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Koziol, M.J. 1993. Quinoa: A potential new oil crop.
p. 328-336. In: J. Janick and J.E. Simon (eds.), New crops. Wiley, New
York.
Quinoa: A Potential New Oil Crop*
Michael J. Koziol
- POTENTIAL OF QUINOA
- Maize Oil Content and Yields
- Quinoa Oil Content and Yield
- Oil Composition
- BY-PRODUCTS OF QUINOA OIL PRODUCTION
- Saponins
- Oil Press Cake as a Dietary Supplement
- Carbohydrate Cream Substitute
- CONCLUSIONS
- REFERENCES
- Table 1
- Table 2
- Table 3
- Table 4
- Table 5
- Table 6
- Table 7
Quinoa (Chenopodium quinoa Willd.) is an Andean pseudocereal grain about
1.0 mm thick which ranges in diameter from 1.0 to 2.5 mm and in seed weight
from 1.9 to 4.3 g/1000 seeds (Alvarez et al. 1990). From earlier
investigations (White et al. 1955) to more recent reviews (Coulter and Lorenz
1990; Galwey et al. 1990), attention has focussed primarily on the content and
quality of the protein in quinoa. This absorbing interest in quinoa's profile
of essential amino acids has completely overshadowed another equally important
nutritional characteristic of the grain when compared with cereals, namely a
relatively high content of an oil which is rich in the essential fatty acids,
linoleate and linolenate (Koziol 1990a). (As arachidonic acid can be
synthesized from linoleic acid it will not here be considered as essential.)
The use of non-traditional oil crops, such as maize, as sources of edible
vegetable oils depends partially on their oil content and composition but more
importantly, on the commercialization of other major products derived from the
grain; oil production is best viewed as a byproduct in such cases. Thus, as
early as 1943, Jamieson stated: "Were it not for the fact that in the
preparation of hominy, starch, glucose, and other corn products, the germ is
almost completely separated from the rest of the kernel, corn oil would not
have become an important commercial product." Production of maize oil
increased proportionally with that of high-fructose corn syrup, and its
consumption has been boosted by an increasing public awareness of the
importance of polyunsaturated fats in the diet (Leibovitz and Ruckenstein
1983). Worldwide, the production of maize oil increased from 0.4 million t in
1965 to 1.0 million t in 1985, with a further increase to 1.5 million t
predicted by 1995 (Gunstone 1989). The production of maize oil as a
commercially viable byproduct serves as an appropriate model with which to
compare the potential of quinoa as a new oil source, with special emphasis on
Ecuadorian data.
Maize cultivated in the United States contains 3 to 4% oil (Mounts and Anderson
1983). The germ, which accounts for 5 to 14% of the weight of a maize kernel
(Lásztity 1984; Patterson 1989; Alexander 1989) contains about 85% of
the oil (Mounts and Anderson 1983). In the starch industry, the maize germ as
removed by the wet degermination (milling) process and presented for oil
extraction contains about 50% oil, as opposed to the 10 to 24% oil available in
germs removed by the dry process used in the production of hominy, grits, and
corn flakes (Leibovitz and Ruckenstein 1983).
Breeding programs for maize with a higher oil content have successfully
produced hybrids that have 6 to 8% oil with yields equivalent to those of other
commercial cultivars (Weber 1983). Hybrids with higher oil contents tend to
have lower yields in terms of tonnage per hectare; for example, within 22
cycles the oil content of 'Alexho Synthetic' was increased from 6.2 to 12.9%,
but the yield of the maize was reduced from 8.50 to 5.69 t/ha (Alexander 1989).
Given the higher oil content, oil yield per hectare actually increased from
0.53 to 0.73 t/ha. Increases in oil production, however, are accompanied by
increases in germ sizes and by decreases in grain and endosperm weight and
hence in starch production (Weber 1983; Alexander 1989). Despite the successes
of the maize breeders, the only inducement for farmers to cultivate the higher
oil content maize for milling up until the 1980s was special contracting (Weber
1983). More recently, the increased production of high-fructose sugars in the
United States suggests that higher oil content maize might not be welcome by
the wet millers, even though the value of maize oil is at least three times
higher than that of the corn starch (Alexander 1989). Some of the dry milling
processes cause excessive damage to the larger embryos of the higher oil
content maize resulting not only in contamination of the endosperm by oil but
also in the release of lipolytic enzymes from the embryo which can accelerate
rancidity. The future of the higher oil containing hybrids of maize depends
upon three factors: (1) a reassessment of the value of maize oil as a byproduct
in the production of other maize products; (2) the costs of modifying existing
processes and equipment to deal with the changes in the morphology of the
kernels; and (3) the productivity of the new hybrids in terms of yield per
hectare.
On a fresh weight basis quinoa shows an oil content ranging from 1.8 to 9.5%
(Table 1) with a calculated global mean of 5.8%, an oil content higher than
that of normal maize. As with maize, the oil is concentrated in the germ which
in quinoa represents 25 to 30% of the weight of the grain (Cardozo and Tapia
1979; Fuentes 1972). As the quinoa germ encircles the endosperm, we have found
that it can easily be removed by a modified polishing procedure to give a
fraction containing 19% oil.
Although special breeding programs were necessary to achieve an oil content of
6 to 8% in maize, several cultivars of quinoa already show oil contents in this
range (Table 2). Unlike maize, in which an increase in oil content resulted in
a decrease in starch content, increased oil content in the quinoa grain showed
no significant correlation with total carbohydrate content (r = 0.348) and was
negatively correlated with protein content (r = -0.910, P < 0.025) (Table 3).
Field trials were conducted with six Ecuadorian cultivars of quinoa with oil
contents between 7.2 and 8.7% (fresh weight) sown at an altitude of 3,100 m and
using experimental plots ranging in size from 0.2 to 0.5 ha (Burgasi et al.
1990). Converting the data from Table 4 to a dry matter basis gave no
significant correlation (r = 0.648) between yield and oil content, unlike maize
in which yield decreased with increasing oil content (Alexander 1989).
The potential yields of quinoa and maize oils were estimated (Table 5) for
Ecuador by multiplying the ranges of average oil content by data for average
crop yields as reported by the Ministerio de Agricultura y Ganadería
(MAG 1985). The potential yield of quinoa oil given under the general case was
calculated using the data of Nuñez and Morales (1980), who reported
quinoa yields in Bolivia of 3,960 kg/ha without fertilization and of 5,420
kg/ha with fertilization. This latter value was used to calculate a maximum
possible yield of quinoa. Nuñez and Morales (1980) extrapolated a yield
per hectare on the basis of very small experimental plots (4 rows of 6 m spaced
0.4 m apart), and their experimental plots received eight treatments against
mildew. Commercially, quinoa would likely receive one or two treatments
against mildew (M. Alvarez pers. commun.). Thus, the 488 kg oil/ha reported in
Table 5 is best cautiously interpreted as a maximum yield obtainable under
exceedingly favorable conditions.
Conversely, the exceedingly low yield of quinoa grain of 449 kg/ha reported by
MAG (1985) reflects small-scale traditional agricultural practices; hence the
calculated oil yields for Ecuador based on that data from MAG (1985) are thus
also low. Better estimates of quinoa yields in Ecuador are those given by
Burgasi et al. (1990) and reported in Table 4, which would then correspond to
potential oil yields of 102 to 306 kg/ha (Table 5). This oil yield for quinoa
compares favorably with that estimated for maize by Pryde and Doty (1981) in
the United States, namely 254 kg/ha assuming an average oil content of 4.8% for
maize.
The fatty acid composition of quinoa oil is similar to that of maize oil (Table 6). The high concentrations of linoleic and linolenic acids normally make such
oils susceptible to oxidative rancidity but both oils have relatively high
concentrations of natural antioxidants, namely tocopherol isomers. The mean
concentration of alpha-tocopherol reported for three cultivars of quinoa on
a dry weight basis was 52 ppm (De Bruin 1964), which corresponds to a
concentration of 754 ppm in the oil. Further analyses have shown quinoa oil to
contain 690 to 740 ppm alpha-tocopherol and 790 to 930 ppm
gamma-tocopherol; upon refining these concentrations fall to 450 and 230
ppm, respectively (U. Bracco pers. commun.). In comparison, refined maize oil
contains 251 ppm alpha-tocopherol and 558 ppm gamma-tocopherol (Souci et al.
1986). As optimum antioxidant activity of the alpha- and gamma-isomers
of tocopherol has been reported at 100 to 200 ppm (Hudson and Ghavami 1984)
quinoa oil would be expected to show a stability towards oxidative rancidity
similar to that of maize oil.
Quinoa can be classified according to its saponin concentrations as either
"sweet" (saponin free or having less than 0.11% saponins on a fresh weight
basis) or "bitter" (containing more than 0.11% saponins) (Koziol 1990b). The
saponins in quinoa are glycosidic triterpenoids (Burnouf-Radosevich et al.
1985; Mizui et al. 1988, 1990; Ma et al. 1989; Meyer et al. 1990; Ridout et al.
1991) and represent the major antinutritional factor found in the grain (Koziol
1992). Fortunately, most of these saponins are concentrated in the outer
layers of the grain (perianth, pericarp, seed coat, and a cuticle-like layer)
which facilitates their removal industrially by abrasive dehulling (Reichert et
al. 1986) or traditionally by washing the grains with water.
The toxicity of saponins depends upon their type, method of absorption, and
target organism (for a comprehensive review, see Price et al. 1987). Because
of their differential toxicity to various organisms saponins have been
investigated as potent natural insecticides which would have no adverse effects
on higher animals and man (Basu and Rastogi 1967). Other interest in saponins
is in their antibiotic, fungistatic, and pharmacological properties (Basu and
Rastogi 1967; Agarwal and Rastogi 1974; Chandel and Rastogi 1980; Nonaka 1986).
The pharmacological interest in saponins lies with their ability to induce
changes in intestinal permeability (Gee et al. 1989; Johnson et al. 1986)
which may aid the absorption of particular drugs (Basu and Rastogi 1967), and
with their hypocholesterolemic effects (Oakenfull and Sidhu 1990). As the
saponins in quinoa have been relatively little studied their potential
commercial uses remain unknown.
Both bitter and sweet quinoa are currently subjected to abrasive dehulling
before export from Ecuador, resulting in one case in a material concentrated in
saponins and ready for extraction and in the other a high fiber bran. A
second, modified "polishing" gives the germ fraction which can be used for oil
extraction. In preliminary trials, we found this germ fraction to contain 40%
protein. Quinoa protein is of an exceptionally high quality. Koziol (1992)
summarized the results of four different studies on the protein efficiency
ratio (PER) of quinoa in feeding trials with rats, expressing the PERs as
percentages of the casein control diets. Raw quinoa (both sweet and bitter)
exhibited PER values from 44 to 93% and cooked quinoa PER values from 102 to
105%; in comparison, raw and cooked wheat exhibited PER values from 23 to 32%
of the casein control. It is rare for a vegetable protein such as that from
quinoa to approximate so closely the quality of casein.
Comparing the profile of the essential amino acids (in human nutrition) of
quinoa with that of maize, rice, and wheat shows that quinoa protein is
particularly rich in lysine and contains more histidine and methionine +
cystine (Table 7). Of the non-essential amino acids quinoa contains more
arginine and glycine but less glutamic acid and proline than the cereals. The
protein in the quinoa oil press cake would be an important complementary
protein for improving the nutritional quality of both human and animal
foodstuffs.
The endosperm remaining after degerming the quinoa grain contains a starch with
rather unusual qualities. The majority of the starch grains are less than 3 µm
in diameter (Wolf et al. 1950; Scarpati de Briceño and Briceño
1982; Atwell et al. 1983). Small granule starches generally exhibit
gelatinization temperatures higher than those of large granule starches (Kulp
1973; Swinkels 1985) but quinoa starch initiates gelatinization at temperatures
similar to those for the larger granule wheat and potato starches, i.e. 56°
to 58°C (Scarpati de Briceño and Briceño 1982; Swinkels 1985).
Although quinoa starch initiates gelatinization at a temperature similar to
that of wheat starch, its pasting behavior is considerably different and at
equal starch concentrations shows higher viscosities than wheat starch when
measured with a Brabender amylograph (Atwell et al. 1983).
Recently, the Nutrasweet Company exploited the properties of quinoa starch and
filed a European patent for making a carbohydrate cream substitute from it
(Singer et al. 1990). Although the procedure for obtaining the starch followed
the method described by Atwell et al. (1983) for whole quinoa grains, there is
no obvious reason why degermed quinoa could not be used instead.
Quinoa offers an oil rich in polyunsaturated fatty acids, a protein whose
quality approaches that of casein and a starch that can be converted into a
cream/fat substitute, all of which are easily marketable as products or as
natural additives that should appeal to today's health conscious consumer. The
saponins removed from bitter quinoa may find niches in pharmaceutical
preparations or in programs of integrated pest management.
Despite being a promising "rediscovered" crop with important nutritional
characteristics, the current industrial use of quinoa is limited by small-scale
production which serves to keep prices for the grain too high to be
commercially competitive with wheat, rice, and barley, especially in the
Ecuadorian market. Fomenting further interest, research and the development of
improved methods of commercial cultivation both locally and worldwide (see
National Research Council 1989; Wahli 1990) will help ensure that quinoa
regains the prominence it once enjoyed under the Incas.
In Ecuador, quinoa is already adapted for cultivation at altitudes from 2,300
to 3,500 m, too high for maize yields to be commercially viable (upper limits
for maize for subsistence, not commercial, cultivation being 2,800 to 3,000 m;
yields of wheat and barley also decline notably above 3,000 m). Quinoa should
therefore be viewed as a versatile cash crop which would extend the range of
commercially arable hecterage in Ecuador.
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*Gratefully acknowledged are the efforts of U. Bracco and his research group at
the Nestlé Research Centre, Vers-chez-les-Blanc, Switzerland, for
performing the fatty acid and tocopherol analyses on samples of quinoa oil.
Table 1. Moisture and oil content of quinoa grains.
Moisture (%) | Fat (%) |
No. determinations | Mean | (Range) | No. determinations | Mean | (Range) | Reference |
3 | 10.2 | (9.8-10.5) | 3 | 6.2 | (5.5-6.7) | De Bruin (1964) |
58 | 12.7 | (6.8-20.7) | 60 | 5.0 | (1.8-9.3) | Cardozo and Tapia (1979) |
58 | 12.9 | (5.4-20.7) | 54 | 4.6 | (1.8-8.2) | Romero (1981) |
127 | 9.6 | (6.2-14.1) | 92 | 7.2 | (4.3-9.5) | Koziol (1990a) |
Table 2. High oil content cultivars of quinoa (data from Alvarez et al.
1990 for quinoa grown at Cumbayá, Ecuador).
Source | Accession | Moisture (%) | Oil (%) |
Cambridgez | Chilena-B | 8.9 | 6.7 |
| Chilena-T | 9.6 | 6.8 |
| No. 63 | 8.7 | 7.7 |
| No. 63-1 | 6.8 | 6.9 |
INIAPy | Ecu Sep 17-0271 | 11.0 | 6.9 |
| V-8 | 9.4 | 7.5 |
| V-10 | 8.7 | 7.9 |
| V-11 | 9.6 | 8.0 |
| San Juan 0036 | 7.1 | 7.8 |
Latinrecox | Potoroc | 7.2 | 7.2 |
| 011Pn | 10.1 | 7.6 |
| 011Pr | 9.7 | 7.7 |
| 012 | 7.7 | 7.8 |
| 012Pn | 8.1 | 7.8 |
| 012Pr | 10.1 | 8.7 |
| 013 | 9.4 | 7.5 |
| 013Pn | 9.7 | 8.0 |
| 013Te | 9.5 | 8.5 |
zSeed supplied by N.W. Galwey, Department of Genetics, University of
Cambridge, England.
ySeed supplied by the Ecuadorian Instituto Nacional de
Investigaciones Agropecuarias.
xEcotypes isolated by the Department of Agronomy, Latinreco, S.A.,
with the exception of 'Porotoc'.
Table 3. Composition of six genotypes of quinoa on a dry matter basis
(data from Alvarez et al. 1990 for quinoa grown at Cumbayá, Ecuador).
Genotype | Oil (%) | Protein (%) | Fiber (%) | Ash (%) | Carbohydrate (%) | Saponins (%) |
Porotoc | 7.8 | 19.0 | 3.3 | 2.6 | 67.1 | 0.2 |
V-8 | 8.3 | 18.1 | 3.1 | 3.1 | 66.4 | 1.0 |
012 | 8.5 | 19.0 | 4.2 | 3.4 | 64.7 | 0.2 |
V-10 | 8.7 | 17.6 | 3.7 | 3.6 | 65.7 | 0.7 |
013Te | 9.4 | 16.7 | 3.5 | 3.1 | 67.1 | 0.2 |
013Pr | 9.7 | 16.6 | 3.0 | 3.0 | 67.5 | 0.2 |
Table 4. Grain yield of quinoa (data from Burgasi et al. 1990; seed
moisture and fat content as per Table 2).
| Grain yield (kg/ha)z |
Accession | 1986 | 1987 | 1988 | Mean |
Porotoc | 2200 | --- | --- | 2200 |
V-8 | 1360 | --- | --- | 1360 |
012 | --- | 4500 | 3063 | 3782 |
V-10 | 2200 | --- | --- | 2200 |
013Te | 2700 | 4500 | --- | 3600 |
012Pr | 3000 | 4000 | 2956 | 3319 |
zYield data are from 0.2 to 0.5 ha experimental plots at an altitude
of 3,100 m.
Table 5. Comparison of oil yields from quinoa and maize.
| Oil yield (kg/ha) |
Source | Range of fat content (%)z | General | Ecuador |
|
Maize | 2-5y | 254x | 34-85w |
Quinoa | 2-9v | 108-488u | 9-40w |
| | | 102-306t |
zAt normal seed moisture content.
yDuke and Atchley (1986).
xPryde and Doty (1981).
wMAG (1985).
vFrom Table 1.
uCalculated on the basis of yields reported in Nuñez and
Morales (1980).
tCalculated on the basis of oil content from Table 2 and yield data
from Table 4.
Table 6. Comparison of the compositions of quinoa and maize oils.
Variable | Quinoa | Maize |
Fatty acids (as % of lipid fraction): |
Myristic | (C14:0) | 0.2z | --- | 0.2x |
Palmitic | (C16:0) | 9.9z | 11y | 11.2x |
Palmitoleic | (C16:1) | 0.1z | --- | 0.1x |
Stearic | (C18:0) | 0.8z | 0.7y | 2.1x |
Oleic | (C18:1) | 24.5z | 22y | 29.8x |
Linoleic | (C18:2) | 50.2z | 56y | 55.0x |
Linolenic | (C18:3) | 5.4z | 7y | 0.9x |
Arachidic | (C20:0) | 0.7z | --- | 0.4x |
Specific gravity | 0.891w | 0.918-0.925v |
Refractive index | 1.464w | 1.464-1.468u |
Saponification value | 190w | 189-191v |
Iodine value (Wijs) | 129w | 125-128v |
Unsaponifiable matter (%) | 5.2w | 0.8-2.9u |
Sterols (%) | 1.51w | 0.85-1.42t,s |
Lecithins (%) | 1.8w | 1-3r |
zU. Bracco (pers. commun.).
ySánchez Marroquín (1983).
xData compiled from Leibovitz and Ruckenstein (1983) and Weiss
(1983).
wDe Bruin (1964).
vMounts and Anderson (1983).
uEckey (1954).
tSouci et al. (1986).
sWeber (1983).
rPatterson (1989).
Table 7. Comparison of amino acid profiles (Koziol, 1992).
| Content (g amino acid/100 g protein) |
Amino acid | Quinoa | Maize | Rice | Wheat |
Essential (for humans): | |
Histidine | 3.2 | 2.6 | 2.1 | 2.0 |
Isoleucine | 4.4 | 4.0 | 4.1 | 4.2 |
Leucine | 6.6 | 12.5 | 8.2 | 6.8 |
Lysine | 6.1 | 2.9 | 3.8 | 2.6 |
Methionine + Cystine | 4.8 | 4.0 | 3.6 | 3.7 |
Phenylalanine + Tyrosine | 7.3 | 8.6 | 10.5 | 8.2 |
Threonine | 3.8 | 3.8 | 3.8 | 2.8 |
Tryptophan | 1.1 | 0.7 | 1.1 | 1.2 |
Valine | 4.5 | 5.0 | 6.1 | 4.4 |
Non-essential: | |
Alanine | 4.5 | 7.3 | 6.0 | 3.6 |
Arginine | 8.5 | 4.2 | 6.9 | 4.5 |
Aspartic acid | 7.8 | 6.9 | 10.0 | 5.0 |
Glutamic acid | 13.2 | 18.8 | 19.7 | 29.5 |
Glycine | 6.1 | 4.0 | 4.7 | 4.0 |
Proline | 3.3 | 9.1 | 4.9 | 10.2 |
Serine | 4.1 | 5.1 | 6.3 | 4.8 |
Last update April 17, 1997
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