{"title":"印度东北部一些野生肉豆蔻的油脂化学潜力","authors":"Rubi Barman , Jadumoni Saikia , Prasanna Sarmah , Parthapratim Konwar , Siddhartha Proteem Saikia , Saikat Haldar , Dipanwita Banik","doi":"10.1016/j.bse.2024.104904","DOIUrl":null,"url":null,"abstract":"<div><div>The essential and fixed oils cover a vast arena of industrial usage, including flavour-fragrances, cosmetics, health-body care, biofuel and bioenergy. The species of Myristicaceae were traditionally used to prepare soaps and candles. The research focused on extracting and characterising the essential and fixed oils of Myristicaceae from Assam and adjoining region. The study found essential oil for the first time from vegetative parts of <em>Horsfieldia kingii</em> and <em>H. amygdalina</em> from NE India<em>.</em> GC-MS analysis exhibited nearly 47 compounds among <em>Horsfieldia kingii, H. amygdalina</em> and <em>Knema angustifolia</em>, having compositional similarity among the latter two. About 11 common and significant compounds identified were copaene (1.34–22.22%), β-caryophyllene (0.34–4.36%), caryophyllene oxide (0.82–50.43%), humulene epoxide II (1.21–5.67%), δ-cadinol (1.10–7.92%), epi-γ-eudesmol (3.03–10.83%), globulol (0.82–42.28%), viridiflorol (2.34–39.14%), β-elemene (0.47–18.62%), shyobunol (1.37–7.5%) and t-cadinol (1.29–4.46%). The volatiles with high area coverage were juniper camphor (70.85%), caryophyllene oxide (50.43%), globulol (42.28%), viridiflorol (39.14%), α-pinene (36.56%), and β-selinene (20.53%). The physicochemical parameters of fixed oils of kernel and mace of <em>H. amygdalina</em>, <em>H. kingii</em>, <em>K. angustifolia, K. linifolia</em> and <em>K. tenuinervia</em> for the first time showed the yield 6.10–44.35% with compositional abundance of myristic acid, methyl ester (20.87–86.1%), lauric acid, methyl ester (35.81–40.02%), oleic acid, methyl ester (30.2–47.45%), palmitic acid, methyl ester (19.16–37.9%), mostly the saturated fatty acids. Both essential and fixed oils of wild nutmegs depicted the commercial potential of wild biowaste for novel renewable source of biomarkers.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The oleochemical potential of some wild nutmegs from North East India\",\"authors\":\"Rubi Barman , Jadumoni Saikia , Prasanna Sarmah , Parthapratim Konwar , Siddhartha Proteem Saikia , Saikat Haldar , Dipanwita Banik\",\"doi\":\"10.1016/j.bse.2024.104904\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The essential and fixed oils cover a vast arena of industrial usage, including flavour-fragrances, cosmetics, health-body care, biofuel and bioenergy. The species of Myristicaceae were traditionally used to prepare soaps and candles. The research focused on extracting and characterising the essential and fixed oils of Myristicaceae from Assam and adjoining region. The study found essential oil for the first time from vegetative parts of <em>Horsfieldia kingii</em> and <em>H. amygdalina</em> from NE India<em>.</em> GC-MS analysis exhibited nearly 47 compounds among <em>Horsfieldia kingii, H. amygdalina</em> and <em>Knema angustifolia</em>, having compositional similarity among the latter two. About 11 common and significant compounds identified were copaene (1.34–22.22%), β-caryophyllene (0.34–4.36%), caryophyllene oxide (0.82–50.43%), humulene epoxide II (1.21–5.67%), δ-cadinol (1.10–7.92%), epi-γ-eudesmol (3.03–10.83%), globulol (0.82–42.28%), viridiflorol (2.34–39.14%), β-elemene (0.47–18.62%), shyobunol (1.37–7.5%) and t-cadinol (1.29–4.46%). The volatiles with high area coverage were juniper camphor (70.85%), caryophyllene oxide (50.43%), globulol (42.28%), viridiflorol (39.14%), α-pinene (36.56%), and β-selinene (20.53%). The physicochemical parameters of fixed oils of kernel and mace of <em>H. amygdalina</em>, <em>H. kingii</em>, <em>K. angustifolia, K. linifolia</em> and <em>K. tenuinervia</em> for the first time showed the yield 6.10–44.35% with compositional abundance of myristic acid, methyl ester (20.87–86.1%), lauric acid, methyl ester (35.81–40.02%), oleic acid, methyl ester (30.2–47.45%), palmitic acid, methyl ester (19.16–37.9%), mostly the saturated fatty acids. Both essential and fixed oils of wild nutmegs depicted the commercial potential of wild biowaste for novel renewable source of biomarkers.</div></div>\",\"PeriodicalId\":8799,\"journal\":{\"name\":\"Biochemical Systematics and Ecology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2024-10-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemical Systematics and Ecology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0305197824001224\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical Systematics and Ecology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0305197824001224","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
The oleochemical potential of some wild nutmegs from North East India
The essential and fixed oils cover a vast arena of industrial usage, including flavour-fragrances, cosmetics, health-body care, biofuel and bioenergy. The species of Myristicaceae were traditionally used to prepare soaps and candles. The research focused on extracting and characterising the essential and fixed oils of Myristicaceae from Assam and adjoining region. The study found essential oil for the first time from vegetative parts of Horsfieldia kingii and H. amygdalina from NE India. GC-MS analysis exhibited nearly 47 compounds among Horsfieldia kingii, H. amygdalina and Knema angustifolia, having compositional similarity among the latter two. About 11 common and significant compounds identified were copaene (1.34–22.22%), β-caryophyllene (0.34–4.36%), caryophyllene oxide (0.82–50.43%), humulene epoxide II (1.21–5.67%), δ-cadinol (1.10–7.92%), epi-γ-eudesmol (3.03–10.83%), globulol (0.82–42.28%), viridiflorol (2.34–39.14%), β-elemene (0.47–18.62%), shyobunol (1.37–7.5%) and t-cadinol (1.29–4.46%). The volatiles with high area coverage were juniper camphor (70.85%), caryophyllene oxide (50.43%), globulol (42.28%), viridiflorol (39.14%), α-pinene (36.56%), and β-selinene (20.53%). The physicochemical parameters of fixed oils of kernel and mace of H. amygdalina, H. kingii, K. angustifolia, K. linifolia and K. tenuinervia for the first time showed the yield 6.10–44.35% with compositional abundance of myristic acid, methyl ester (20.87–86.1%), lauric acid, methyl ester (35.81–40.02%), oleic acid, methyl ester (30.2–47.45%), palmitic acid, methyl ester (19.16–37.9%), mostly the saturated fatty acids. Both essential and fixed oils of wild nutmegs depicted the commercial potential of wild biowaste for novel renewable source of biomarkers.
期刊介绍:
Biochemical Systematics and Ecology is devoted to the publication of original papers and reviews, both submitted and invited, in two subject areas: I) the application of biochemistry to problems relating to systematic biology of organisms (biochemical systematics); II) the role of biochemistry in interactions between organisms or between an organism and its environment (biochemical ecology).
In the Biochemical Systematics subject area, comparative studies of the distribution of (secondary) metabolites within a wider taxon (e.g. genus or family) are welcome. Comparative studies, encompassing multiple accessions of each of the taxa within their distribution are particularly encouraged. Welcome are also studies combining classical chemosystematic studies (such as comparative HPLC-MS or GC-MS investigations) with (macro-) molecular phylogenetic studies. Studies that involve the comparative use of compounds to help differentiate among species such as adulterants or substitutes that illustrate the applied use of chemosystematics are welcome. In contrast, studies solely employing macromolecular phylogenetic techniques (gene sequences, RAPD studies etc.) will be considered out of scope. Discouraged are manuscripts that report known or new compounds from a single source taxon without addressing a systematic hypothesis. Also considered out of scope are studies using outdated and hard to reproduce macromolecular techniques such as RAPDs in combination with standard chemosystematic techniques such as GC-FID and GC-MS.