The useful biological properties of sucrose esters: Opportunities for the development of new functional foods

References

• Abubakar, A., A. Y. Bala, and K. Singh. 2017. Plant molluscicides and their modes of action: A review. International Journal of Advanced Scientific Research 2 (1):37–49.
   Google Scholar
• Assmann, G., P. Buono, A. Daniele, E. Della Valle, E. Farinaro, G. Ferns, V. Krogh, D. Kromhout, L. Masana, J. Merino, et al. 2014. Functional foods and cardiometabolic diseases: International task force for prevention of cardiometabolic diseases. Nutrition, Metabolism, and Cardiovascular Diseases: NMCD 24 (12):1272–300. doi: 10.1016/j.numecd.2014.10.010.
   PubMed Web of Science ®Google Scholar
• Bauchot, A. D., P. John, Y. Soria, and I. Recasens. 1995. Sucrose ester-based coatings formulated with food-compatible antioxidants in the prevention of superficial scald in stored apples. Journal of the American Society for Horticultural Science 120 (3):491–6. doi: 10.21273/JASHS.120.3.491.
   Google Scholar
• Buta, J. G., W. R. Lusby, J. W. Neal, Jr., R. M. Waters, and G. W. Pittarelli. 1993. Sucrose esters from Nicotiana gossei active against the greenhouse whitefly Trialeuroides vaporariorum. Phytochemistry 32 (4):859–64. doi: 10.1016/0031-9422(93)85220-L.
   Google Scholar
• Cao, H., O. Saroglu, A. Karadag, Z. Diaconeasa, G. Zoccatelli, C. A. Conte-Junior, G. A. Gonzalez-Aguilar, J. Ou, W. Bai, C. M. Zamarioli, et al. 2021. Available technologies on improving the stability of polyphenols in food processing. Food Frontiers 2 (2):109–39. doi: 10.1002/fft2.65.
   Google Scholar
• Chang, S. W., and J. F. Shaw. 2009. Biocatalysis for the production of carbohydrate esters. New Biotechnology 26 (3–4):109–16. doi: 10.1016/j.nbt.2009.07.003.
   PubMed Web of Science ®Google Scholar
• Chhillar, H., P. Chopra, and M. A. Ashfaq. 2021. Lignans from linseed (Linum usitatissimum L.) and its allied species: Retrospect, introspect and prospect. Critical Reviews in Food Science and Nutrition 61 (16):2719–41. doi: 10.1080/10408398.2020.1784840.
   PubMed Web of Science ®Google Scholar
• Chortyk, O. T. 1994. Chemically synthesized sugar esters for the control of soft-bodied arthropods. US Patent 6,608,039 B1, filed July 11, 1994, and issued August 19, 2003. https://patents.google.com/patent/US6608039B1.
   Google Scholar
• Chortyk, O. T., S. J. Kays, and Q. Teng. 1997. Characterization of insecticidal sugar esters of Petunia. Journal of Agricultural and Food Chemistry 45 (1):270–5. doi: 10.1021/jf960322f.
   Google Scholar
• Chortyk, O. T., J. G. Pomonis, and A. W. Johnson. 1996. Syntheses and characterizations of insecticidal sucrose esters. Journal of Agricultural and Food Chemistry 44 (6):1551–7. doi: 10.1021/jf950615t.
   Web of Science ®Google Scholar
• Chortyk, O. T., R. F. Severson, H. C. Cutler, and V. A. Sisson. 1993. Antibiotic activities of sugar esters isolated from selected Nicotiana species. Bioscience, Biotechnology, and Biochemistry 57 (8):1355–6. doi: 10.1271/bbb.57.1355.
   PubMed Web of Science ®Google Scholar
• Cutler, H. G., R. F. Severson, P. D. Cole, D. M. Jackson, and A. W. Johnson. 1986. Secondary metabolites from higher plants: Their possible role as biological control agents. In Natural resistance of plants to pests. ACS symposium series, ed. M. G. Green and P. A. Hedin, vol. 296, 178–96. Washington, DC: American Chemical Society. doi: 10.1021/bk-1986-0296.ch015.
   Google Scholar
• Deng, R., W. Li, M. A. Berhow, G. Jander, and S. Zhou. 2022. Phenolic sucrose esters: Evolution, regulation, biosynthesis, and biological functions. Plant Molecular Biology 109 (4–5):369–83. doi: 10.1007/s11103-021-01142-y.
   PubMedGoogle Scholar
• Devulapalle, K. S., A. Segura, M. Ferrer, M. Alcalde, G. Mooser, and F. J. Plou. 2004. Effect of carbohydrate fatty acid esters on Streptococcus sobrinus and glucosyltransferase activity. Carbohydrate Research 339 (6):1029–34. doi: 10.1016/j.carres.2004.01.007.
   PubMed Web of Science ®Google Scholar
• Egerton-Warburton, L. M., and E. L. Ghisalberti. 2001. Isolation and structural identification of a germination inhibitor in fire-recruiters from the California chaparral. Journal of Chemical Ecology 27 (2):371–82. doi: 10.1023/A:1005688623977.
   PubMedGoogle Scholar
• European Food Safety Authority (EFSA). 2004. Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) on Sucrose esters of fatty acids E 473 and sucroglycerides E 474. EFSA Journal 106:1–24. https://www.efsa.europa.eu/en/efsajournal/pub/106.
   Google Scholar
• Fabre, N., P. Urizzi, J. P. Souchard, A. Fréchard, C. Claparols, I. Fourasté, and C. Moulis. 2000. An antioxidant sinapic acid ester isolated from Iberis amara. Fitoterapia 71 (4):425–8.
   PubMed Web of Science ®Google Scholar
• Fan, P., A. M. Miller, A. L. Schilmiller, X. Liu, I. Ofner, A. D. Jones, D. Zamir, and R. L. Last. 2016. In vitro reconstruction and analysis of evolutionary variation of the tomato acylsucrose metabolic network. Proceedings of the National Academy of Sciences 113 (2):E239–E248. doi: 10.1073/pnas.1517930113.
   PubMedGoogle Scholar
• Fang, X., Z.-G. Zhuo, X.-K. Xu, J. Ye, H.-L. Li, Y.-H. Shen, and W.-D. Zhang. 2017. Cytotoxic isovaleryl sucrose esters from Ainsliaea yunnanensis: Reduction of mitochondrial membrane potential and increase of reactive oxygen species levels in A549 cells. RSC Advances 7 (34):20865–73. doi: 10.1039/C7RA01986F.
   Web of Science ®Google Scholar
• Farone, W. A., T. Palmer, and G. J. Puterka. 2000. Polyol ester insecticides and method of synthesis. US Patent 6 419,941 B1, filed February 18, 2000, and issued July 16, 2002. https://patents.google.com/patent/US6419941B1.
   Google Scholar
• Farone, W. A., T. Palmer, and G. J. Puterka. 2002. Polyol ester insecticides. US Patent 6,756,046 B2, filed April 24, 2002, and issued June 29, 2004. https://patents.google.com/patent/US6756046B2.
   Google Scholar
• Franssen, M. C., P. Steunenberg, E. L. Scott, H. Zuilhof, and J. P. Sanders. 2013. Immobilised enzymes in biorenewables production. Chemical Society Reviews 42 (15):6491–533. doi: 10.1039/c3cs00004d.
   PubMed Web of Science ®Google Scholar
• Garegg, P. J., S. Oscarson, and H. Ritzén. 1988. Partially esterified sucrose derivatives: Synthesis of 6-O-acetyl-2, 3, 4-tri-O-[(S)-3-methylpentanoyl] sucrose, a naturally occurring flavour precursor of tobacco. Carbohydrate Research 181:89–96. doi: 10.1016/0008-6215(88)84025-4.
   Google Scholar
• Goffreda, J. C., J. C. Steffens, and M. A. Mutschler. 1990. Association of epicuticular sugars with aphid resistance in hybrids with wild tomato. Journal of the American Society for Horticultural Science 115 (1):161–5. doi: 10.21273/JASHS.115.1.161.
   Google Scholar
• Granato, D., F. J. Barba, D. B. Kovačević, J. M. Lorenzo, A. G. Cruz, and P. Putnik. 2020. Functional foods: Product development, technological trends, efficacy testing, and safety. Annual Review of Food Science and Technology 11 (1):93–118. doi: 10.1146/annurev-food-032519-051708.
   PubMedGoogle Scholar
• Guo, P., P. Zhao, J. Liu, H. Ma, J. Bai, Y. Cao, Y. Liu, H. He, and C. Qi. 2013. Preparation of a novel organoselenium compound and its anticancer effects on cervical cancer cell line HeLa. Biological Trace Element Research 151 (2):301–6. doi: 10.1007/s12011-012-9563-x.
   PubMedGoogle Scholar
• Habulin, M., S. Šabeder, and Ž. Knez. 2008. Enzymatic synthesis of sugar fatty acid esters in organic solvent and in supercritical carbon dioxide and their antimicrobial activity. The Journal of Supercritical Fluids 45 (3):338–45. doi: 10.1016/j.supflu.2008.01.002.
   Web of Science ®Google Scholar
• Haliński, Ł. P., and P. Stepnowski. 2016. Cuticular hydrocarbons and sucrose esters as chemotaxonomic markers of wild and cultivated tomato species (Solanum section Lycopersicon). Phytochemistry 132:57–67. doi: 10.1016/j.phytochem.2016.09.011.
   PubMedGoogle Scholar
• Holley, J. D., R. R. King, and R. P. Singh. 1987. Glandular trichomes and the resistance of Solanum berthaultii (PI 473340) to infection from Phytophthora infestans. Canadian Journal of Plant Pathology 9 (4):291–4. doi: 10.1080/07060668709501859.
   Web of Science ®Google Scholar
• Hu, Y., H. B. Liao, G. Dai-Hong, P. Liu, Y. Y. Wang, and K. Rahman. 2010. Antidepressant-like effects of 3,6′-disinapoyl sucrose on hippocampal neuronal plasticity and neurotrophic signal pathway in chronically mild stressed rats. Neurochemistry International 56 (3):461–5. doi: 10.1016/j.neuint.2009.12.004.
   PubMed Web of Science ®Google Scholar
• Isman, M. B. 2006. Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world. Annual Review of Entomology 51 (1):45–66. doi: 10.1146/annurev.ento.51.110104.151146.
   PubMed Web of Science ®Google Scholar
• Johnson, A., and R. Severson. 1984. Leaf surface chemistry of tobacco budworm resistant tobacco. Journal of Agricultural Entomology 1 (2):23–32.
   Google Scholar
• Kandra, L., and G. J. Wagner. 1988. Studies of the site and mode of biosynthesis of tobacco trichome exudate components. Archives of Biochemistry and Biophysics 265 (2):425–32.
   PubMedGoogle Scholar
• Kashyap, S., S. Khagta, K. Guleria, and V. Arya. 2019. Plants as molluscicides: A recent update. International Journal of Botany Studies 4 (1):50–6.
   Google Scholar
• Kato, A., K. Ando, G. Tamura, and K. Arima. 1971. Effects of some fatty acid esters on the viability and transplantability of Ehrlich ascites tumor cells. Cancer Research 31 (5):501–4.
   PubMedGoogle Scholar
• Katsuragi, T. 1999. Interactions between surfactants and fats. In Physical properties of fats, oils, and emulsifiers, ed. N. Widlak, 211–9. Champaign, IL: AOCS Press.
   Google Scholar
• Kays, S. J., R. F. Severson, S. F. Nottingham, R. B. Chalfant, and O. Chortyk. 1994. Possible biopesticide from Petunia for the control of the sweetpotato whitefly (Bemisia tabaci) on vegetable crops. Proceedings of the Florida State Horticultural Society 107:163–7.
   Google Scholar
• Kennedy, B. S., M. T. Nielsen, R. F. Severson, V. A. Sisson, M. K. Stephenson, and D. M. Jackson. 1992. Leaf surface chemicals from Nicotiana affecting germination of Peronospora tabacina (Adam) sporangia. Journal of Chemical Ecology 18 (9):1467–79. doi: 10.1007/BF00993221.
   PubMed Web of Science ®Google Scholar
• Kim, K.-S., D.-S. Lee, G.-S. Bae, S.-J. Park, D.-G. Kang, H.-S. Lee, H. Oh, and Y.-C. Kim. 2013. The inhibition of JNK MAPK and NF-κB signaling by tenuifoliside A isolated from Polygala tenuifolia in lipopolysaccharide-induced macrophages is associated with its anti-inflammatory effect. European Journal of Pharmacology 721 (1–3):267–76.
   PubMed Web of Science ®Google Scholar
• King, R. R., L. A. Calhoun, R. P. Singh, and A. Boucher. 1993. Characterization of 2,3,4,3′-tetra-O-acylated sucrose esters associated with the glandular trichomes of Lycopersicon typicum. Journal of Agricultural and Food Chemistry 41 (3):469–73. doi: 10.1021/jf00027a023.
   Google Scholar
• King, R. R., Y. Pelletier, R. P. Singh, and L. A. Calhoun. 1986. 4-Di-O-Isobutyryl-6-O-caprylsucrose: The major component of a novel sucrose ester complex from the type B glandular trichomes of Solanum berthaultii Hawkes (Pl 473340). Journal of the Chemical Society, Chemical Communications 3 (14):1078–9.
   Google Scholar
• King, R. R., R. P. Singh, and L. A. Calhoun. 1987. Isolation and characterization of 3,3′,4,6-tetra-O-acylated sucrose esters from the type B glandular trichomes of Solanum berthaultii Hawkes (PI 265857). Carbohydrate Research 166 (1):113–21. doi: 10.1016/0008-6215(87)80048-4.
   Google Scholar
• King, R. R., R. P. Singh, and L. A. Calhoun. 1988. Elucidation of structures for a unique class of 2,3,4,3′-tetra-O-acylated sucrose esters from the type B glandular trichomes of Solanum neocardenasii Hawkes & Hjerting (PI 498129). Carbohydrate Research 173 (2):235–41. doi: 10.1016/S0008-6215(00)90819-X.
   Google Scholar
• Koul, O., R. Singh, A. Middha, S. Walia, P. Shukla, and D. Kanda. 2014. Toxicity of biorational glycol diesters and sucrose octanoate to selected horticultural insect pests. Biopesticides International 10 (2):126–35.
   Google Scholar
• Koul, O., G. Singh, R. Singh, A. Middha, S. Walia, P. Shukla, and V. K. Kaul. 2012. Biorational glycol diesters as dietary toxins versus bioefficacy of sucrose octanoate against lepidopteran larvae. Industrial Crops and Products 40:151–9. doi: 10.1016/j.indcrop.2012.03.010.
   Google Scholar
• Koul, O., G. Singh, R. Singh, S. Walia, and V. K. Kaul. 2009. Comparative bioefficacy of biorational ethylene glycol diesters and sucrose octanoate against Lipaphis erysimi (Homoptera: Aphididae). Journal of Applied Entomology 133 (9–10):682–8. doi: 10.1111/j.1439-0418.2009.01419.x.
   Google Scholar
• Kroumova, A. B., D. Zaitlin, and G. J. Wagner. 2016. Natural variability in acyl moieties of sugar esters produced by certain tobacco and other Solanaceae species. Phytochemistry 130:218–27. doi: 10.1016/j.phytochem.2016.05.008.
   PubMedGoogle Scholar
• Kumar, P. 2020. A review—on molluscs as an agricultural pest and their control. International Journal of Food Science and Agriculture 4 (4):383–9. doi: 10.26855/ijfsa.2020.12.004.
   Google Scholar
• Leckie, B. M., D. A. D’Ambrosio, T. M. Chappell, R. Halitschke, D. M. De Jong, A. Kessler, G. G. Kennedy, and M. A. Mutschler. 2016. Differential and synergistic functionality of acylsugars in suppressing oviposition by insect herbivores. PLoS One 11 (4):e0153345. doi: 10.1371/journal.pone.0153345.
   PubMedGoogle Scholar
• Li, S., Z. Song, Z. Liu, and S. Bai. 2008. Characterization and insecticidal activity of sucrose octanoates. Agronomy for Sustainable Development 28 (2):239–45. doi: 10.1051/agro:2007037.
   Google Scholar
• Li, X., X. Jiang, J. Sun, C. Zhu, X. Li, L. Tian, L. Liu, and W. Bai. 2017. Cytoprotective effects of dietary flavonoids against cadmium-induced toxicity. Annals of the New York Academy of Sciences 1398 (1):5–19. doi: 10.1111/nyas.13344.
   PubMed Web of Science ®Google Scholar
• Liu, P., Y. Hu, D. H. Guo, B. R. Lu, K. Rahman, L. H. Mu, and D. X. Wang. 2010. Antioxidant activity of oligosaccharide ester extracted from Polygala tenuifolia roots in senescence-accelerated mice. Pharmaceutical Biology 48 (7):828–33. doi: 10.3109/13880200903283707.
   PubMed Web of Science ®Google Scholar
• Liu, P., Y. Hu, D.-H. Guo, D.-X. Wang, H.-H. Tu, L. Ma, T.-T. Xie, and L.-Y. Kong. 2010. Potential antidepressant properties of Radix polygalae (Yuan Zhi). Phytomedicine 17 (10):794–9. doi: 10.1016/j.phymed.2010.01.004.
   PubMed Web of Science ®Google Scholar
• Liu, X., D. Wang, R. Zhao, X. Dong, Y. Hu, and P. Liu. 2016. Synergistic neuroprotective effects of two herbal ingredients via CREB-dependent pathway. Frontiers in Pharmacology 7 (337) doi: 10.3389/fphar.2016.00337.
   Google Scholar
• Lorenzo, J. M., P. E. S. Munekata, M. Pateiro, P. C. B. Campagnol, and R. Domínguez. 2016. Healthy Spanish salchichón enriched with encapsulated n-3 long chain fatty acids in konjac glucomannan matrix. Food Research International (Ottawa, Ont.) 89 (Pt 1):289–95. doi: 10.1016/j.foodres.2016.08.012.
   PubMedGoogle Scholar
• Maldonado, E., R. Torres, F. M. Martínez, and A. L. Pérez-Castorena. 2006. Sucrose esters from the fruits of Physalis nicandroides var. attenuata. Journal of Natural Products 69 (10):1511–3.
   PubMedGoogle Scholar
• Marshall, D. L., and L. B. Bullerman. 1986. Antimicrobial activity of sucrose fatty acid ester emulsifiers. Journal of Food Science 51 (2):468–70.
   Web of Science ®Google Scholar
• Martin, T. 2011. Insecticidal compositions suitable for use in preparation of insecticidal liquid fertilizers. US Patent 8,029,827 B2, filed September 9, 2011, and issued September 11, 2012. https://patents.google.com/patent/US8029827B2
   Google Scholar
• Matsuzaki, T., K. Koseki, and A. Koiwai. 1988. Germination and growth inhibition of surface lipids from Nicotiana species and identification of sucrose esters. Agricultural and Biological Chemistry 52 (8):1889–97.
   Web of Science ®Google Scholar
• Michaud, J. P., and C. L. McKenzie. 2004. Safety of a novel insecticide, sucrose octanoate, to beneficial insects in Florida citrus. Florida Entomologist 87 (1):6–9.
   Google Scholar
• Mitsubishi Chemical Corporation. 2022a. RYOTOTM SUGAR ESTER. Accessed September 30. https://www.m-chemical.co.jp/en/products/departments/mcc/food/product/1201443_9380.html.
   Google Scholar
• Mitsubishi Chemical Corporation. 2022b. Inhibition of thermal and freezing denaturation of proteins. Accessed September 20. https://www.mfc.co.jp/english/effect.htm.
   Google Scholar
• Miyase, T., H. Noguchi, and X. M. Chen. 1999. Sucrose esters and xanthone C-glycosides from the roots of Polygala sibirica. Journal of Natural Products 62 (7):993–6.
   PubMed Web of Science ®Google Scholar
• Momen, M. N., Y. Tatsumi, and K. Shimokawa. 1997. Effects of coating treatment with sucrose fatty acid esters on the ripening of Cavendish banana. Food Preservation Science 23 (6):315–22.
   Google Scholar
• Moser, D., I. Klaiber, B. Vogler, and W. Kraus. 1999. Molluscicidal and antibacterial compounds from Petunia hybrida. Pesticide Science 55 (3):336–9.
   Google Scholar
• Mousala, S. L., J. P. Villalta, I. F. Garcia, A. L. Cambil, and M. P. G. Pareja. 2007. Surface treatments and coatings for cheese and seeds (sunflower and pumpkin) with palmitic, lauric and estearic fatty acid esters with sucrose. EP Patent 1,980,162 A1, filed January 15, 2007, and issued October 15, 2008. https://patents.google.com/patent/EP1980162A1.
   Google Scholar
• Nakayama, M., D. Tomiyama, K. Ikeda, M. Katsuki, A. Nonaka, and T. Miyamoto. 2015. Antibacterial effects of monoglycerol fatty acid esters and sucrose fatty acid esters on Bacillus spp. Food Science and Technology Research 21 (3):431–7.
   Web of Science ®Google Scholar
• Nayak, S. L., S. Sethi, S. R. R. Harma, and U. Prajapati. 2019. Active edible coatings for fresh fruits and vegetables. In Polymers for agri-food applications, ed. T. J. Gutiérrez, 417–32. Cham, Switzerland: Springer. https://link.springer.com/chapter/10.1007/978-3-030-19416-1_21.
   Google Scholar
• Neal, J. J., W. M. Tingey, and J. C. Steffens. 1990. Sucrose esters of carboxylic acids in glandular trichomes of Solanum berthaultii deter settling and probing by green peach aphid. Journal of Chemical Ecology 16 (2):487–97.
   PubMedGoogle Scholar
• Neal, J. W., Jr., J. G. Buta, G. W. Pittarelli, W. R. Lusby, and J. A. Bentz. 1994. Novel sucrose esters from Nicotiana gossei: Effective biorationals against selected horticultural insect pests. Journal of Economic Entomology 87 (6):1600–7.
   Google Scholar
• Neta, N. S., J. A. Teixeira, and L. R. Rodrigues. 2015. Sugar ester surfactants: Enzymatic synthesis and applications in food industry. Critical Reviews in Food Science and Nutrition 55 (5):595–610.
   PubMed Web of Science ®Google Scholar
• Nishikawa, Y., M. Okabe, K. Yoshimoto, G. Kurono, and F. Fukuoka. 1976. Chemical and biochemical studies on carbohydrate esters. II. Antitumor activity of saturated fatty acids and their ester derivatives against Ehrlich ascites carcinoma. Chemical and Pharmaceutical Bulletin 24 (3):387–93.
   PubMed Web of Science ®Google Scholar
• Nishikawa, Y., K. Yoshimoto, T. Manabe, and T. Ikekawa. 1977. Chemical and biochemical studies on carbohydrate esters. VI. Further examinations on antitumor activities of stearoyl esters of sucrose. Chemical & Pharmaceutical Bulletin 25 (9):2378–84.
   PubMed Web of Science ®Google Scholar
• Nishikawa, Y., K. Yoshimoto, M. Okabe, and F. Fukuoka. 1976. Chemical and biochemical studies on carbohydrate esters. III. Antitumor activity of unsaturated fatty acids and their ester derivatives against Ehrlich ascites carcinoma. Chemical and Pharmaceutical Bulletin 24 (4):756–62.
   PubMed Web of Science ®Google Scholar
• Nishikawa, Y., K. Yoshimoto, M. Okada, T. Ikekawa, N. Abiko, and F. Fukuoka. 1977. Chemical and biochemical studies on carbohydrate esters. V. Anti Ehrlich ascites tumor effect and chromatographic behaviors of fatty acyl monoesters of sucrose and trehalose. Chemical and Pharmaceutical Bulletin 25 (7):1717–24.
   PubMed Web of Science ®Google Scholar
• Ono, M., C. Takamura, F. Sugita, C. Masuoka, H. Yoshimitsu, T. Ikeda, and T. Nohara. 2007. Two new steroid glycosides and a new sesquiterpenoid glycoside from the underground parts of Trillium kamtschaticum. Chemical and Pharmaceutical Bulletin 55 (4):551–6.
   PubMedGoogle Scholar
• Oscarson, S., and H. Ritzén. 1990. Syntheses of four fatty acid esters of sucrose found in type B trichomes of Solanum berthaultii Hawkes (wild potato), including the major component, 6-O-decanoyl-3,4-di-O-isobutyrylsucrose. Carbohydrate Research 205:61–70.
   PubMedGoogle Scholar
• Oscarson, S., and H. Ritzén. 1996. Synthesis of 6-O-acetyl-2,3,4-tri-O-[(S)-2-methylbutyryl]sucrose and the three regioisomers of 6-O acetyl-2,3,4-O-[(S)-2-methylbutyryl]-di-O-[(S)-3-methylpentanoyl]-sucrose, naturally occurring fatty acid esters of sucrose found in tobacco. Carbohydrate Research 284 (2):271–7.
   PubMedGoogle Scholar
• Park, K.-M., S. J. Lee, H. Yu, J.-Y. Park, H.-S. Jung, K. Kim, C. J. Lee, and P.-S. Chang. 2018. Hydrophilic and lipophilic characteristics of non-fatty acid moieties: Significant factors affecting antibacterial activity of lauric acid esters. Food Science and Biotechnology 27 (2):401–9.
   PubMed Web of Science ®Google Scholar
• Parker, D. L., C. D. Wilson, G. S. Puritch, and D. S. Almond. 2006. Wide spectrum insecticide and miticide composition. U.S. Patent No. 8,007,820 B2, filed September 14, 2006, and issued March 22, 2007. https://patents.google.com/patent/US8007820B2.
   Google Scholar
• de Paulo Farias, D., and M. G. dos Santos Gomes. 2020. COVID-19 outbreak: What should be done to avoid food shortages? Trends in Food Science and Technology 102:291–2.
   PubMed Web of Science ®Google Scholar
• Peterson, J. K., H. F. Harrison, and O. T. Chortyk. 1997. Effects of various synthetic sucrose esters on weed seed germination and crop growth: Structure–activity and dose-response relationships. Journal of Agricultural and Food Chemistry 45 (12):4833–7.
   Google Scholar
• Peterson, J. K., M. E. Snook, H. F. Harrison, and P. F. Mason. 1998. Isolation and structural identification of sucrose esters from corn spurrey (Spergula arvensis); inhibition of seed germination. Journal of Chemical Ecology 24 (11):1803–16.
   Google Scholar
• Petkova, N., D. Vassilev, R. Grudeva, Y. Tumbarski, I. Vasileva, M. Koleva, and P. Denev. 2017. “Green” synthesis of sucrose octaacetate and characterization of its physicochemical properties and antimicrobial activity. Chemical and Biochemical Engineering Quarterly 31 (4):395–402.
   Web of Science ®Google Scholar
• Pittarelli, G. W., J. G. Buta, J. W. Neal, W. R. Lusby, and R. M. Waters. 1992. Biological pesticide derived from Nicotiana plants. US Patent 5,260,281 A, filed May 1, 1992, and issued November 9, 1993. https://patents.google.com/patent/US5260281A
   Google Scholar
• Plat, T., and R. J. Linhardt. 2001. Syntheses and applications of sucrose-based esters. Journal of Surfactants and Detergents 4 (4):415–21.
   Google Scholar
• Poller, R. C., and A. Parkin. 1977. Organometallic derivatives of sucrose as pesticides. In Sucrochemistry. ACS symposium series, ed. J. L. Hickson, vol. 11, 145–58. Washington, DC: American Chemical Society. doi: 10.1021/bk-1977-0041.ch011.
   Google Scholar
• Puterka, G. J., W. Farone, T. Palmer, and A. Barrington. 2003. Structure-function relationships affecting the insecticidal and miticidal activity of sugar esters. Journal of Economic Entomology 96 (3):636–44.
   PubMed Web of Science ®Google Scholar
• Puterka, G. J., and R. F. Severson. 1995. Activity of sugar esters isolated from leaf trichomes of Nicotiana gossei to pear psylla (homoptera, psyllidae). Journal of Economic Entomology 88 (3):615–9.
   Google Scholar
• Salih, A. A., M. Baraibar, K. K. Mwangi, and G. Artan. 2020. Climate change and locust outbreak in East Africa. Nature Climate Change 10 (7):584–5.
   Web of Science ®Google Scholar
• Severson, R. F., R. F. Arrendale, O. T. Chortyk, C. R. Green, F. A. Thome, J. L. Stewart, and A. W. Johnson. 1985. Isolation and characterization of the sucrose esters of the cuticular waxes of green tobacco leaf. Journal of Agricultural and Food Chemistry 33 (5):870–5.
   Google Scholar
• Severson, R. F., R. F. Arrendale, O. T. Chortyk, A. W. Johnson, D. M. Jackson, G. R. Gwynn, J. F. Chaplin, and M. G. Stephenson. 1984. Quantitation of the major cuticular components from green leaf of different tobacco types. Journal of Agricultural and Food Chemistry 32 (3):566–70.
   Google Scholar
• Severson, R. F., D. M. Jackson, A. W. Johnson, V. A. Sisson, and M. G. Stephenson. 1991. Ovipositional behavior of tobacco budworm and tobacco hornworm: Effects of cuticular components from Nicotiana species. In Naturally occurring pest bioregulators. ACS symposium series, ed. P. Hedin, vol. 449, 264–77. Washington, DC: American Chemical Society. doi: 10.1021/bk-1991-0449.ch017.
   Google Scholar
• Severson, R. F., A. W. Johnson, and D. M. Jackson. 1985. Cuticular constituents of tobacco: Factors affecting their production and their role in insect and disease resistance and smoke quality. Recent Advances in Tobacco Science 11:105–74.
   Google Scholar
• Shao, S.-Y., Y.-G. Shi, Y. Wu, L.-Q. Bian, Y.-J. Zhu, X. Y. Huang, X.-Y. Huang, Y. Pan, L.-Y. Zeng, and R.-R. Zhang. 2018. Lipase-catalyzed synthesis of sucrose monolaurate and its antibacterial property and mode of action against four pathogenic bacteria. Molecules 23 (5):1118.
   PubMed Web of Science ®Google Scholar
• Shi, Y. G., J. R. Li, and Y. H. Chu. 2011. Enzyme-catalyzed regioselective synthesis of sucrose-based esters. Journal of Chemical Technology and Biotechnology 86 (12):1457–68.
   Web of Science ®Google Scholar
• Smith, S. M., and J. R. Stow. 1984. The potential of a sucrose ester coating material for improving the storage and shelf-life qualities of Cox’s Orange Pippin apples. Annals of Applied Biology 104 (2):383–91.
   Google Scholar
• Song, Y., L. Wen, J. Sun, W. Bai, R. Jiao, Y. Hu, X. Peng, Y. He, and S. Ou. 2016. Cytoprotective mechanism of ferulic acid against high glucose-induced oxidative stress in cardiomyocytes and hepatocytes. Food and Nutrition Research 60 (1):30323.
   PubMedGoogle Scholar
• Song, Z. J., S. J. Li, X. Chen, L. M. Liu, and Z. Q. Song. 2006. Synthesis of insecticidal sucrose esters. Forestry Studies in China 8 (3):26–9.
   Google Scholar
• Szűts, A., and P. Szabó-Révész. 2012. Sucrose esters as natural surfactants in drug delivery systems – A mini-review. International Journal of Pharmaceutics 433 (1–2):1–9.
   PubMedGoogle Scholar
• Teng, Y., S. G. Stewart, Y. W. Hai, X. Li, M. G. Banwell, and P. Lan. 2021. Sucrose fatty acid esters: Synthesis, emulsifying capacities, biological activities and structure-property profiles. Critical Reviews in Food Science and Nutrition 61 (19):3297–317.
   PubMedGoogle Scholar
• Thomas, L. V., E. A. Davies, J. Delves-Broughton, and J. W. T. Wimpenny. 1998. Synergist effect of sucrose fatty acid esters on nisin inhibition of gram-positive bacteria. Journal of Applied Microbiology 85 (6):1013–22.
   PubMed Web of Science ®Google Scholar
• 360 Research Reports. 2021. Global sucrose esters of fatty acids sales market report. Last Modified March 9, 2021. Accessed September 30, 2022. https://www.360researchreports.com/global-sucrose-esters-of-fatty-acids-sales-market-17622087.
   Google Scholar
• Tian, Y., W. Liu, Y. Lu, Y. Wang, X. Chen, S. Bai, Y. Zhao, T. He, F. Lao, Y. Shang, et al. 2016. Naturally occurring cinnamic acid sugar ester derivatives. Molecules 21 (10):1402.
   PubMedGoogle Scholar
• Toyang, N. J., M. A. Krause, R. M. Fairhurst, P. Tane, J. Bryant, and R. Verpoorte. 2013. Antiplasmodial activity of sesquiterpene lactones and a sucrose ester from Vernonia guineensis Benth. (Asteraceae). Journal of Ethnopharmacology 147 (3):618–21.
   PubMedGoogle Scholar
• Toyang, N. J., H. K. Wabo, E. N. Ateh, H. Davis, P. Tane, S. F. Kimbu, L. B. Sondengam, and J. Bryant. 2012. In vitro anti-prostate cancer and ex vivo antiangiogenic activity of Vernonia guineensis Benth. (Asteraceae) tuber extracts. Journal of Ethnopharmacology 141 (3):866–71.
   PubMedGoogle Scholar
• Vargas, J. A. M., J. O. Ortega, G. Metzker, J. E. Larrahondo, and M. Boscolo. 2020. Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds. Phytochemistry 177:112433.
   PubMedGoogle Scholar
• Vargas, J. A. M., J. O. Ortega, M. B. C. dos Santos, G. Metzker, E. Gomes, and M. Boscolo. 2020. A new synthetic methodology for pyridinic sucrose esters and their antibacterial effects against gram-positive and gram-negative strains. Carbohydrate Research 489:107957.
   PubMedGoogle Scholar
• Vargas, M., C. Pastor, A. Albors, A. Chiralt, and C. González-Martínez. 2008. Development of edible coatings for fresh fruits and vegetables: Possibilities and limitations. Fresh Produce 2 (2):32–40.
   Google Scholar
• Wadleigh, R. W., R. E. Perry, and P. J. Schroeder. 2005. Methods for using polyol esters to control pests. US Patent 8,093,183 B2, filed March 3, 2005, and issued September 8, 2005. https://patents.google.com/patent/US8093183B2.
   Google Scholar
• Wagh, A., S. Shen, F. A. Shen, C. D. Miller, and M. K. Walsh. 2012. Effect of lactose monolaurate on pathogenic and nonpathogenic bacteria. Applied and Environmental Microbiology 78 (9):3465–8.
   PubMed Web of Science ®Google Scholar
• Ye, R., and D. G. Hayes. 2014. Recent progress for lipase-catalysed synthesis of sugar fatty acid esters. Journal of Oil Palm Research 26:355–65.
   Web of Science ®Google Scholar
• Zafar, S., R. Ahmed, and R. Khan. 2016. Biotransformation: A green and efficient way of antioxidant synthesis. Free Radical Research 50 (9):939–48.
   PubMed Web of Science ®Google Scholar
• Zhang, C. R., W. Khan, J. Bakht, and M. G. Nair. 2016. New antiinflammatory sucrose esters in the natural sticky coating of tomatillo (Physalis philadelphica). An important culinary fruit. Food Chemistry 196:726–32.
   PubMedGoogle Scholar
• Zhang, X., F. Song, M. Taxipalati, W. Wei, and F. Feng. 2014. Comparative study of surface-active properties and antimicrobial activities of disaccharide monoesters. PLoS One. 9 (12):e114845.
   PubMed Web of Science ®Google Scholar
• Zhao, X., Y. Cui, P. Wu, P. Zhao, Q. Zhou, Z. Zhang, Y. Wang, and X. Zhang. 2020. Polygalae Radix: A review of its traditional uses, phytochemistry, pharmacology, toxicology, and pharmacokinetics. Fitoterapia 147 (104759) doi: 10.1016/j.fitote.2020.104759.
   Google Scholar
• Zhao, L., H. Zhang, T. Hao, and S. Li. 2015. In vitro antibacterial activities and mechanism of sugar fatty acid esters against five food-related bacteria. Food Chemistry 187:370–7.
   PubMed Web of Science ®Google Scholar
• Zhu, J.-P., M.-Y. Liang, Y.-R. Ma, L. V. White, M. G. Banwell, Y. Teng, and P. Lan. 2022. Enzymatic synthesis of an homologous series of long-and very long-chain sucrose esters and evaluation of their emulsifying and biological properties. Food Hydrocolloids 124:107149. doi: 10.1016/j.foodhyd.2021.107149.
   Google Scholar