaction was identified by radiochromatographic techniques. Transacetylase activity was located mainly in the 100,000g supernatant fraction, and the preparation was partially purified by combination of Sephadex G-100 gel filtration and chromatography on O-diethylaminoethyl-cellulose. The transacetylase had a molecular weight of about 37,000 as judged by Sephadex G-150 gel filtration, and a pH optimum near 9. The apparent Km and velocity for (—)-menthol were 0.3 mm and 16 nmol/hr· mg of protein, respectively. The saturation curve for acetyl coenzyme A was sigmoidal, showing apparent saturation near 0.1 mm. Dithioerythritol was required for maximum activity and stability of the enzyme, and the enzyme was inhibited by thiol directed reagents such as p-hydroxymercuribenzoate. Diisopropylfluorophosphate also inhibited transacylation suggesting the involvement of a serine residue in catalysis. The transacylase was highly specific for acetyl coenzyme A; propionyl coenzyme A and butyryl coenzyme A were not nearly as efficient as acyl donors (11% and 2%, respectively). However, the enzyme was much less selective with regard to the alcohol substrate, suggesting that the nature of the acetate ester synthesized in mint is more dependent on the type of alcohol available than on the specificity of the transacetylase. This is the first report on an enzyme involved in monoterpenol acetylation in plants. A very similar enzyme, catalyzing this key reaction in the metabolism of menthol, was also isolated from the flowers of peppermint.

Full text

PDF
737

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BATTAILE J., LOOMIS W. D. Biosynthesis of terpenes. II. The site and sequence of terpene formation in peppermint. Biochim Biophys Acta. 1961 Aug 19;51:545–552. doi: 10.1016/0006-3002(61)90612-6. [DOI] [PubMed] [Google Scholar]
  2. Bonner W. M., Bloch K. Purification and properties of fatty acyl thioesterase I from Escherichia coli. J Biol Chem. 1972 May 25;247(10):3123–3133. [PubMed] [Google Scholar]
  3. Burbott A. J., Loomis W. D. Effects of light and temperature on the monoterpenes of peppermint. Plant Physiol. 1967 Jan;42(1):20–28. doi: 10.1104/pp.42.1.20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Burbott A. J., Loomis W. D. Evidence for metabolic turnover of monoterpenes in peppermint. Plant Physiol. 1969 Feb;44(2):173–179. doi: 10.1104/pp.44.2.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Croteau R., Karp F. Biosynthesis of monoterpenes: enzymatic concersion of neryl pyrophosphate to 1,8-cineole, alpha-terpineol, and cyclic monoterpene hydrocarbons by a cell-free preparation from sage (Salvia officinalis). Arch Biochem Biophys. 1976 Oct;176(2):734–746. doi: 10.1016/0003-9861(76)90217-4. [DOI] [PubMed] [Google Scholar]
  6. Croteau R., Kolattukudy P. E. Biosynthesis of hydroxyfatty acid polymers. Enzymatic synthesis of cutin from monomer acids by cell-free preparations from the epidermis of Vicia faba leaves. Biochemistry. 1974 Jul 16;13(15):3193–3202. doi: 10.1021/bi00712a030. [DOI] [PubMed] [Google Scholar]
  7. Friedhoff A. J., Miller J. C. In vitro and in vivo studies of extrapineal N-acetyltransferase of rat brain. Res Commun Chem Pathol Pharmacol. 1977 Feb;16(2):225–244. [PubMed] [Google Scholar]
  8. GOODMAN D. S., DEYKIN D., SHIRATORI T. THE FORMATION OF CHOLESTEROL ESTERS WITH RAT LIVER ENZYMES. J Biol Chem. 1964 May;239:1335–1345. [PubMed] [Google Scholar]
  9. Kolattukudy P. E. Mechanisms of synthesis of waxy esters in broccoli (Brassica oleracea). Biochemistry. 1967 Sep;6(9):2705–2717. doi: 10.1021/bi00861a010. [DOI] [PubMed] [Google Scholar]
  10. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  11. Loomis W. D. Overcoming problems of phenolics and quinones in the isolation of plant enzymes and organelles. Methods Enzymol. 1974;31:528–544. doi: 10.1016/0076-6879(74)31057-9. [DOI] [PubMed] [Google Scholar]
  12. Potty V. H. Determination of proteins in the presence of phenols and pectins. Anal Biochem. 1969 Jun;29(3):535–539. doi: 10.1016/0003-2697(69)90339-x. [DOI] [PubMed] [Google Scholar]
  13. REITSEMA R. H., CRAMER F. J., SCULLY N. J., CHORNEY W. Essential oil synthesis in mint. J Pharm Sci. 1961 Jan;50:18–21. doi: 10.1002/jps.2600500104. [DOI] [PubMed] [Google Scholar]
  14. Robinson J. B., Jr, Mahan D. E., Koeppe R. E. Studies on rat brain acyl-coenzyme A hydrolase (short chain). Biochem Biophys Res Commun. 1976 Aug 23;71(4):959–965. doi: 10.1016/0006-291x(76)90748-8. [DOI] [PubMed] [Google Scholar]
  15. Sharma S. K., Krishna Murti C. R. Production of lipid peroxides by brain. J Neurochem. 1968 Feb;15(2):147–149. doi: 10.1111/j.1471-4159.1968.tb06187.x. [DOI] [PubMed] [Google Scholar]
  16. Skopp K., Hörster H. An Zucker gebundene reguläre Monoterpene, teil I Thymol-und carvacrolglykoside in thymus vulgaris. Planta Med. 1976 May;29(3):208–215. doi: 10.1055/s-0028-1097653. [DOI] [PubMed] [Google Scholar]
  17. Taskinen J., Nykänen L. Chemical composition of angelica root oil. Acta Chem Scand B. 1975;29(7):757–764. doi: 10.3891/acta.chem.scand.29b-0757. [DOI] [PubMed] [Google Scholar]
  18. Williams J. W., Northrop D. B. Purification and properties of gentamicin acetyltransferase I. Biochemistry. 1976 Jan 13;15(1):125–131. doi: 10.1021/bi00646a019. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES