Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/28958
Title: Optimized analysis and quantification of glucosinolates from Camelina sativa seeds by reverse-phase liquid chromatography
Authors: Berhow, Mark A.
Glinski, Jan A.
Glensk, Michal
Vaughn, Steven F.
Isbell, Terry
Ayala-Diaz, Ivan
Marek, Laura
Gardner, Candice
Uludağ Üniversitesi/Veterinerlik Fakültesi/Biyokimya Anabilim Dalı.
Polat, Ümit
56235316900
Keywords: Agriculture
Camelina sativa L Cranz
Glucosinolates
HPLC analysis
Purification
Seed analysis
Oxidative stability
Vegetable-oils
Quality
Plant
Isothiocyanates
Purification
Performance
Tocopherol
Products
Meal
Animalia
Camelina
Camelina sativa
Linum usitatissimum
Chromatographic analysis
Liquid chromatography
Oils and fats
Plant extracts
Purification
Seed
Animal feed
Camelina
Countercurrent chromatography
Field trial
Glucosinolate contents
Glucosinolates
HPLC analysis
Ion exchange chromatography
Oil crops
Reverse phase chromatography
Reverse phase HPLC
Reverse phase liquid chromatography
Seed meal
Separation and purification
Biofuel
Cultivar
Dicotyledon
Ion chromatography
Liquid chromatography
Optimization
Plant extract
Purification
Seed
Separation
Vegetable oil
Derivatives
Issue Date: Apr-2013
Publisher: Elsevier
Citation: Berhow, M. A. vd. (2013). "Optimized analysis and quantification of glucosinolates from Camelina sativa seeds by reverse-phase liquid chromatography". Industrial Crops and Products, 43(1), 119-125.
Abstract: Gold-of-pleasure or false flax (Camelina sativa L Crantz) is being developed as an alternative oil crop for biodiesel and for food use. The seed meal, which contains three relatively unique glucosinolates, is being evaluated for approval for use as an ingredient in animal feeds and for other uses. The objective of this research was to develop reproducible methods for the isolation of large quantities of pure camelina glucosinolates (glucoarabin, glucocamelinin, and 11-(methylsulfinyl)-undecylglucosinolate) and develop efficient methods for quantifying these compounds. The separation and purification of the camelina glucosinolates were achieved using a combination of reverse phase chromatography, counter-current chromatography and ion exchange chromatography. An efficient reverse phase HPLC separation method was used to quantitate the glucosinolate content in camelina seed and plant extracts. The quanti ration methodology was used to measure glucosinolate levels in seeds from 30 cultivars grown in a U.S. field trial and measure glucosinolates levels in sprouted camelina seeds.
URI: https://doi.org/10.1016/j.indcrop.2012.07.018
https://www.sciencedirect.com/science/article/pii/S0926669012003871
http://hdl.handle.net/11452/28958
ISSN: 0926-6690
1872-633X
Appears in Collections:Scopus
Web of Science

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.