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Effect of Light Availability on the Interaction between Maritime Pine and the Pine Weevil: Light Drives Insect Feeding Behavior But Also the Defensive Capabilities of the Host.

Frontiers in plant science

Suárez-Vidal E, López-Goldar X, Sampedro L, Zas R.
PMID: 28912787
Front Plant Sci. 2017 Aug 29;8:1452. doi: 10.3389/fpls.2017.01452. eCollection 2017.

Light is a major environmental factor that may determine the interaction between plants and herbivores in several ways, including top-down effects through changes in herbivore behavior and bottom-up effects mediated by alterations of plant physiology. Here we explored the...

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Suárez-Vidal E, López-Goldar X, Sampedro L, et al. Effect of Light Availability on the Interaction between Maritime Pine and the Pine Weevil: Light Drives Insect Feeding Behavior But Also the Defensive Capabilities of the Host. Front Plant Sci. 2017;8:1452doi: 10.3389/fpls.2017.01452.
Suárez-Vidal, E., López-Goldar, X., Sampedro, L., & Zas, R. (2017). Effect of Light Availability on the Interaction between Maritime Pine and the Pine Weevil: Light Drives Insect Feeding Behavior But Also the Defensive Capabilities of the Host. Frontiers in plant science, 81452. https://doi.org/10.3389/fpls.2017.01452
Suárez-Vidal, Estefanía, et al. "Effect of Light Availability on the Interaction between Maritime Pine and the Pine Weevil: Light Drives Insect Feeding Behavior But Also the Defensive Capabilities of the Host." Frontiers in plant science vol. 8 (2017): 1452. doi: https://doi.org/10.3389/fpls.2017.01452
Suárez-Vidal E, López-Goldar X, Sampedro L, Zas R. Effect of Light Availability on the Interaction between Maritime Pine and the Pine Weevil: Light Drives Insect Feeding Behavior But Also the Defensive Capabilities of the Host. Front Plant Sci. 2017 Aug 29;8:1452. doi: 10.3389/fpls.2017.01452. eCollection 2017. PMID: 28912787; PMCID: PMC5583597.
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New Labdane diterpenes from Hedychium yunnanense with cytotoxicity and inhibitory effects on nitric oxide production.

Natural product research

Li YP, Zhao SM, Xu JJ, Zeng GZ, Li Y, Tan NH, Yang Y.
PMID: 26965832
Nat Prod Res. 2016 Dec;30(23):2669-2674. doi: 10.1080/14786419.2016.1143829. Epub 2016 Mar 11.

Two new labdane diterpenes, hedychenoids A (1) and B (2), were isolated from the rhizomes of Hedychium yunnanense, together with four known ones hedychenone (3), forrestin A (4), villosin (5) and calcaratarin C (6). Their structures were determined on...

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Li YP, Zhao SM, Xu JJ, et al. New Labdane diterpenes from Hedychium yunnanense with cytotoxicity and inhibitory effects on nitric oxide production. Nat Prod Res. 2016;30(23):2669-2674doi: 10.1080/14786419.2016.1143829.
Li, Y. P., Zhao, S. M., Xu, J. J., Zeng, G. Z., Li, Y., Tan, N. H., & Yang, Y. (2016). New Labdane diterpenes from Hedychium yunnanense with cytotoxicity and inhibitory effects on nitric oxide production. Natural product research, 30(23), 2669-2674. https://doi.org/10.1080/14786419.2016.1143829
Li, Yu-Peng, et al. "New Labdane diterpenes from Hedychium yunnanense with cytotoxicity and inhibitory effects on nitric oxide production." Natural product research vol. 30,23 (2016): 2669-2674. doi: https://doi.org/10.1080/14786419.2016.1143829
Li YP, Zhao SM, Xu JJ, Zeng GZ, Li Y, Tan NH, Yang Y. New Labdane diterpenes from Hedychium yunnanense with cytotoxicity and inhibitory effects on nitric oxide production. Nat Prod Res. 2016 Dec;30(23):2669-2674. doi: 10.1080/14786419.2016.1143829. Epub 2016 Mar 11. PMID: 26965832.
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NaCl stress-induced changes in the essential oil quality and abietane diterpene yield and composition in common sage.

Journal of intercultural ethnopharmacology

Tounekti T, Khemira H.
PMID: 26401409
J Intercult Ethnopharmacol. 2015 Jul-Sep;4(3):208-16. doi: 10.5455/jice.20150405064135. Epub 2015 Apr 10.

AIM: The purpose of this study was to evaluate how increasing NaCl salinity in the medium can affects the essential oils (EOs) composition and phenolic diterpene content and yield in leaves of Salvia officinalis L. The protective role of...

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Tounekti T, Khemira H. NaCl stress-induced changes in the essential oil quality and abietane diterpene yield and composition in common sage. J Intercult Ethnopharmacol. 2015;4(3):208-16doi: 10.5455/jice.20150405064135.
Tounekti, T., & Khemira, H. (2015). NaCl stress-induced changes in the essential oil quality and abietane diterpene yield and composition in common sage. Journal of intercultural ethnopharmacology, 4(3), 208-16. https://doi.org/10.5455/jice.20150405064135
Tounekti, Taieb, and Khemira, Habib. "NaCl stress-induced changes in the essential oil quality and abietane diterpene yield and composition in common sage." Journal of intercultural ethnopharmacology vol. 4,3 (2015): 208-16. doi: https://doi.org/10.5455/jice.20150405064135
Tounekti T, Khemira H. NaCl stress-induced changes in the essential oil quality and abietane diterpene yield and composition in common sage. J Intercult Ethnopharmacol. 2015 Jul-Sep;4(3):208-16. doi: 10.5455/jice.20150405064135. Epub 2015 Apr 10. PMID: 26401409; PMCID: PMC4579490.
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Effects of diterpene esters of tigliane, daphnane, ingenane, and lathyrane types on pink bollworm,Pectinophora gossypiella saunders (Lepidoptera: Gelechiidae).

Journal of chemical ecology

Marshall GT, Klocke JA, Lin LJ, Douglas Kinghorn A.
PMID: 24309846
J Chem Ecol. 1985 Feb;11(2):191-206. doi: 10.1007/BF00988202.

Twenty esters, representing the biogenetically related tigliane, daphnane, ingenane, and lathyrane series of diterpenes, were screened for growth-inhibitory and insecticidal effects on newly hatched larvae of the North American cotton pest,Pectinophora gossypiella (pink bollworm). Among the tigliane derivatives tested,...

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Marshall GT, Klocke JA, Lin LJ, et al. Effects of diterpene esters of tigliane, daphnane, ingenane, and lathyrane types on pink bollworm,Pectinophora gossypiella saunders (Lepidoptera: Gelechiidae). J Chem Ecol. 1985;11(2):191-206doi: 10.1007/BF00988202.
Marshall, G. T., Klocke, J. A., Lin, L. J., & Douglas Kinghorn, A. (1985). Effects of diterpene esters of tigliane, daphnane, ingenane, and lathyrane types on pink bollworm,Pectinophora gossypiella saunders (Lepidoptera: Gelechiidae). Journal of chemical ecology, 11(2), 191-206. https://doi.org/10.1007/BF00988202
Marshall, G T, et al. "Effects of diterpene esters of tigliane, daphnane, ingenane, and lathyrane types on pink bollworm,Pectinophora gossypiella saunders (Lepidoptera: Gelechiidae)." Journal of chemical ecology vol. 11,2 (1985): 191-206. doi: https://doi.org/10.1007/BF00988202
Marshall GT, Klocke JA, Lin LJ, Douglas Kinghorn A. Effects of diterpene esters of tigliane, daphnane, ingenane, and lathyrane types on pink bollworm,Pectinophora gossypiella saunders (Lepidoptera: Gelechiidae). J Chem Ecol. 1985 Feb;11(2):191-206. doi: 10.1007/BF00988202. PMID: 24309846.
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Heterologous expression of the isopimaric acid pathway in Nicotiana benthamiana and the effect of N-terminal modifications of the involved cytochrome P450 enzyme.

Journal of biological engineering

Gnanasekaran T, Vavitsas K, Andersen-Ranberg J, Nielsen AZ, Olsen CE, Hamberger B, Jensen PE.
PMID: 26702299
J Biol Eng. 2015 Dec 22;9:24. doi: 10.1186/s13036-015-0022-z. eCollection 2015.

BACKGROUND: Plant terpenoids are known for their diversity, stereochemical complexity, and their commercial interest as pharmaceuticals, food additives, and cosmetics. Developing biotechnology approaches for the production of these compounds in heterologous hosts can increase their market availability, reduce their...

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Gnanasekaran T, Vavitsas K, Andersen-Ranberg J, et al. Heterologous expression of the isopimaric acid pathway in Nicotiana benthamiana and the effect of N-terminal modifications of the involved cytochrome P450 enzyme. J Biol Eng. 2015;9:24doi: 10.1186/s13036-015-0022-z.
Gnanasekaran, T., Vavitsas, K., Andersen-Ranberg, J., Nielsen, A. Z., Olsen, C. E., Hamberger, B., & Jensen, P. E. (2015). Heterologous expression of the isopimaric acid pathway in Nicotiana benthamiana and the effect of N-terminal modifications of the involved cytochrome P450 enzyme. Journal of biological engineering, 924. https://doi.org/10.1186/s13036-015-0022-z
Gnanasekaran, Thiyagarajan, et al. "Heterologous expression of the isopimaric acid pathway in Nicotiana benthamiana and the effect of N-terminal modifications of the involved cytochrome P450 enzyme." Journal of biological engineering vol. 9 (2015): 24. doi: https://doi.org/10.1186/s13036-015-0022-z
Gnanasekaran T, Vavitsas K, Andersen-Ranberg J, Nielsen AZ, Olsen CE, Hamberger B, Jensen PE. Heterologous expression of the isopimaric acid pathway in Nicotiana benthamiana and the effect of N-terminal modifications of the involved cytochrome P450 enzyme. J Biol Eng. 2015 Dec 22;9:24. doi: 10.1186/s13036-015-0022-z. eCollection 2015. PMID: 26702299; PMCID: PMC4688937.
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Biological activities of Croton palanostigma Klotzsch.

Pharmacognosy magazine

Mota EF, Rosario DM, Silva Veiga AS, Barros Brasil Ddo S, Silveira FT, Dolabela MF.
PMID: 27041867
Pharmacogn Mag. 2016 Jan;12:S96-S101. doi: 10.4103/0973-1296.176109. Epub 2016 Feb 10.

BACKGROUND: Different species of Croton are used in traditional Amazonian medicine. Among the popular uses are treatment of bacterial diseases, poorly healing wounds and fevers.OBJECTIVE: This study evaluated the antileishmanial, antiplasmodial and antimicrobial activities of the extracts and diterpenes...

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Mota EF, Rosario DM, Silva Veiga AS, et al. Biological activities of Croton palanostigma Klotzsch. Pharmacogn Mag. 2016;12:S96-S101doi: 10.4103/0973-1296.176109.
Mota, E. F., Rosario, D. M., Silva Veiga, A. S., Barros Brasil, D. d. o. . S., Silveira, F. T., & Dolabela, M. F. (2016). Biological activities of Croton palanostigma Klotzsch. Pharmacognosy magazine, 12S96-S101. https://doi.org/10.4103/0973-1296.176109
Mota, Eduardo Ferreira, et al. "Biological activities of Croton palanostigma Klotzsch." Pharmacognosy magazine vol. 12 (2016): S96-S101. doi: https://doi.org/10.4103/0973-1296.176109
Mota EF, Rosario DM, Silva Veiga AS, Barros Brasil Ddo S, Silveira FT, Dolabela MF. Biological activities of Croton palanostigma Klotzsch. Pharmacogn Mag. 2016 Jan;12:S96-S101. doi: 10.4103/0973-1296.176109. Epub 2016 Feb 10. PMID: 27041867; PMCID: PMC4792008.
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Chemical ecology of canarian laurel forest: Toxic diterpenes fromPersea indica (Lauraceae).

Journal of chemical ecology

Gonzalez-Coloma A, Hernandez MG, Perales A, Fraga BM.
PMID: 24264325
J Chem Ecol. 1990 Sep;16(9):2723-33. doi: 10.1007/BF00988081.

The tree speciesP. indica (Lauraceae) is an important endemism in the Canary Islands laurel forest and can readily be distinguished by its defoliated appearance due to the seasonal action of wild rats (Rattus rattus), which eat the plant and...

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Gonzalez-Coloma A, Hernandez MG, Perales A, et al. Chemical ecology of canarian laurel forest: Toxic diterpenes fromPersea indica (Lauraceae). J Chem Ecol. 1990;16(9):2723-33doi: 10.1007/BF00988081.
Gonzalez-Coloma, A., Hernandez, M. G., Perales, A., & Fraga, B. M. (1990). Chemical ecology of canarian laurel forest: Toxic diterpenes fromPersea indica (Lauraceae). Journal of chemical ecology, 16(9), 2723-33. https://doi.org/10.1007/BF00988081
Gonzalez-Coloma, A, et al. "Chemical ecology of canarian laurel forest: Toxic diterpenes fromPersea indica (Lauraceae)." Journal of chemical ecology vol. 16,9 (1990): 2723-33. doi: https://doi.org/10.1007/BF00988081
Gonzalez-Coloma A, Hernandez MG, Perales A, Fraga BM. Chemical ecology of canarian laurel forest: Toxic diterpenes fromPersea indica (Lauraceae). J Chem Ecol. 1990 Sep;16(9):2723-33. doi: 10.1007/BF00988081. PMID: 24264325.
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Acetylated DNA-damaging clerodane diterpenes from Casearia sylvestris.

Phytochemistry

de Carvalho PR, Furlan M, Young MC, Kingston DG, Bolzani VS.
PMID: 11711078
Phytochemistry. 1998 Nov 20;49(6):1659-1662. doi: 10.1016/s0031-9422(98)00249-0.

In addition to the known diterpene casearin G (1), two new clerodane diterpene casearins type, casearin S (2) and casearin T (3), were isolated from an acetylated bioactive CH(2)Cl(2)/MeOH extract from leaves of Casearia sylvestris. The diterpenes 1-3 exhibited...

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de Carvalho PR, Furlan M, Young MC, et al. Acetylated DNA-damaging clerodane diterpenes from Casearia sylvestris. Phytochemistry. 1998;49(6):1659-1662doi: 10.1016/s0031-9422(98)00249-0.
de Carvalho, P. R., Furlan, M., Young, M. C., Kingston, D. G., & Bolzani, V. S. (1998). Acetylated DNA-damaging clerodane diterpenes from Casearia sylvestris. Phytochemistry, 49(6), 1659-1662. https://doi.org/10.1016/s0031-9422(98)00249-0
de Carvalho, Paulo Roberto F., et al. "Acetylated DNA-damaging clerodane diterpenes from Casearia sylvestris." Phytochemistry vol. 49,6 (1998): 1659-1662. doi: https://doi.org/10.1016/s0031-9422(98)00249-0
de Carvalho PR, Furlan M, Young MC, Kingston DG, Bolzani VS. Acetylated DNA-damaging clerodane diterpenes from Casearia sylvestris. Phytochemistry. 1998 Nov 20;49(6):1659-1662. doi: 10.1016/s0031-9422(98)00249-0. PMID: 11711078.
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New furanocembranoid diterpenes from the soft coral sinularia maxima .

Journal of natural products

Venkateswarlu Y, Sridevi KV, Rao MR.
PMID: 10346962
J Nat Prod. 1999 May;62(5):756-8. doi: 10.1021/np9804076.

The soft coral Sinularia maxima yielded five terpenoids and one sterol, including two new furanocembranoid diterpenoids (1 and 2). The structures of these new compounds were determined by the interpretation of their spectral data.

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Venkateswarlu Y, Sridevi KV, Rao MR. New furanocembranoid diterpenes from the soft coral sinularia maxima . J Nat Prod. 1999;62(5):756-8doi: 10.1021/np9804076.
Venkateswarlu, Y., Sridevi, K. V., & Rao, M. R. (1999). New furanocembranoid diterpenes from the soft coral sinularia maxima . Journal of natural products, 62(5), 756-8. https://doi.org/10.1021/np9804076
Venkateswarlu, et al. "New furanocembranoid diterpenes from the soft coral sinularia maxima ." Journal of natural products vol. 62,5 (1999): 756-8. doi: https://doi.org/10.1021/np9804076
Venkateswarlu Y, Sridevi KV, Rao MR. New furanocembranoid diterpenes from the soft coral sinularia maxima . J Nat Prod. 1999 May;62(5):756-8. doi: 10.1021/np9804076. PMID: 10346962.
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The steam volatile oil of Wollemia nobilis and its comparison with other members of the Araucariaceae (Agathis and Araucaria).

Biochemical systematics and ecology

Brophy JJ, Goldsack RJ, Wu MZ, Fookes CJ, Forster PI.
PMID: 10793256
Biochem Syst Ecol. 2000 Jul 01;28(6):563-578. doi: 10.1016/s0305-1978(99)00090-3.

The leaf essential oil of Wollemia nobilis (Wollemi Pine) has been investigated and compared with other members of the family Araucariaceae. All araucaroids examined yielded steam volatile oils in low yields. The oil from Wollemia nobilis was composed mainly...

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Brophy JJ, Goldsack RJ, Wu MZ, et al. The steam volatile oil of Wollemia nobilis and its comparison with other members of the Araucariaceae (Agathis and Araucaria). Biochem Syst Ecol. 2000;28(6):563-578doi: 10.1016/s0305-1978(99)00090-3.
Brophy, J. J., Goldsack, R. J., Wu, M. Z., Fookes, C. J., & Forster, P. I. (2000). The steam volatile oil of Wollemia nobilis and its comparison with other members of the Araucariaceae (Agathis and Araucaria). Biochemical systematics and ecology, 28(6), 563-578. https://doi.org/10.1016/s0305-1978(99)00090-3
Brophy, et al. "The steam volatile oil of Wollemia nobilis and its comparison with other members of the Araucariaceae (Agathis and Araucaria)." Biochemical systematics and ecology vol. 28,6 (2000): 563-578. doi: https://doi.org/10.1016/s0305-1978(99)00090-3
Brophy JJ, Goldsack RJ, Wu MZ, Fookes CJ, Forster PI. The steam volatile oil of Wollemia nobilis and its comparison with other members of the Araucariaceae (Agathis and Araucaria). Biochem Syst Ecol. 2000 Jul 01;28(6):563-578. doi: 10.1016/s0305-1978(99)00090-3. PMID: 10793256.
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Synthetic Studies on the Ingenane Diterpenes. Direct Conversion of the out,out-Bicyclo[4.4.1]undecane System into a Highly Strained In,out Stereoisomer.

The Journal of organic chemistry

Rigby JH, de Sainte Claire V, Cuisiat SV, Heeg MJ.
PMID: 11667774
J Org Chem. 1996 Nov 15;61(23):7992-7993. doi: 10.1021/jo961714o.

No abstract available.

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Rigby JH, de Sainte Claire V, Cuisiat SV, et al. Synthetic Studies on the Ingenane Diterpenes. Direct Conversion of the out,out-Bicyclo[4.4.1]undecane System into a Highly Strained In,out Stereoisomer. J Org Chem. 1996;61(23):7992-7993doi: 10.1021/jo961714o.
Rigby, J. H., de Sainte Claire, V., Cuisiat, S. V., & Heeg, M. J. (1996). Synthetic Studies on the Ingenane Diterpenes. Direct Conversion of the out,out-Bicyclo[4.4.1]undecane System into a Highly Strained In,out Stereoisomer. The Journal of organic chemistry, 61(23), 7992-7993. https://doi.org/10.1021/jo961714o
Rigby, James H., et al. "Synthetic Studies on the Ingenane Diterpenes. Direct Conversion of the out,out-Bicyclo[4.4.1]undecane System into a Highly Strained In,out Stereoisomer." The Journal of organic chemistry vol. 61,23 (1996): 7992-7993. doi: https://doi.org/10.1021/jo961714o
Rigby JH, de Sainte Claire V, Cuisiat SV, Heeg MJ. Synthetic Studies on the Ingenane Diterpenes. Direct Conversion of the out,out-Bicyclo[4.4.1]undecane System into a Highly Strained In,out Stereoisomer. J Org Chem. 1996 Nov 15;61(23):7992-7993. doi: 10.1021/jo961714o. PMID: 11667774.
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Chlorsulfuron modifies biosynthesis of acyl Acid substituents of sucrose esters secreted by tobacco trichomes.

Plant physiology

Kandra L, Wagner GJ.
PMID: 16667871
Plant Physiol. 1990 Nov;94(3):906-12. doi: 10.1104/pp.94.3.906.

Sucrose esters and duvatrienediol diterpenes are principal constituents formed in and secreted outside head cells of trichomes occurring on surfaces of Nicotiana tabacum. Using trichome-bearing epidermal peels prepared from midveins of N. tabacum cv T.I. 1068 leaves, we found...

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Kandra L, Wagner GJ. Chlorsulfuron modifies biosynthesis of acyl Acid substituents of sucrose esters secreted by tobacco trichomes. Plant Physiol. 1990;94(3):906-12doi: 10.1104/pp.94.3.906.
Kandra, L., & Wagner, G. J. (1990). Chlorsulfuron modifies biosynthesis of acyl Acid substituents of sucrose esters secreted by tobacco trichomes. Plant physiology, 94(3), 906-12. https://doi.org/10.1104/pp.94.3.906
Kandra, L, and Wagner, G J. "Chlorsulfuron modifies biosynthesis of acyl Acid substituents of sucrose esters secreted by tobacco trichomes." Plant physiology vol. 94,3 (1990): 906-12. doi: https://doi.org/10.1104/pp.94.3.906
Kandra L, Wagner GJ. Chlorsulfuron modifies biosynthesis of acyl Acid substituents of sucrose esters secreted by tobacco trichomes. Plant Physiol. 1990 Nov;94(3):906-12. doi: 10.1104/pp.94.3.906. PMID: 16667871; PMCID: PMC1077321.
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Showing 1 to 12 of 358 entries