{"title":"A NOTE ON THE BIOSYNTHESIS OF LONG-CHAIN 3-METHYL-2-ALKANONES FROM THE ROOT ESSENTIAL OIL OF INULA HELENIUM L. (ASTERACEAE)","authors":"Marija Gencic, N. Radulović","doi":"10.2298/FUPCT1502083G","DOIUrl":null,"url":null,"abstract":"A predominantly odd-numbered, Gaussian-like distribution of the relative amounts of 3-methyl-2-alkanones, from I. helenium root essential oil, was observed. This distribution pattern indicates that their biosynthesis is related to that of fatty acids and related compounds. Simple (non-branched) 2-alkanones also show an odd carbon number prevalence in plants and other organisms, and it was shown that their biosynthesis indeed proceeds via the acetate pathway. In this paper, we propose three possible biosynthetic pathways by which 3-methyl-2-alkanones could be formed in the plant tissues. The essential distinction between them lies in the way the branching methyl group is introduced. The Gaussian parameter σ for the observed distribution of these ketones could be interpreted as the error introduced by the first elongase enzyme system involved in the biosynthesis of fatty acid-derived compounds. BIOSINTEZA 3-METIL-2-ALKANONA DUGOG UGLJOVODONICNOG LANCA IZ ETARSKOG ULJA KORENA BILJNE VRSTE INULA HELENIUM L. (ASTERACEAE) 3-Metil-2-alkanoni dugog ugljovodonicnog lanca su nađeni u etarskom ulju korena biljne vrste I. helenium L. Uocena je Gausova raspodela njihovih relativnih kolicina, pri cemu su homolozi sa neparnim brojem C-atoma bili zastupljeniji. Ovakva raspodela ukazuje na to da njihova biosinteza protice veoma slicno kao i biosinteza masnih kiselina i srodnih jedinjenja. 2-Alkanoni sa neparnim brojem C-atoma su, takođe, zastupljeniji kod biljaka i ostalih organizama, a za njih je dokazano da zaista nastaju po gore pomenutom acetatnom biosintetskom putu. Imajuci sve ovo u vidu, predložili smo tri moguca biosintetska puta kojim bi 3-metil-2-alkanoni mogli nastati u biljnim tkivima. Osnovna razlika između predloženih puteva je u nacinu na koji se uvodi metil racva. Gausov parametar σ uocenih raspodela kolicina alkana bi se mogao posmatrati kao greska prvog enzimskog sistema elongaze koji ucestvuje u biosintezi masnih kiselina i jedinjenja koja se iz njih izvode. HIGHLIGHTS Homologous 3-methyl-2-alkanones (C 11 –C 19 ) detected in Inula helenium root essential oil had a predominantly odd-numbered Gaussian-like distribution. This specific distribution pattern indicates that their biosynthesis most likely proceeds via the acetate pathway. There are three possible biosynthetic pathways, with a different mode of introducing the methyl branch, by which 3-methyl-2-alkanones could be produced. The observed Gaussian parameter σ could be interpreted as the error of the first elongase enzyme system involved in the biosynthesis of fatty acid-derived compounds.","PeriodicalId":12248,"journal":{"name":"Facta Universitatis - Series: Physics, Chemistry and Technology","volume":"66 1","pages":"83-89"},"PeriodicalIF":0.0000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Facta Universitatis - Series: Physics, Chemistry and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2298/FUPCT1502083G","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
A predominantly odd-numbered, Gaussian-like distribution of the relative amounts of 3-methyl-2-alkanones, from I. helenium root essential oil, was observed. This distribution pattern indicates that their biosynthesis is related to that of fatty acids and related compounds. Simple (non-branched) 2-alkanones also show an odd carbon number prevalence in plants and other organisms, and it was shown that their biosynthesis indeed proceeds via the acetate pathway. In this paper, we propose three possible biosynthetic pathways by which 3-methyl-2-alkanones could be formed in the plant tissues. The essential distinction between them lies in the way the branching methyl group is introduced. The Gaussian parameter σ for the observed distribution of these ketones could be interpreted as the error introduced by the first elongase enzyme system involved in the biosynthesis of fatty acid-derived compounds. BIOSINTEZA 3-METIL-2-ALKANONA DUGOG UGLJOVODONICNOG LANCA IZ ETARSKOG ULJA KORENA BILJNE VRSTE INULA HELENIUM L. (ASTERACEAE) 3-Metil-2-alkanoni dugog ugljovodonicnog lanca su nađeni u etarskom ulju korena biljne vrste I. helenium L. Uocena je Gausova raspodela njihovih relativnih kolicina, pri cemu su homolozi sa neparnim brojem C-atoma bili zastupljeniji. Ovakva raspodela ukazuje na to da njihova biosinteza protice veoma slicno kao i biosinteza masnih kiselina i srodnih jedinjenja. 2-Alkanoni sa neparnim brojem C-atoma su, takođe, zastupljeniji kod biljaka i ostalih organizama, a za njih je dokazano da zaista nastaju po gore pomenutom acetatnom biosintetskom putu. Imajuci sve ovo u vidu, predložili smo tri moguca biosintetska puta kojim bi 3-metil-2-alkanoni mogli nastati u biljnim tkivima. Osnovna razlika između predloženih puteva je u nacinu na koji se uvodi metil racva. Gausov parametar σ uocenih raspodela kolicina alkana bi se mogao posmatrati kao greska prvog enzimskog sistema elongaze koji ucestvuje u biosintezi masnih kiselina i jedinjenja koja se iz njih izvode. HIGHLIGHTS Homologous 3-methyl-2-alkanones (C 11 –C 19 ) detected in Inula helenium root essential oil had a predominantly odd-numbered Gaussian-like distribution. This specific distribution pattern indicates that their biosynthesis most likely proceeds via the acetate pathway. There are three possible biosynthetic pathways, with a different mode of introducing the methyl branch, by which 3-methyl-2-alkanones could be produced. The observed Gaussian parameter σ could be interpreted as the error of the first elongase enzyme system involved in the biosynthesis of fatty acid-derived compounds.
结果表明,从荷叶根精油中提取的3-甲基-2-烷酮的相对含量呈奇数高斯分布。这种分布模式表明它们的生物合成与脂肪酸和相关化合物的生物合成有关。简单(非支链)2-烷酮在植物和其他生物中也显示出奇数碳数,并且表明它们的生物合成确实通过醋酸途径进行。本文提出了3-甲基-2-烷酮在植物组织中形成的三种可能的生物合成途径。它们之间的本质区别在于引入支甲基的方式。这些酮体分布的高斯参数σ可以解释为参与脂肪酸衍生化合物生物合成的第一延长酶系统所引入的误差。3-METIL-2-ALKANONA DUGOG UGLJOVODONICNOG LANCA IZ ETARSKOG ULJA KORENA BILJNE VRSTE INULA HELENIUM L. (ASTERACEAE) 3-Metil-2-alkanoni DUGOG UGLJOVODONICNOG LANCA su nađeni u etarskom ulju KORENA BILJNE VRSTE I. HELENIUM L. Uocena je Gausova raspodela njihovih相对于kolicina, pri cemu su homolozi sa neparnim brojem c - atomia bili zastupljeniji。在中国,有两种不同类型的植物,一种不同类型的植物,一种不同类型的植物,一种不同类型的植物。2 . alkanoni sa neparnim brojem - c - atomsu, takođe, zastupljeniji kod biljaka i ostali组织,aza njih je dokazano da zaista nastaju - 1现象:乙酰氨基生物碱。Imajuci sve ovu video, predložili smo tri mogca bioosintetska puta kojim bi 3- meil -2-alkanoni mogli nastati u biljnim tkivima。Osnovna razlika između predloženih puteva je u nacinu na koji se uvodi metiva。Gausov parametarσuocenih raspodela kolicina alkana bi se mogao posmatrati花王greska prvog enzimskog sistema elongaze koji ucestvuje u biosintezi masnih kiselina我jedinjenja koja se工业区njih izvode。结论:在菊根精油中检测到的同源3-甲基-2-烷酮(c11 - c19)以奇数高斯分布为主。这种特殊的分布模式表明它们的生物合成最有可能通过醋酸途径进行。有三种可能的生物合成途径,通过不同的方式引入甲基分支,可以生产3-甲基-2-烷酮。观察到的高斯参数σ可以解释为参与脂肪酸衍生化合物生物合成的第一延长酶系统的误差。