Groundnuts from 16 Arachis hypogaea L. cultivars were found to contain oil in the range of 43 to

50%. Gas-liquid chromatographic analysis of the oil fatty acid methyl esters revealed the occurrence of

palmitic (12.22 to 13.30%), stearic (3.17 to 3.67%), oleic (37.94 to 41.90%) linoleic (34.59 to 37.51%),

arachidic (1.63 to 1.85%) eicosaenoic (0.99 to 1.22%), behenic (3.24 to 4.36%), and lignoceric (1.08 to

1.44%) as the major fatty acids. Cultivars Tainang 7, Kidang and Alabama were high in oil content and

contained relatively low levels of behenic acid and a high oleic/linoleic acid ratio in their oil

Berry, Shiv K.

Universiti Putra Malaysia Institutional Repository

Pertanika 5(1), 20-24 (1982)Fatty Acid Composition of 16 Groundnut (Arachis hypogaea, L.)Cultivars grown under Malaysian ConditionsSHIV K. BERRYDepartment ofFood Science, Faculty ofFood Science and Technology, Universiti Pertanian Malaysia,Serdang, Selangor, Malaysia.Key words: Groundnut cultivars; Arachis hypogaea; oil; fatty acids; gas chromatography, oleic/linoleicacid ratio.RINGKASANEnambelas kultivar kacang tanah Arachis hypogaeaL. telah didapati mengandungi minyak di dalamjulat 43 hingga 50 peratus. Penganalisaan kromatograpi gas-cecair akan ester-ester metil asid lemak telahdijalankan. Analisa ini telah menunjukkan adanya asid-asid major seperti palmitik (12.22 hingga 13.30%),stearik (3.17 hingga 3.67%) oleik (37.94 hingga 41.90%) linoleik (34.59 hingga 37.51%), arachidik (1.63hingga 1.85%), eicosaenoik (0.99 hingga 1.22%), behenik (3.24 hingga 4.36%) dan lignocerik (1.08 hingga1.44%). Kultivar-kultivar Tainang 7, Kidang dan Alabama telah didapati mempunyai kandungan minyakyang tinggi dan paras asid behenik yang rendah serta nisbah asid oleikjlinoleik yang tinggi di dalam minyakmereka.SUMMARYGroundnuts from 16 Arachis hypogaea L. cultivars were found to contain oil in the range of 43 to50%. Gas-liquid chromatographic analysis of the oil fatty acid methyl esters revealed the occurrence ofpalmitic (12.22 to 13.30%), stearic (3.17 to 3.67%), oleic (37.94 to 41.90%) linoleic (34.59 to 37.51%),arachidic (1.63 to 1.85%) eicosaenoic (0.99 to 1.22%), behenic (3.24 to 4.36%), and lignoceric (1.08 to1.44%) as the major fatty acids. Cultivars Tainang 7, Kidang and Alabama were high in oil content andcontained relatively low levels of behenic acid and a high oleic/linoleic acid ratio in their oil.INlRODUCTIONPlant breeders, generally, concentrate theirefforts on evolving species/varieties that are highyielding and pest resistant. However, such effortstend to attach secondary importance to the com-positional and nutritional aspects of the finalcrop. In the case of oil seed crops, it would bedesirable to evolve a variety that has not onlyhigh oil content but also a nutritionally desirablefatty acid composition.Much effort has been given to the improve-ment of groundnut (Arachis hypogaea L.) varietiesthrough breeding programmes all over the world.The parameters that have been inve&tigated includeclimate, irrigation, fertilizer, soil, location, etc. andtheir influence on the yield, protein and oil content,as well as the fatty acid and amino acid composition(Brown et al., 1975; Young et al., 1974; Downeyand McGregor, 1976). The fatty acid compositionKey to author's name: S.K. Berry.20of the oil in seed crops plays an important role indetermining the functional properties, shelf-life,nutritional value and flavour of the food productsderived from them (Lea, 1962). The addition tofood products of groundnut oil or oil-containingmeal COUld, therefore, alter such characteristics inthe final product. Changes in flavour quality maybe caused by the development of oxidative ranci-dity which has been related, at least in part, tohigh linoleic acid content of the oil (Fore et al.,1953). On the other hand, a reasonable proportionof linoleic acid is essential in nutritional terms.The evidence that long-chain fatty acids, e.g.arachidic and behenic, in groundnut oil may beimplicated in heart disease has been noted(Nutrition Foundation, Inc. 1972; Kies et al.,1978; Kritchevsky et aI., 1971), but such long-chain fatty acids also have commercial importancesince they assist in emulsification and stabilizationof products such as peanut butter.S.K. BERRYIn Malaysia, research is in progress to selectand identify groundnut varieties that are highyielding and pest resistant under local conditions(Lim, E.S. Personal Communications, 1980/81).The oil and protein contents of the nuts and thefatty acid composition of the oil need also to beinvestigated, as these vary with the variety orcultivar. This paper reports the fatty acid composi-tion of the oil from 16 groundnut cultivars grownunder the Malaysian conditions.MATERIALS AND MElHODSMaterialsThe groundnut samples used in this experimentwere obtained through the Department of Horti-cUlture, Faculty of Agriculture, Universiti PertanianMalaysia. All cultivars were grown at the Experi-mental Farm under similar conditions and receivedthe same post harvest treatments. The solvents andreagents used in the analysis were of analyticalgrade. Methyl fatty acid ester reference standardsaJ ~ N~ N.. N,;were purchased from Sigma Chemical Company,St. Louis, MO, USA.Ex traction of OilSamples of groundnut (10-15 g) inclu ding theseed coat were randomly divided into two portionsand ground to a fine meal. The meal was transferredto a Whatman thimble, the pestle and mortar wererinsed with petroleum ether (b.p. 40-60° C)the washings were poured into the thimble in theSoxhlet apparatus. Extraction with petroleum etherwas carried out for 16 hours in a fume chamber.The oil was recovered by evaporating the petroleumether under vacuum in a rotary evap orator at 45° C.Transesterification of the OilThe oil fatty acid methyl esters were preparedby transmethylation using 0.5 Msodium methoxidein methanol as described by Timms (1978).Gas Liquid Chromatography (GLC)The oil fatty acid methyl esters obtainedfrom each replicate sample were analysed using aC'l0l .'"'~~'"~N'" A~..J\A NM'"..\J ~TIME (MIN)Fig. 1. A typical gas-liquid chromatogram of groundnut oil fatty acid methyl easters. Column: Diethyleneglycol succinate, sample size: 0.8 /11 (5% in petroleum ether).21FArrY ACID COMPOSITION OF 16 GROUNDNUTCULTIVARSPye Unicam, series 204, gas chromatograph. Thechromatograph operating parameters have beendescribed previously (Berry, 1980). A typicalgas liquid chromatogram of groundnut oil fattYacid methyl esters is depicted in Figure 1. Peakidentification and area percentage calculationtechniques have been reported earlier (Berry,1980).The results were su bjected to the analysisof variance and least significant difference test(LSD) to ascertain the variability in oil contentand fatty acid composition.RESULTS AND DISCUSSIONThe groundnut samples employed in thisinvestigation were not graded for size as theamount of samples available for analysis was only10-15 g. Consequently, some samples containedmore of underdeveloped, small-sized and wrinkledkernels than the others. This variability may havecon tributed to the differences in oil content andfatty acid composition of the oil in differentcultivars.The mean value of the oil content of 16groundnut cultivars varied between 43 to 50% ona dry weight basis with a coefficient of variationof 2.38 (Table 1). The highest amount of oiloccurred in groundnut cultivars Kidang andTainang 7, both of Spanish type. The LSD teston the oil content data indicated significantdifferences in oil content for cultivars Kidang,Tainang 7 and Alabama when compared withcultivars Nan Gai 60,47-5, CESIOl, Kuala BrangK- 2, Banting, CES 102, Red Indonesian andSungai Sipu t Local.Fatty Acid CompositionTable 1 shows the differences in fatty acidcomposition of the oil from 16 groundnut cultivars.The differences in methyl fatty acid ester values (%)for palmitic (16: 0), stearic (18:0), Oleic (18: 1),linoleic (18: 2), eicosaenoic (20: 1), behenic (22: 0)and lignoceric (24: 0) in the oil of these cultivarswere significant at 5% level. For palmitoleic (16: 1)and arachidic (20: 0) fatty acids, on the otherhand the values varied insignificantly from oneculti~ar to another. Oleate and linoleate togetherconstitu ted 74-76% of the total fatty acids;a desirable nutritional trait. However, higherunsaturation in an oil affects seed stability andlowers the shelf-life of such oil-derived products(Lea, 1962).22The ratio between 18: I and 18: 2 fattyacid values varied amongst the cultivars with acoefficient of variation of 4.44. The ratio of18: 1/18: 2 in the' oil of cultivars Alabama andKidang was significantly different (5% level)from that of cultivars CES 101, Kuala BrangK-2, CES 102, Matjam, Gadjah and F-334-33,while the remaining cultivars were relativelyinsensitive to these differences. The role of the18: 1/18:2 ratio in groundnut oils has beenemphasized in controlling the shelf-life of theproducts (W orthington et al., 1972; Young et al.,1974). The higher this ratio, the higher is the oilstability and the longer is the shelf-life of roastedand other groundnut products. Manufacturers mayincrease the 18: 1/18:2 ratio by blending differentvarieti€ls of groundnuts to prepare products such aspeanut butter with improved texture, flavour andstability (Worthington and Hammons, 1971). Forthis purpose, locally produced cultivars Alabamaand Kidang may prove more suitable.The results in Table 1 also indicate that thepercentage of behenate in the oil of cultivarsTainang 7 and Kidang differed significantlyfrom that of the cultivars Nan Gai 60, 47- 5, RedIndonesian, CES 102, SK 28, Sungai Siput Local,V-13, Kuala Brang K-2, CES 101, Gadjah, Bantingand F334-33. The percentage of arachidate wasrelatively insensitive to cultivar differences. Thetotal percentage of arachidate plus behenate washighest in the cultivar Nan Gai 60 and the lowestin cultivar Tainang 7, followed by cultivars Kidangand Alabama. A low level of arachidic and behenicacids in groundnut oil is considered desirableas these fatty acids have been associated withatherogenicity of the groundnut oils (Kritchevskyet al., 1971; Nutrition Foundation, Inc., 1973;Kies et aI., 1978). Kritchevsky et aI., (1981) havefurther shown that groundnut oils of differentorigins exhibit different levels of atherogenicityin rabbits. They attributed these differencesto the manner of distribution of these fatty acidson the triglyceride molecules in various groundnutoils. The possibility of occurrence in these oilsof other unknown factor(s) with atherogenicproperties cannot be ruled out. However, thepotential health hazard of these two fatty acidsshould be considered in the evaluation of differentgroundnut varieties.These observations on oil content and fattyacid composition of the variousgroundnutvarietiessuggest that cultivars Tainang 7, Kidang andAlabama may prove more promising for furthermultiplication and for commercial purposes.TABLE 1The oil Content and Fatty Acid Composition of 16 Groundnut CultivarsaOil Methyl Fatty Acid Esters (Mean of Area %) 18:1/ TotalCultivar %16:0b18:2 20:0 + 22:0DB 16:1 18:0 18:1 18:2 20:0 20:1 22:0 24:0 RatioNan Gai 60 43.43 12.98 0.12 3.65 39.09 35.35 1.85 1.10 4.36 1.41 1.11 6.2147 - 5 44.36 12.97 0.11 3.38 39.27 35.85 1.71 1.15 4.06 1.42 1.10 5.77CES 101 45.56 13.30 0.11 3.56 38.60 36.72 1.69 1.04 3.62 1.26 1.05 5.31Kuala Brang K-2 45.77 13.02 0.13 3.42 38.55 36.81 1.85 1.16 3.66 1.27 1.05 5.50Banting 45.96 12.58 0.11 3.23 40.67 35.67 1.67 1.13 3.59 1.27 1.15 5.26CES 102 45.97 13.17 0.12 3.38 37.94 37.03 1.76 1.16 3.96 1.37 1.03 5.72Red Indonesian 46.20 12.53 0.12 3.17 39.80 35.94 1.67 1.22 4.04 1.44 1.11 5.71Sungai Siput Local 46.41 13.12 0.12 3.23 38.87 35.62 1.66 1.15 3.70 1.36 1.12 5.35 CI.lN ~UJ V-13 (Cheek) 47.08 12.88 0.11 3.56 39.76 35.91 1.73 1.04 3.68 1.19 1.11 5.41IJ:jMatjam 47.18 12.93 0.11 3.67 39.42 36.43 1.69 0.97 3.46 1.15 1.09 5.15 tTl::eGadjah 47.97 13.13 0.11 3.56 38.65 37.00 1.70 1.06 3.61 1.11 1.05 5.31 ::e><:SK 28 48.07 13.01 0.11 3.59 39.45 35.91 1.77 1.08 3.74 1.25 1.10 5.51F-334-33 48.21 13.17 0.11 3.46 38.18 37.51 1.68 1.04 3.59 1.18 1.02 5.27Alabama 48.98 12.22 0.12 3.31 41.90 34.59 1.63 1.13 3.51 1.41 1.22 5.14Tainang 7 49.88 12.84 0.11 3.66 41.32 35.05 1.64 0.99 3.24 1.08 1.18 4.88Kidang 50.24 12.60 0.11 3.55 41.67 34.73 1.68 1.06 3.40 1.13 1.20 5.08Coefficient of Variation 2.38 1.68 10.40 4.02 2.34 1.96 4.27 5.10 3.86 4.99 4.44 2.88L.S.D.,5% 2.38 0.43 0.02 0.21 1.98 1.51 0.16 0.12 0.30 0.13 0.10 0.30L.S.D.,l% 3.29 0.59 0.03 0.29 2.73 2.08 0.22 0.16 0.42 0.19 0.14 0.42~ ~~: ~:~~~s~~~~~U~:~::d:ype), Spanish type.DB = Dry basisFATTY ACID COMPOSITION OF 16 GROUNDNUT CULTIVARSCONCLUSIONThere are numerous variables includingclimate, location, soil, irrigation, fertilizer, postharvest processing, storage, etc. that may affectthe composition of groundnuts. The presentinvestigation did not incorporate any of thesevariables in the experimental design. Nevertheless,these preliminary studies on the differences inoil content and oil fatty acid composition of16 groundnut varieties support the need forselection and development of commercial varietieswith desired levels of stability and nutritionalcharacteristics.ACKNOWLEDGMENTSThe author is grateful to Dr. Lim Eng Siong,Head Department of Agronomy and Horticulture,for the supply of groundnut samples, and toDr. Yap Thoo Chye for assistance in the statisticalanalysis of data.REFERENCESBERRY, S.K. (1980): The fatty acid composition andcyclopropene fatty acid content of the maturingOkra (Hibiscus esculentus 1.) fruits. Pertanika 3,82-86.BROWN D.F. CATER, C.M., MATTIL, K.F. andDARROCH, J.G. (1975): Effect of varien:, growinglocation and their influence on the fatty aCId compo-sition of peanuts. 1. Food Sci. 40,1055-1060.DOWNEY, RK. and McGREGOR, DJ. (1976): "Breedingfor modified fatty acid composition ': In CC!mmen-taries in Plant Science, pp. 153-169. (Ed. SmIth, H.).Oxford. Academic Press.FORE, S.P., MORRIS, N.J., MACK, C.H., FREEMAN,A.F. and BRICKFORD, W.G. (1953): Factorsaffecting the stability of crude oils of 16 varietiesof peanuts. 1. Am. Oil Chem. Soc. 30,298-301.24KIES, C., LOPEZ-RICO, M.E., FOX, H.M., STANEK,K.M. and CHAN, A. (1978): Bloodserum lipidpatterns of adolescent boys fed corn oil, peanut oilor safflower oil 1. Food Sci 43,1293-1296.KRITCHEVSKY, D., TEPPER, S.A., VESSELINOVITCH,D. and WISSLER, R.W. (1971): Cholesterol vehiclein experimental atherosclerosis. 11. Peanut oil.Atherosclerosis 14, 53-64.KRITCHEVSKY, D., TEPPER, S.A., SCOTT, D.A.,KLURFELD, D.M., VESSELINOVITCH, D. andWISSLER, R.W. (1981): Cholesterol vehicle inexperimental atherosclerosis. 18. Comparison ofNorth American, African and South Americanpeanut oils. Atherosclerosis 38, 291-299.LEA, C.H. (1962): "The oxidative deterioration offood lipids" In Symposium on Food: Lipids andTheir Oxidation, pp. 3-28 (Ed. Schultz, H. W.; Day,E.A. and Sinnhuber, RO.). Westport, Connecticut:The AVI Publishing Company, Inc.NUTRITION FOUNDATION, INC. (1973): Atherogeni-city of peanut oil in the rabbit. Nutr. Rev. 30, 70-72.TIMMS, R.E. (1978): Artefact peaks in the preparationand gas-liquid chromatographic determination ofmethyl esters. Aust. J. Dairy Technol. 33, 4-6.WORTHINGTON, R.E. and HAMMONS, R.O. (1971):Genotype variation in fatty acid composition andstability of Arachis hypogaea 1. oil. Oleagineux26, 695-700.WORTHINGTON, RE., HAMMONS, RO. and ALLISON,J.R. (1972): Varietal differences and seasonal effectson fatty acid composition and stability of oil from82 peanut genotypes. 1. Agric. Food Chem. 20727-730. 'YOUNG, C.T., WORTHINGTON, R.E., HAMMONS,R.O., MATLOCK, R.S., WALLER, G.R. andMORRISON, R.D. (1974): Fatty acid compositionof Spanish peanut oils as influenced by plantinglocation, soil moisture conditions, variety and season.1. Am. Oil Chem. Soc. 51,312-315.(Received 30 November 1981)

Fatty Acid Composition of 16 Groundnut (Arachis hypogaea, L.)

Cultivars grown under Malaysian Conditions

http://psasir.upm.edu.my/2150/1/Fatty_Acid_Composition_of_16_Groundnut_%28Arachis_hypogaea%2C_L.%29.pdf

Fatty Acid Composition of 16 Groundnut (Arachis hypogaea, L.) Cultivars grown under Malaysian Conditions

Abstract

Similar works

Full text

Available Versions

Universiti Putra Malaysia Institutional Repository