R. C. Ranveer, A. S. Nanadane, P. M. Ganorkar, A. Sahoo
{"title":"酶辅助提取枸杞果皮花青素","authors":"R. C. Ranveer, A. S. Nanadane, P. M. Ganorkar, A. Sahoo","doi":"10.9734/ejnfs/2020/v12i1030309","DOIUrl":null,"url":null,"abstract":"Background: The kokum rind consists of high amount of anthocyanin. The traditional methods are not capable to extract anthocyanin completely. \nAims: The present study was focused on the optimization of enzyme pretreatment for extraction of anthocyanin from Kokum rind. \nMethodology: A central composite design was used to optimize the enzyme-assisted extraction of anthocyanin from the Kokum rinds. Kokum rinds was pretreated with food-grade pectinase and cellulase enzymes separately and then subjected to acidified ethanol extraction. The factors investigated included enzyme concentration (0 – 2%), Incubation time (1-5 h) and pretreatment temperature (15–55ºC). \nResults: Overall, 107.17- to 63.71 - fold increase in anthocyanin recovery when treated with pectinase and cellulase, respectively was observed compared to the untreated rinds. From a response surface analysis of the data, a second-degree polynomial equation was developed which provided the following optimal extraction conditions i.e. enzyme concentration 0.5%, Incubation time 2.0h and temperature 35ºC for pectinase pretreatment. Whereas, in case of cellulase the optimum conditions was enzyme concentration 1.42%, Incubation time 4.0h and temperature 32ºC. The obtained results strongly support the idea of using cell-wall degrading enzymes as an effective means for recovering anthocyanin from Kokum rinds. ","PeriodicalId":11994,"journal":{"name":"European Journal of Nutrition & Food Safety","volume":"37 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enzyme-Assisted Extraction of Anthocyanin from Kokum (Garcinia indica Choisy) Rinds\",\"authors\":\"R. C. Ranveer, A. S. Nanadane, P. M. Ganorkar, A. Sahoo\",\"doi\":\"10.9734/ejnfs/2020/v12i1030309\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: The kokum rind consists of high amount of anthocyanin. The traditional methods are not capable to extract anthocyanin completely. \\nAims: The present study was focused on the optimization of enzyme pretreatment for extraction of anthocyanin from Kokum rind. \\nMethodology: A central composite design was used to optimize the enzyme-assisted extraction of anthocyanin from the Kokum rinds. Kokum rinds was pretreated with food-grade pectinase and cellulase enzymes separately and then subjected to acidified ethanol extraction. The factors investigated included enzyme concentration (0 – 2%), Incubation time (1-5 h) and pretreatment temperature (15–55ºC). \\nResults: Overall, 107.17- to 63.71 - fold increase in anthocyanin recovery when treated with pectinase and cellulase, respectively was observed compared to the untreated rinds. From a response surface analysis of the data, a second-degree polynomial equation was developed which provided the following optimal extraction conditions i.e. enzyme concentration 0.5%, Incubation time 2.0h and temperature 35ºC for pectinase pretreatment. Whereas, in case of cellulase the optimum conditions was enzyme concentration 1.42%, Incubation time 4.0h and temperature 32ºC. The obtained results strongly support the idea of using cell-wall degrading enzymes as an effective means for recovering anthocyanin from Kokum rinds. \",\"PeriodicalId\":11994,\"journal\":{\"name\":\"European Journal of Nutrition & Food Safety\",\"volume\":\"37 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-11-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Nutrition & Food Safety\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.9734/ejnfs/2020/v12i1030309\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Nutrition & Food Safety","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/ejnfs/2020/v12i1030309","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Enzyme-Assisted Extraction of Anthocyanin from Kokum (Garcinia indica Choisy) Rinds
Background: The kokum rind consists of high amount of anthocyanin. The traditional methods are not capable to extract anthocyanin completely.
Aims: The present study was focused on the optimization of enzyme pretreatment for extraction of anthocyanin from Kokum rind.
Methodology: A central composite design was used to optimize the enzyme-assisted extraction of anthocyanin from the Kokum rinds. Kokum rinds was pretreated with food-grade pectinase and cellulase enzymes separately and then subjected to acidified ethanol extraction. The factors investigated included enzyme concentration (0 – 2%), Incubation time (1-5 h) and pretreatment temperature (15–55ºC).
Results: Overall, 107.17- to 63.71 - fold increase in anthocyanin recovery when treated with pectinase and cellulase, respectively was observed compared to the untreated rinds. From a response surface analysis of the data, a second-degree polynomial equation was developed which provided the following optimal extraction conditions i.e. enzyme concentration 0.5%, Incubation time 2.0h and temperature 35ºC for pectinase pretreatment. Whereas, in case of cellulase the optimum conditions was enzyme concentration 1.42%, Incubation time 4.0h and temperature 32ºC. The obtained results strongly support the idea of using cell-wall degrading enzymes as an effective means for recovering anthocyanin from Kokum rinds.