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a Dep. of Agronomy, Iowa State Univ., Ames, IA 50011 USA
wfehr{at}iastate.edu
| ABSTRACT |
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Abbreviations: GLM, general linear model
| INTRODUCTION |
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380 g kg-1 (Fehr et al., 1991; J.M. Narvel, 1999, unpublished data). Soybean oil with <40 g kg-1 palmitate is more desirable than conventional soybean oil, with
110 g kg-1 palmitate, for reducing the risk of coronary heart disease (Hu et al., 1997). The development of cultivars with elevated palmitate may be desirable for producing an oil with improved oxidative stability that can be interesterified to make solid fat at room temperature that does not contain trans-fatty esters (Kok et al., 1999; Shen et al., 1997).
Elevated palmitate content up to
240 g kg-1 has been associated with changes in agronomic and seed traits. Hartmann et al. (1996) compared soybean lines with the fap2-bfap2-bfap4fap4 genotype containing
240 g kg-1 palmitate and lines with the Fap2-bFap2-bFap4Fap4 genotype containing normal palmitate of
110 g kg-1. In two populations, they observed significant negative phenotypic correlations of palmitate content with protein, oil, stearate, oleate, and linoleate contents, and a significant positive phenotypic correlation with linolenate content.
Recently, soybean genotypes with a range of palmitate contents have been developed by combining alleles developed by chemical mutagenesis. The purpose of this study was to evaluate the relationship of palmitate contents ranging from
100 to > 400 g kg-1 in these genotypes with their seed traits.
| Materials and methods |
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A five-seed bulk sample from each of five random plants in each plot was analyzed for fatty ester content with a gas chromatograph, as described by Hammond (1991). The mean of the five plants was used for data analysis. A bulk of seed from the five plants used for fatty ester analysis was evaluated for protein and oil content with a near-infrared reflectance whole grain analyzer. Protein and oil contents were adjusted to 13% moisture.
Analyses of variance were conducted with the general linear model (GLM) procedure of the SAS software (SAS Institute, 1992). Location and replication were considered random effects, and genotype was considered a fixed effect. Genotype means across locations were used for the regression of the seed traits on palmitate content with the GLM procedure and to compute the phenotypic correlation coefficients between palmitate content and the seed traits with the correlation (CORR) procedure of SAS.
| Results and discussion |
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The mean palmitate contents of 259 g kg-1 at the Agronomy Farm, 260 g kg-1 at the Burkey Farm, and 257 g kg-1 at Cedar Falls were not significantly different. The genotype x location interaction for palmitate content was not significant. The absence of a significant location effect and genotype x location interaction indicated that a limited number of environments are needed to assess the palmitate content of soybean genotypes.
Palmitate content was significantly associated with all the seed traits (Fig. 1) . The association between palmitate and protein was relatively weak, based on the small regression and phenotypic correlation coefficients for the two traits (Fig. 1a). There were genotypes with normal and elevated palmitate that had similar protein contents. It should be possible to develop cultivars with a range of elevated palmitate contents that have protein contents similar to conventional cultivars.
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250 g kg-1 had significantly lower oil contents than lines with normal palmitate. Our study indicated that oil content continued to decrease as palmitate content increased beyond 250 g kg-1 and that the genotypes with the lowest oil were among those with the highest palmitate. The decrease in oil was not offset by an increase in protein, which would have a negative impact on the value of a unit of soybean grain. For conventional soybean cultivars, the reduction in the value of a unit of grain caused by lower oil content generally is offset by an increase in value due to increased protein (Burton, 1985). For cultivars with elevated palmitate, protein would not be increased sufficiently to compensate for the reduction in oil and a premium would have to be paid for the oil to achieve grain value comparable to conventional soybean. The association between palmitate and stearate was influenced by 14 genotypes that had stearate contents >60 g kg-1 and palmitate contents >350 g kg-1 (Fig. 1c). When the genotypes were included in the regression and correlation determinations, there was a relatively strong association between palmitate and stearate (Fig. 1c). When the genotypes were excluded, the regression coefficient was reduced from 0.07 (P = 0.01) to 0.02 (P = 0.05) and the correlation coefficient was reduced from 0.58 (P = 0.01) to 0.27 (P = 0.05). Excluding those genotypes, there were lines with elevated palmitate that had normal stearate contents. It should be possible to develop soybean cultivars with elevated palmitate that have normal or elevated stearate content.
There was a strong negative association of palmitate content with oleate and linoleate contents (Fig. 1d and 1e). None of the genotypes with elevated palmitate had oleate or linoleate contents similar to those of genotypes with normal palmitate. Hartmann et al. (1996) observed similar strong negative associations of elevated palmitate with reduced oleate and linoleate. Cultivars with elevated palmitate would be expected to have reduced contents of the two fatty esters.
Palmitate and linolenate contents were positively associated (Fig. 1f). The same positive association was reported by Hartmann et al. (1996) and Bravo et al. (1999) for genotypes with
250 g kg-1 palmitate. The increase in linolenate was not expected because of the reduction in oleate and linoleate that was observed with increased palmitate. Our study supports the conclusion of Hartmann et al. (1996) that the development of cultivars with elevated palmitate and normal linolenate would be difficult, unless genes for reduced linolenate were included in the breeding program. Bravo et al. (1999) combined the fan1(A5) and fan2 alleles for reduced linolenate with the fap2-b and fap4 alleles for elevated palmitate and obtained lines with >250 g kg-1 palmitate and <50 g kg-1 linolenate. They did not recover any lines that had linolenate content <30 g kg-1, as has been obtained when the alleles for reduced linolenate were in a genotype with the Fap2 and Fap4 alleles for normal palmitate. The unexpected result emphasized that it is not always possible to predict the way in which soybean oil composition will be changed by combining major genes for altered fatty esters.
With the available genotypes, it was not possible to evaluate the relationship of elevated palmitate with agronomic traits. Research is in progress to determine the agronomic performance of genotypes with >400 g kg-1 palmitate. It also would be appropriate to evaluate oil with >400 g kg-1 palmitate for oxidative stability in frying applications and for producing plastic fats without hydrogenation (Shen et al., 1997; Kok et al., 1999).
| NOTES |
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Received for publication May 17, 1999.
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