Selection of Direct Transesterification as the Preferred Method for Assay of Fatty Acid Content of Microalgae

被引:213
作者
Griffiths, M. J. [1 ]
van Hille, R. P. [1 ]
Harrison, S. T. L. [1 ]
机构
[1] Univ Cape Town, Ctr Bioproc Engn Res CeBER, ZA-7701 Cape Town, South Africa
基金
新加坡国家研究基金会;
关键词
Direct transesterification; Fatty acid; Lipid; Microalgae; Sodium methoxide; BF3; methanol; Chlorella; Scenedesmus; Nannochloropsis;
D O I
10.1007/s11745-010-3468-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Assays for total lipid content in microalgae are usually based on the Folch or the Bligh and Dyer methods of solvent extraction followed by quantification either gravimetrically or by chromatography. Direct transesterification (DT) is a method of converting saponifiable lipids in situ directly to fatty acid methyl esters which can be quantified by gas chromatography (GC). This eliminates the extraction step and results in a rapid, one-step procedure applicable to small samples. This study compared the effectiveness of DT in quantifying the total fatty acid content in three species of microalgae to extraction using the Folch, the Bligh and Dyer and the Smedes and Askland methods, followed by transesterification and GC. The use of two catalysts in sequence, as well as the effect of reaction water content on the efficiency of DT were investigated. The Folch method was the most effective of the extraction methods tested, but comparison with DT illustrated that all extraction methods were incomplete. Higher levels of fatty acid in the cells were obtained with DT in comparison with the extraction-transesterification methods. A combination of acidic and basic transesterification catalysts was more effective than each individually when the sample contained water. The two-catalyst reaction was insensitive to water up to 10% of total reaction volume. DT proved a convenient and more accurate method than the extraction techniques for quantifying total fatty acid content in microalgae.
引用
收藏
页码:1053 / 1060
页数:8
相关论文
共 37 条
[1]   CLASSIFICATION OF MICROORGANISMS BY ANALYSIS OF CHEMICAL COMPOSITION .1. FEASIBILITY OF UTILIZING GAS CHROMATOGRAPHY [J].
ABEL, K ;
DESCHMER.H ;
PETERSON, JI .
JOURNAL OF BACTERIOLOGY, 1963, 85 (05) :1039-&
[2]   Commercial developments in microalgal biotechnology [J].
Apt, KE ;
Behrens, PW .
JOURNAL OF PHYCOLOGY, 1999, 35 (02) :215-226
[3]   Optimization of Fatty Acid Determination in Selected Fish and Microalgal Oils [J].
Armenta, Roberto E. ;
Scott, Spencer D. ;
Burja, Adam M. ;
Radianingtyas, Helia ;
Barrow, Colin J. .
CHROMATOGRAPHIA, 2009, 70 (3-4) :629-636
[4]  
BENAMOTZ A, 1985, J PHYCOL, V21, P72
[5]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[6]   At-line gas chromatographic-mass spectrometric analysis of fatty acid profiles of green microalgae using a direct thermal desorption interface [J].
Blokker, P ;
Pel, R ;
Akoto, L ;
Brinkman, UAT ;
Vreuls, RJJ .
JOURNAL OF CHROMATOGRAPHY A, 2002, 959 (1-2) :191-201
[7]   Development in lipid analysis:: Some new extraction techniques and in situ transesterification [J].
Carrapiso, AI ;
García, C .
LIPIDS, 2000, 35 (11) :1167-1177
[8]   Metabolic relationships between macro- and micronutrients, and the eicosapentaenoic acid and docosahexaenoic acid contents of Pavlova lutheri [J].
Carvalho, AP ;
Pontes, I ;
Gaspar, H ;
Malcata, FX .
ENZYME AND MICROBIAL TECHNOLOGY, 2006, 38 (3-4) :358-366
[9]  
FAJARDO AR, 2007, LIPID FETT, V2, P120
[10]  
FOLCH J, 1957, J BIOL CHEM, V226, P497