» Articles » PMID: 16664523

Direct Demonstration of Duvatrienediol Biosynthesis in Glandular Heads of Tobacco Trichomes

Overview
Journal Plant Physiol
Specialty Physiology
Date 1985 Dec 1
PMID 16664523
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Biosynthesis of the diterpenes, alpha and beta 4,8,13-duvatriene-1,3-diol, has been observed in detached, intact glandular heads from trichomes of Nicotiana tabacum, Tobacco Introduction 1068. This result shows directly that the glandular head portion of the trichome is capable of duvatrienediol biosynthesis. In additional experiments, all of the [(14)C] duvatrienediol formed from sodium [2-(14)C]acetate by leaf midrib sections was recovered with trichome exudate and surface washes. None was found in trichome stalk, epidermal or subepidermal tissue extracts. Also, removal of glandular heads and exudate from midrib sections reduced or eliminated duvatrienediol biosynthetic capacity. Together these results strongly suggest that glandular heads are the primary, and perhaps the only, site of duvatrienediol biosynthesis in this plant.Incubation of detached, intact glandular heads with sodium [(14)C]acetate in the dark or incubation in the light in the presence of DCMU reduced incorporation into duvatrienediols by 97%. These results suggest that chloroplasts which are abundant in glandular heads are involved in the biogenesis of these compounds.

Citing Articles

Characteristics of the phyllosphere microbial community and its relationship with major aroma precursors during the tobacco maturation process.

Shi Y, He Y, Zheng Y, Liu X, Wang S, Xiong T Front Plant Sci. 2024; 15:1346154.

PMID: 38799095 PMC: 11116568. DOI: 10.3389/fpls.2024.1346154.


Sclareol and linalyl acetate are produced by glandular trichomes through the MEP pathway.

Chalvin C, Drevensek S, Gilard F, Mauve C, Chollet C, Morin H Hortic Res. 2021; 8(1):206.

PMID: 34593779 PMC: 8484277. DOI: 10.1038/s41438-021-00640-w.


Glandular trichomes of the flowers and leaves in Millingtonia hortensis (Bignoniaceae).

Muravnik L, Mosina A, Zaporozhets N, Bhattacharya R, Saha S, Ghissing U Planta. 2021; 253(1):13.

PMID: 33389109 DOI: 10.1007/s00425-020-03541-9.


Plant Glandular Trichomes: Natural Cell Factories of High Biotechnological Interest.

Huchelmann A, Boutry M, Hachez C Plant Physiol. 2017; 175(1):6-22.

PMID: 28724619 PMC: 5580781. DOI: 10.1104/pp.17.00727.


Photosynthetic Trichomes Contain a Specific Rubisco with a Modified pH-Dependent Activity.

Laterre R, Pottier M, Remacle C, Boutry M Plant Physiol. 2017; 173(4):2110-2120.

PMID: 28250069 PMC: 5373067. DOI: 10.1104/pp.17.00062.


References
1.
Chang S, Grunwald C . Duvatrienediols in cuticular wax of Burley tobacco leaves. J Lipid Res. 1976; 17(1):7-11. View

2.
SLATER E . The mechanism of action of the respiratory inhibitor, antimycin. Biochim Biophys Acta. 1973; 301(2):129-54. DOI: 10.1016/0304-4173(73)90002-5. View

3.
Uriel J, Berges J . Characterization of natural inhibitors of trypsin and chymotrypsin by electrophoresis in acrylamide-agarose gels. Nature. 1968; 218(5141):578-80. DOI: 10.1038/218578b0. View

4.
VOORS A, Shuman M, Johnson W . Additive statistical effects of cadmium and lead on heart-related disease in a North Carolina autopsy series. Arch Environ Health. 1982; 37(2):98-102. DOI: 10.1080/00039896.1982.10667544. View