Abstract
Lipoxygenase-2 present in soybean seeds is the prime contributor to off-flavour generated during the processing of soy products. Genetic elimination of this undesirable component is important as the heat inactivation not only incurs extra cost but also affects the protein solubility. The present study was aimed at eliminating lipoxygenase-2 from cultivar ‘JS97-52’ through marker assisted introgression of null allele of Lox2 from PI596540 (lox2lox2). Foreground selection in BC1F1, BC2F1 and BC3F1 of the cross ‘JS97-52’ × PI596540 was carried out using lox2 specific marker, while lox2 specific marker in combination with SSR marker Satt656 tightly linked with Lox2 locus was employed for identification of homozygous recessive plants (lox2lox2) in BC2F2 and BC3F2. Background selection performed using 150 polymorphic markers resulted in development of 12 Lox2-free soybean lines (BC3F2:3 seeds) exhibiting recurrent parent genome content in the range of 97.66-98.66%. Qualitative and quantitative assays confirmed the absence of Lox2 in introgressed lines (ILs). The ILs were at par in days-to-flowering, days-to-maturity,100-seeds weight, yield and protein content with the recurrent parent but showed significant improvement in seed longevity over the latter.
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Key words: Lipoxygenase-2, Marker assisted backcrossing, Soybean, Seed longevity
INTRODUCTION
Soybean being one of the most economical source of protein can mitigate mal- and under-nutrition in developing countries. It ideally fits in the dietary regimes of people who seek nutritious but follow vegetarian/vegan diet. Moreover, plethora of studies revealed the protective effects of soybean several bioactive compounds like isoflavones, Bowman-Birk factor, tocopherols, lecithin, lunasin, saponins etc., against cancer, atherosclerosis, diabetes, osteoporosis etc. (
Kumar et al. 2010;
Messina 2016). These health-promoting attributes of soybean have earned this crop the ‘function food’ status. However, soy products have not been able to permeate into daily diet of masses across the world as indicated by the fact that barely 10% of the total global production of soybean is utilized in food uses, most of it confined to East and South East Asia where soy products are in the staple diet since centuries ago. Besides the presence of antinutritional factor Kunitz trypsin inhibitor and allergens, such as a subunit of b-conglycinin (Gly m Bd 68K) and P34 glycoprotein (Gly m Bd 30K) in soybean which deters the utilization of soybean for human consumption, beany flavour associated with soy products is also responsible for the aversion of people to the inclusion of this bean in the daily diet in several countries including India. The biochemical basis of the generation of this off-flavour is the catalytic oxidation of 1,4-Z,Z-pentadiene-containing polyunsaturated fatty acids
viz. linoleic and a linolenic acid by seed lipoxygenases. The hydroperoxides so formed are further metabolized by hydroperoxide lyases, thereby generating volatile aldehyde and ketone compounds, which impart characteristic off/beany flavour to the soy products (
Baysal and Demirdoven 2007).
Soybean seed lipoxygenase exists in three forms
viz. lipoxygenase-1, lipoxygenase-2 and lipoxygenase-3 which differ in their substrate specificity, pH optima and electrophoretic mobility. Null forms of these three seed lipoxygenases are controlled by single recessive
loci, designated as
lox1,
lox2 and
lox3 (
Kitamura et al. 1983;
Davies and Nielsen 1986). Heat inactivation of lipoxygenases at industrial level is not only cost-ineffective but also affects functionality of proteins (
Macleod and Ames 1988). Therefore, genetic elimination of lipoxygenase-2 is the key to spur utilization of soybean in food uses. Of the three lipoxygenases, lipoxygenase-2 is mainly responsible for the generation of n-hexanal (
Nishiba et al. 1995;
Mellor et al. 2010). Genetic removal of lipoxygenase-2 has been reported to improve the flavor of soy products considerably (
Davies et al. 1987;
Wilson 1996). Soymilk and
tofu prepared from IA2011, a commercially available Lox2-free soybean variety developed by Iowa State, have been demonstrated to be devoid of beany flavour (
Shurtleff and Aoyagi 2014). Soybean genotypes, namely, PI086023, PI596540 for null allele for lipoxygenase-2 have been reported (
Davies and Nielsen 1986;
Pfeiffer et al. 1997). These accessions were procured by ICAR-National Bureau of Plant Genetic Resources, New Delhi, India and delivered to ICAR-Indian Institute of Soybean Research, India for developing lipoxygenase-2 free soybean which would give reduced off-flavour under the plant breeding programme focusing on development of food-grade soybean. Using PI086023 as the donor parent for lipoxygenase-2, first lipoxygenase-2 free soybean NRC109 was developed in India by crossing it with early maturing Indian soybean genotype ‘Samrat’ (
Kumar et al. 2013). Subsequently, it was thought worthwhile to introgress null allele of lipoxygenase-2 (
Lox2) into high yielding soybean varieties through Marker assisted backcrossing (MABC). This plant breeding approach comprising of foreground and background selection is an expeditious process over conventional backcross breeding to transfer a trait in the desirable genetic background, and has been employed for introgression of useful traits in soybean (
Zhu et al. 2007;
Kim et al. 2008;
Kumar et al. 2015).
Lox2 locus has been mapped on LG ‘F’, and SSR markers tightly linked to
Lox2 locus were identified (
Kim et al. 2004;
Kumar et al. 2014) and SSR marker specific to null allele of
Lox2 were designed (
Reinprecht et al. 2011;
Shin et al. 2012). This facilitated and expedited the foreground selection of the individual plants carrying null allele (
Lox2
lox2/
lox2
lox2) in plant population segregating for lipoxygenase-2. In the presented work, we employed MABC approach for introgression of null allele of lipoxygenase-2 (
lox2) from germplasm accession PI596540 into a high yielding Indian soybean variety ‘JS97-52.’ For this purpose, sufficient number of polymorphic markers (
loci) between the genetically diverse donor (PI596540) and recipient (‘JS97-52’) parents reported previously (
Rawal et al. 2014) were employed to recover the gene pool from the recurrent parent.
MATERIALS AND METHODS
Parent materials
Recipient genotype
Soybean variety ‘JS97-52’ is a high yielding variety released for cultivation in Central India. Though, this variety is lipoxygenase-2 positive like other varieties released for cultivation under All India Co-ordinated Research Project, but it gives excellent field emergence and shows resistance against multiple diseases, such as yellow mosaic virus disease, root rot, bacterial pustule, charcoal rot, cercospora leaf spot and target leaf spot. Further, the variety is tolerant to water-logging conditions, which the crop has to face in the event of heavy precipitation in a very short period during the monsoon season. The genotype flowers in 47-50 days and attains maturity in 105 days in the agroclimatic conditions of Central India.
Donor genotype
PI596540, lacking lipoxygenase-2 activity (
lox2
lox2 genotype), was procured from United State Department of Agriculture was used as a donor. This genotype is derived from Camp × (‘Vance’
2 × L
2-3) and was developed at Kentucky Agricultural Experimental Station (
Pfeiffer et al. 1997). In agroclimatic conditions of Central India, this genotype flowers in 27-29 days and reaches harvest maturity in 85 days.
To identify the individual plants harbouring the target allele in first filial generations in the backcross progenies BC
1F
1, BC
2F
1 and BC
3F
1, null allele of
Lox2 (
lox2) specific primer given by
Reinprecht et al. (2011) was employed. SSR marker Satt656 which was identified to be tightly linked with
Lox2 locus (
Kumar et al. 2014) was used in conjunction with null allele specific marker for the identification of homozygous recessive plants (
lox2
lox2) in BC
2F
2 and BC
3F
2 generations. Oligonucleotide sequences of null allele (
lox2) specific marker and linked marker Satt656 are given in
Table 1. For the background selection, 150 polymorphic SSR markers between ‘JS97-52’ and PI596540 were used, some of them have been reported earlier (
Rawal et al. 2014). SSR markers were selected from 20 LGs of soybean molecular linkage map as given by United State Department of Agriculture (bldg6.arsusda. gov/cregan/soymap.html). The synthesis of the molecular markers was outsourced to Sigma Aldrich, Bangalore.
Genomic DNA was extracted from young leaves of the two parental genotypes F1s and backcross progenies following CTAB (Cetyl trimethyl ammonium bromide) procedure. DNA was purified and its concentration was quantified using spectrophotometer (Model UV 1601, Shimadzu) and final concentration was adjusted to ∼25 ng/mL. Polymerase Chain Reaction (PCR) was carried out for amplification of the genomic DNA using linked (Satt656) and polymorphic SSR markers, in 10 mL reaction mixture containing 2 mL DNA (25 ng/mL), 1 mL PCR 10x buffer, 1.1 mL MgCl2 (25 mM), 0.1 mL dNTPs (25 mM), 0.4 mL each forward and reverse SSR primers (30 ng/mL), 0.068 mL Taq DNA polymerase (3 U/mL) and 4.932 mL distilled water. DNA was denatured in the thermocycler (Lifepro Bioer) at 94℃ for 2 minutes, followed by 30 cycles each consisting of denaturation at 94℃ for 1 minute, primer annealing at 50℃ for 2 minutes, primer elongation at 72℃ for 3 minutes and final elongation at 72℃ for 10 minutes, using linked and polymorphic SSR markers. PCR conditions for amplification through null allele specific marker were: initial denaturation at 94℃ for 2 minutes followed by 35 cycles each consisting of denaturation at 94℃ for 30 seconds, primer annealing at 58.4℃ (lox2 specific) for 45 seconds, primer elongation at 72℃ for 1 minute and final elongation at 72℃ for 10 minutes. Amplified products from gene specific marker were resolved on 1% agarose, while PCR amplified products through SSR marker Satt656 and all other SSR markers were resolved using 8% polyacrylamide gel (PAGE) and 3% metaphor agarose, respectively. The images were analyzed in Gel documentation unit (Syngene).
Backcrossing
Due to the difference of about 20 days in days-to-50% flowering of the donor and the recipient parent, staggered sowing of ‘JS97-52’ and PI596540 was done to synchronise the buds of ‘JS97-52’ with the flowering stage of PI596540. Crosses were effected between the parent plants by transferring the pollens from PI596540 to the stigma of JS97-52 to generate F1 seeds. True F1 plants confirmed using polymorphic SSR marker Satt522 (LG ‘F’) were subjected to first backcrossing using ‘JS97-52’ as a female parent. Foreground-selected BC1F1 individuals were subjected to background selection and the individuals carrying maximum recurrent parent genome (RPG) were used as male parent for effecting BC2F1 generation. BC2F1 individuals with the target allele and with highest % RPG content were selfed. Foreground-selected BC2F2 homozygous recessive individuals (lox2lox2) were used to pollinate ‘JS97-52’ to advance to BC3F1 generation. True BC3F1 individuals carrying lox2 allele were selfed to obtain BC3F2 generation.
Assessment of recurrent parent genome content
For assessing the RPGC for an individual plant surveyed through a set of SSR markers (loci), score ‘1’ was given to heterozygous locus (H), while the locus homozygous for recurrent parent (A) was given a score of ‘2’. SSR markers exhibiting homozygosity for the donor parent (B) were given ‘0’ score. Percent RPGC was computed by summing up the score of an individual plant given for all the loci divided by total number of alleles (2 × number of SSR markers surveyed).
Phenotyping
Qualitative determination of Lox2 isozyme
Soybean flour of ‘JS97-52’, PI596540 and ILs was subjected to dye bleaching assay as given by Suda et al. (1995). To ascertain the phenotype, minimum 5 individual seeds from each plant were analysed. For this purpose soybean flour (5 mg) from each seed was weighed into a test tube and 0.5 mL of distilled water was added. The mixture was stirred lightly and allowed to stand for 1-10 minutes. Dye-substrate solution was prepared for 20 samples by mixing 154.25 mg of dithiothreitol, 25 mL of 200 mM sodium phosphate buffer (pH 6.0), 5 mL of 100 mM methylene blue dye, 5 mL of 10 mM sodium linoleate substrate and 5 mL of acetone in a 100 mL glass stoppered bottle. In the test tube containing sample, 2 mL of the dye-substrate solution was added and the change in blue colour of the solution was observed.
Quantitative estimation of Lox2 isozyme activity
Quantitative estimation of MABC-derived Lox2-null ILs was carried out through enzymatic assay for the absence of lipoxygenase-2 isozyme. Crude extract was prepared by homogenisation of 0.5 g of the defatted soy flour with 50 mL of sodium phosphate buffer (0.2 M, pH 6.8) in a microtissue polytron homogenizer at 20,000 rpm for 20 minutes at 0-4℃. The homogenised solution was centrifuged at 10,000 rpm for 10 minutes at 4℃. The supernatant so obtained was used as crude extract for the enzymatic assay following the method given by
Axelrod et al. (1981). Reaction mixture consisted of 2.8 mL sodium phosphate buffer (0.2 M, pH 6.1), suitable volumes of crude extract and 10 mM sodium arachidonate as a substrate. The change in absorbance was recorded in spectrophotometer (Model UV1601, Shimadzu) at 238 nm after every 15 seconds. One unit of enzyme was taken as equivalent to the amount of enzyme that generated an increase in absorbance of 1.0 per minute at 238 nm.
For this purpose, seeds were sown in single row plot of 3 m length maintaining plant-to-plant and row-to-row distance of 5 and 45 cm, respectively, in random block design. The dates of 50% percent flowering and the harvest maturity of each genotype in each replicate were recorded. Yield of each genotype in each replicate was recorded and expressed in Kg/hac. Randomly drawn 100 seeds from the harvest of from each replicate were weighed to determine 100 seeds weight. For assessing the seed longevity, the seeds were stored at ambient temperature in polythene bags for a period of two years. Two hundred seeds of each genotype were drawn in 3 replicates immediately after the harvest, and test for germination percentage immediately, and after a period of 12 and 24 months. For this purpose, soybean seeds were placed on sterile damp germination paper and incubated at 28°C for 4 days in a seed germinator. Germination percentage was calculated as follow: Total number of germinated seeds divided by total number of seeds tested multiplied by 100.
Statistical analysis
All statistical analyses were carried out using SAS 9.3.
RESULTS
One hundred fifty polymorphic SSR markers (their respective LGp/chr and the position (cM) on the LGp/chr is given in
Table 2) were found for the parental combination JS97-52 × PI596540. For the introgression of null allele of
Lox2 into ‘JS97-52’ from PI596540 (donor of
lox2 allele), crosses were effected between ‘JS97-52’ (female) and PI596540 (male).
Table 3 details about the foreground and background selection at various stages of backcross generation. Screening of F
1 generation using polymorphic SSR marker Satt522 led to identification of 12 true F
1 plants.
First Backcross generation
True F
1 plants were used as male parents to pollinate recurrent parent ‘JS97-52’ to effect BC
1F
1 generation. BC
1F
1 individuals (165 plants) grown in the field were subjected to foreground selection using null allele specific marker given by
Reinprecht et al. (2011) (
Fig. 1a). This led to the identification of 59 true BC
1F
1 individuals (
Lox2
lox2). Of these, 24 plants exhibiting morphological similarity with the recipient parent
i.e. ‘JS97-52’, were selected for first background selection using 150 polymorphic SSR markers (
Table 2) for ‘JS97-52’ and PI596540, across the genome. This revealed recurrent parent genome content to the range of 72-83%.
Second Backcross generation
To further minimise the genomic segments from the donor parent, 5 BC
1F
1 individuals exhibiting RPGC in the range of 80-83% were used as male parent to pollinate recurrent parent ‘JS97-52’. Foreground selection of BC
2F
1 individuals (127) with null allele specific marker resulted in the confirmation of 54 true BC
2F
1 plants (
Lox2
lox2) carrying null allele of
Lox2 (
Table 3). Among these, 16 plants were morphologically similar to recurrent parent. Nine out of these 16 BC
2F
1 individuals which showed recombination with flanking marker Satt522 (located on the other side of
Lox2 locus with respect to the position of Satt656) were subjected to background selection using 51-60 SSR markers, which were heterozygous in the previous backcross generation (BC
1F
1). This revealed retrieval of 84-94.33% of recurrent parent genome in the selected BC
2F
1 individuals. However, 5 plants exhibiting RPGC between 91.33-94.33% were selfed. BC
2F
2 generation (1109) was raised and screened with null allele specific marker for identification of plants carrying null allele of lipoxygenase-2. However, application of null allele specific marker did not distinguish
Lox2
lox2 from
lox2
lox2 plant individuals. Therefore, the plants found to carry null allele of
Lox2 were, subsequently, surveyed with tightly linked marker Satt656 (flanking
Lox2 locus), which led to the identification of 250 homozygous recessive (
lox2
lox2) plants. Of these, 35 plants similar to recurrent parent in morphology when subjected to background selection (III
rd) using 17-26 polymorphic SSR markers, which were heterozygous in the BC
2F
1 generation, revealed a range of 89.33-96.66% RPGC.
Third Backcross generation
To enhance the recovery of recurrent parent (‘JS97-52’) genome, pollens from 8 BC
2F
2 plants exhibiting more than 94.33% RPGC were used to effect BC
3F
1 generation. Foreground selection of BC
3F
1 plants using gene specific marker resulted in identification of 31 true BC
3F
1 plants carrying
lox2 allele (
Lox2
lox2), which were subjected to background selection at 8-13
loci, which were either heterozygous or both the alleles were from the donor parent genome in the previous background selection (BC
2F
2 generation). Five plants which exhibited 98% retrieval of recurrent parent genome were selfed. BC
3F
2 generation was raised and subjected to foreground selection first using null allele specific marker (
Fig. 1b). The plants identified to harbour null allele of
Lox2 (
Lox2
lox2/
lox2
lox2) were subsequently surveyed using tightly linked marker Satt656 (
Fig. 1c). This resulted in the identification of 260 homozygous recessive plants (
lox2
lox2), all of which were surveyed using 6 SSR markers, heterozygous in the previous background selection (BC
3F
1). This showed a recovery of 96.33-98.66% of recurrent parent genome. However, 12 lines (BC
3F
2:3) exhibiting recurrent parent genome recovery of 97.66-98.66% were selected as the ILs for confirmation of absence of lipoxygenase-2 through dye bleaching and quantitative test.
For analysing the recovery of recurrent parent genome in ILs on the chromosome carrying
Lox2 locus, 10 polymorphic SSR markers (Satt193, Sat_240, Satt516, Satt595, Sat_234, Sct_033, Sct_188, Satt144, AW756935 and Satt395) other than Satt656 and Satt522 (used for foreground selection) on the LGp F (
chr 13) were surveyed (
Fig. 2). SSR markers Sat_240, Satt516, Satt595, Sat_234 and Satt395 were fixed for the recurrent parent genome in all the 12 ILs. However, Satt193, Sct_033, Sct_188 and Satt144 were not fixed for the recurrent parent in all the ILs, as some of the ILs exhibited either heterozygosity or were found to carry both the alleles from the donor parent (PI596540) at one or more of these
loci. Further, in BC
3F
2 generation an SSR marker AW756935 (124.9 cM) which has been mapped between flanking SSR markers
viz. Satt522 (119.2 cM) and Satt656 (135.1 cM) (USDA 2008), was also found to be fixed for the recurrent parent allele in one IL, namely, P111-27-9-3-7. However, 4 ILs exhibited heterozygosity at locus AW756935, and remaining 7 ILs exhibited donor parent alleles in homozygous state. Therefore, line P111-27-9-3-7 exhibited minimum introgression of donor parent genome on the carrier chromosome.
Results of dye-bleaching test performed using the soy flour from parent genotypes
viz. ‘JS97-52’, PI596540 and 12 ILs are presented in
Table 4. Dye-substrate (methylene blue-sodium linoleate) solution containing soy flour from the recurrent parent (‘JS97-52’) exhibited bleaching of dye within 1 minute. On the contrary, soy flour of PI596540 and ILs did not cause fading of the dye even after 7 minutes. Stability of dye-color in MABC-derived Lox2-free ILs confirmed the absence of lipoxygenase-2 isozyme. Lipoxygenase-2 activity per gram of defatted soy flour in the recipient parent ‘JS97-52’ (
Lox2
Lox2) and donor parent PI596540 (
lox2
lox2) was 450.21 and, 40 units per gram of defatted flour, respectively, while 12 ILs exhibited negligible activity of 35.24-46.21 units/g of defatted flour, which was at par with the donor parent PI596540 (
Table 4). Qualitative data of parents and ILs corresponded well with the results of quantitative assay, which confirmed the absence of lipoxygenase-2 in ILs. Further, the protein content in most of the ILs was at par with the recurrent parent ‘JS97-52’. Results presented in
Table 4 also showed that the germination percentage of the recurrent parent was at par with the ILs immediately after the harvest. After storage at ambient temperature for 12 months, recurrent parent registered 71% germination, which plummeted to 30.3% after 24 months. On the contrary, % germination among 12 ILs was 82.0-90.0% and 49.0-55.2% after 12 and 24 months of storage.
DISCUSSION
Despite being increasingly recognized as the economical source of protein to address under-nutrition in developing countries and as ‘functional food’ to stave off broad spectrum of diseases across the world, utilization of soybean in food uses stands minuscule. Off-flavour associated with the soy products deter masses to incorporate of soybean in daily diet in several countries including India. The off-flavour is ascribed to the aldehyde and ketone compounds released during the oxidation of polyunsaturated fatty acids by the lipoxygenases present in the seed. Of the three lipoxygenases, lipoxygenase-2 is the prime contributor to off-flavor as the isozyme generates maximum n-hexanal-producing 13-hydroperoxides (
Mellor et al. 2010). Genetic elimination of lipoxygenase-2 is critical for the flavour improvement of soy products (
Davies et al. 1987). Like the other two isozymes, expression for
Lox2 is also governed by single dominant gene and the sources of recessive form have also been identified (
Kitamura et al. 1983;
Davies and Nielsen 1986). Two flanking SSR markers, namely, Satt522 and Satt656 around
Lox2 locus, have been identified to be linked to
Lox2 at a distance of 9.3 and 2.7 cM on LG ‘F’ (
chr 13) in the mapping population derived from ‘JS97-52’ × PI596540 in the previous study (
Kumar et al. 2014). Further, null allele specific marker for
lox2 has been developed by
Reinprecht et al. (2011). Since the parentage of donor genotype PI596540 used in the present work is Camp x (‘Vance’
2 × L
2-3), and the L
2-3 is the progeny of PI086023, we could successfully amplify the genomic DNA of the null plants (
lox2
lox2) using null allele specific marker given by
Reinprecht et al. (2011) and deployed it in carrying out foreground selection in BC
1F
1, BC
2F
1 and BC
3F
1 generation. In BC
2F
2 and BC
3F
2 generation, null allele specific marker in conjunction with linked SSR marker Satt656 enabled the identification of homozygous recessive plants (
lox2
lox2). The high level of SSR polymorphism (49.24%) detected between the genome of ‘JS97-52’ and PI596540 in our previous report (
Rawal et al. 2014) was exploited for faster recovery of the recurrent parent genome using marker assisted background selection.
First background selection in 24 individuals morphologically similar to ‘JS97-52’ in first backcross generation using 150 polymorphic SSR markers identified across 20 LGs exhibited RPGC in the range of 72-83% against the expected average recovery (75%).
Kim et al. (2008) employed 26 and 21 SSR markers in the first background selection, with the objective of introgressing
rxp locus responsible for imparting bacterial leaf pustule resistance into 2 soybean varieties ‘Hwangkeumkong’ and ‘Taekwangkong’ and reported 76.9-96.1 and 61.9-95.2% recurrent parent recovery, respectively. Higher RPGC recovery in the first background selection in both the varieties compared to our results may be ascribed to relatively lesser number of SSR markers employed by
Kim et al. (2008). We conducted second background selection in the BC
2F
1 generation using 51-60 SSR markers, as the remaining SSR markers were fixed for the recurrent parent. This led to the recovery of 84-94.33% RPGC with some of the plants showing RPGC, exceeding the expected recovery of 87.5% at this stage. In a marker assisted backcross breeding program in maize focusing on development of low phytic acid genotype, retrieval of RPGC to the magnitude of 92.15% in BC
2F
1 generation has been reported (
Naidoo et al. 2012).
Kim et al. (2008) reported background recovery of 82.2-91.5 and 85.5-93.3% during the introgression of
rxp locus responsible for imparting bacterial leaf pustule resistance in varieties ‘Hwangkeumkong’ and ‘Taekwangkong’. The range of recovery of RPGC in this study is in proximity with our observation in BC
2F
1 generation. Third background selection carried out in BC
2F
2 (
lox2
lox2) progenies using 17-26 loci, which remained in heterozygous condition in BC
2F
1 generation, revealed RPGC higher/lower compared to their corresponding BC
2F
1 parent. Lower recurrent parent genome recovery in some of BC
2F
2 (homozygous recessive for
lox2 allele) progenies is due to fixation of heterozygous alleles towards donor parent genome while higher % RPGC compared to their corresponding BC
2F
1 parent is attributed to the realization of homozygosity for recurrent parent at several heterozygous loci. As we did not observe recurrent parent genome content recovery more than 96.66% in BC
2F
2 generation; therefore, third backcross generation was effected to enhance the RPGC recovery. Background selection in BC
3F
1 generation using 8-13 SSR markers, which were heterozygous or fixed towards donor parent genome in BC
2F
2 generation, resulted in identification of plants with 96.66-98% RPGC. The last background selection performed in BC
3F
2 homozygous recessive (
lox2
lox2) individuals using remaining heterozygous loci (6) led to identification of 12 BC
3F
2 lines with 97.66-98.66% RPGC.
In the presented work, PI596540 as the donor parent of null allele of
Lox2 exhibited short-stature and poor yield. Therefore, development of Lox2-null ILs with minimum linkage drag was sought. Satt656 and Satt522 are two flanking markers around
Lox2 locus at 2.7 and 9.3 cM, respectively (
Kumar et al. 2014). The former SSR marker was employed for foreground selection, while plants exhibiting recombination with Satt522 in BC
2F
1 generation were carried to BC
3 generation to minimize the linkage drag in the ILs. One IL (P111-27-9-3-7), which showed recovery of SSR marker AW756935 (124.9 cM) mapped between flanking SSR markers
viz. Satt522 (119.2 cM) and Satt656 (135.1 cM), carried minimum donor parent genomic content, except the region governing the expression of trait.
The data pertaining to the biochemical and agronomic characters of ILs and both the parents are presented in
Table 4. Soy flour from ILs (BC
3F
2:3) did not cause bleaching of the dye colour in qualitative assay. Quantitative estimation of lipoxygenase-2 showed negligible activity of lipoxygenase-2 at par with the donor parent PI596540 (
Table 4). Negligible activity of lipoxygenase-2 observed in donor parent PI596540 and ILs may be ascribed to the presence of other lipoxygenase-like enzymes as discussed by
Iassonova et al. (2009) or any other metabolic pathway involved in the generation of n-hexanal (
Mellor et al. 2010). All the JS97-52-derived lipoxygenase-2 free ILs were at par with the recurrent parent in days-to-50% flowering (47-50 days), days-to-maturity (102-107 days), and yield (2572-2686 kg/ha). Both the donor and the recurrent parent were small seeded, and the null Lox-2 ILs exhibited the same 100 seed weight as that of the recurrent parent. However, seed longevity of ILs was better than recurrent parent as indicated by the higher germination percentage of the former than the latter after 12 and 24 months of storage at ambient temperature. Suppressed lipoxygenase activity has also been reported to enhance seed longevity during storage in other crops such as tobacco (
Li et al. 2018), rice (
Ma et al. 2015). This may be attributed to the reduction in lipid peroxidation of cell membrane due to lower levels of lipoxygenase-produced reactive oxygen species.
In the presented work, introgression of null allele of Lox2 into a high yielding soybean cultivar ‘JS97-52’ by deploying marker assisted foreground and background selection was expeditiously accomplished. Null Lox2 introgressed lines showed same biochemical and morpho-physical traits as that of the recurrent parent except the improved seed longevity of the former over the latter. Use of these Lox2-free lines as initial raw material in soy processing industries would deliver soy-based products with reduced off-flavour and the seeds of these breeding lines can be stored for longer period under ambient conditions. More importantly, these ILs can also be used for pyramiding Lox2-null with null forms of other two lipoxygenase isozymes viz. lipoxygenase-1 and lipoxygenase-3 for development of triple null-lipoxygenase soybean.
Notes
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CONFLICT OF INTEREST
The authors declare that they have no conflict of interest.
Fig. 1Foreground selection in BC1F1 (a) and BC3F2 (b) generations using null allele specific marker on 1% agarose gel and in BC3F2 (c) generation using linked marker Satt656 on 8% polyacrylamide gel.
Fig. 2Graphical genotyping of selected plants in BC1F1 (a), BC2F1 (b), BC2F2 (c), BC3F1 (d) and BC3F2 (e) generations on carrier chromosome (LG ‘F’ i.e. chr 13) through GGT 2.0 (Berloo 2008).
Table 1Oligonucleotide sequences of Lox2 linked and null allele specific molecular marker along with their corresponding annealing temperature.
Table 1
|
Marker |
Primer sequences |
Annealing temperature (℃) |
|
Satt656 |
F-5ʹGCGTACTAAAAATGGCAATTATTTGTTG-3ʹ |
50.0 |
|
R-5ʹGCGTGTTTCAGTATTTGGATAATAGAAT-3ʹ |
|
lox2 specific (Reinprecht et al. 2011) |
F 5ʹ-GTTCATAGGTTAAATACTCAA-3ʹ |
58.4 |
|
R 5ʹ-TTTCAACAAGCTCTTCAAT-3ʹ |
Table 2Details of 150 SSR markers, spanning soybean genome, deployed for backcross selection.
Table 2
|
LGp (Chr) |
NO of SSR markers |
SSR markers with position (cM) on the LGp (chr) |
|
LGpA1 (chr5) |
9 |
Sat_137 (0.00 cM), Satt684 (3.54 cM), Satt368 (14.37 cM), Satt276 (17.16 cM), Satt042 (27.66 cM), Satt717 (51.95 cM), Sat_171 (57.79 cM), Satt545 (71.39 cM), Satt211 (95.68 cM) |
|
LGpA2 (chr8) |
10 |
Satt589 (33.96 cM), GMENOD2B (58.44 cM), AW132402 (67.86 cM), Satt341 (77.70 cM), Satt089 (87.57 cM), Satt233 (100.09 cM), Satt329 (110.94 cM), Satt421 (115.93 cM), Sat_294 (131.97 cM), Satt228 (154.11 cM) |
|
LGPB1 (chr11) |
10 |
BE806308 (0.00 cM), Satt509 (32.51 cM), Satt638 (37.80 cM), Satt197 (46.39 cM), Sat_128 (53.41 cM), Satt597 (73.77 cM), Sct_026 (78.13 cM), Satt444 (85.92 cM), Satt665 (96.36 cM), Sat_331 (125.74 cM) |
|
LGpB2 (chr14) |
8 |
Satt577 (6.05 cM), Sat_342 (20.31 cM), Sat_287 (31.88 cM), Sat_355 (66.24 cM), Satt556 (73.21 cM), Sat_009 (78.66 cM), Satt560 (97.92 cM), Satt687 (113.61 cM) |
|
LGpC1 (chr4) |
5 |
Sat_337 (32.10 cM), Satt607 (67.03 cM), Satt646 (70.52 cM), Sat_085 (76.91 cM), Sat_042 (82.51 cM) |
|
LGpC2 (chr6) |
6 |
Satt681 (3.15 cM), Satt281(40.3 cM), Sat_213 (90.93 cM), Satt277 (107.59 cM), Sat_312 (112.85 cM), Satt371 (145.48 cM) |
|
LGpD1a (chr1) |
7 |
Sat_332 (5.25 cM), Satt320 (46.8 cM), Satt267 (57.34 cM), Satt580 (62.37 cM), Satt468 (69.91 cM), Satt077 (77.49 cM), Satt129 (109.67 cM) |
|
LGpD1b (chr2) |
10 |
Sat_096 (0 cM), Sat_279 (3.79 cM), Satt095 (25.6 cM), Satt266 (59.61 cM), Satt005 (75.29 cM), Satt041 (84.04 cM), Sat_183 (112.63 cM), Sat_202 (118.86 cM), Staga002 (126.45 cM), Sat_192 (135.26 cM) |
|
LGpD2 (chr17) |
4 |
Sct_192 (11.77 cM), Sat_292 (75.29 cM), Satt311(84.62 cM), GMHSP179 (99.04 cM) |
|
LGpE (chr15) |
5 |
Sat_124 (15.86 cM), Satt651 (32.1 cM), Sat_172 (42.74 cM), Satt369 (56.27 cM), Satt553 (67.92 cM) |
|
LGp F (chr13) |
10 |
Satt193 (3.42 cM), Sat_240 (25.58 cM), Satt516 (44.42 cM), Satt595 (50.24 cM), Sat_234 (66.55 cM), Sct_033 (74.13 cM), Sct_188 (85.30 cM), Satt144 (102.08 cM), AW756935 (124.88 cM), Satt395 (146.42 cM) |
|
LGp G (chr18) |
10 |
Satt163 (0.00 cM), Sat_163 (10.06 cM), Satt217 (18.25 cM), Sat_315 (27.48 cM), Satt324 (33.26 cM), Satt115 (43.78 cM), Satt303 (53.42 cM), Satt400 (63.28 cM), Satt472 (94.84 cM), Sat_372 (107.75 cM) |
|
LGp H (chr12) |
9 |
(27.64 cM), Satt009 (38.89 cM), Satt442 (46.95 cM), Satt541 (53.35 cM), Sat_205 (68.18 cM), Sat_158 (73.46 cM), Satt637 (85.79 cM), Satt181 (91.12 cM), Sat_180 (104.37 cM) |
|
LGpI (chr20) |
4 |
Satt562 (22.84 cM), Satt354 (46.22 cM), Satt650 (63.33 cM), Sat_170 (75.00 cM) |
|
LGpJ (chr16) |
8 |
AW310961 (5.19 cM), Satt674 (15.95 cM), Sat_339 (27.97 cM), Satt280 (38.7 cM), Satt380 (43.01 cM) Sctt011 (62.89 cM), Sat_224 (75.13 cM), Sat_393 (90.33 cM) |
|
LGpK (chr 9) |
7 |
Satt539 (1.8 cM), Sat_119 (17.11 cM), Satt349 (42.39 cM), Satt710 (51.00 cM), Sat_043 (61.67 cM) Sat_126 (108.2 cM), Satt588 (117.02 cM) |
|
LGpL (chr19) |
7 |
Sat_301(11.12 cM), Satt523 (27.92 cM), Satt278 (31.22 cM), Sat_150 (53.67 cM), Satt229 (93.89 cM), Satt513 (106.37 cM),Sat_245 (115.07 cM) |
|
LGpM (chr7) |
8 |
Satt435 (38.94 cM), Sat_244 (48.86 cM), Satt626 (58.60 cM), Satt175 (66.99 cM), Sat_288 (76.41 cM), Satt551 (95.45 cM), Satt308 (130.76 cM), Sat_330 (140.69 cM) |
|
LGpN (chr3) |
6 |
Satt641 (29.28 cM), Sat_084 (36.86 cM), Satt080 (45.14 cM), GMABAB (73.1 cM), Sat_295 (95.00 cM), Satt022 (102.06 cM) |
|
LGpO (chr10) |
7 |
Sat_196 (0.00 cM), Sat_132 (8.75 cM), Sat_318 (24.61 cM), Satt420 (49.71 cM), Satt345 (59.43 cM), Sat_282 (63.81 cM), Sat_108 (129.3 cM) |
Table 3Details of foreground and background selection in different generations.
Table 3
|
Generation |
No. of plants screened |
No. of plants confirmed |
Background selection |
RPGC (%) |
No. of Plants selected based on high % RPGC |
Plants selected based on high % RPGC |
|
|
No. of plants selected |
No. of primers |
|
F1
|
98 |
12 (Lox2lox2) |
- |
- |
- |
- |
- |
|
BC1F1
|
165 |
59 (Lox2lox2) |
24 |
150 |
72.00-83.00 |
5 |
80.00-83.00 |
|
BC2F1
|
127 |
54 (Lox2lox2) |
9 |
51-60 |
84.00-94.33 |
5 |
91.33-94.33 |
|
BC2F2
|
1109 |
250 (lox2lox2) |
35 |
17-26 |
89.33-96.66 |
8 |
94.33-96.66 |
|
BC3F1
|
96 |
31 (Lox2lox2) |
31 |
8-13 |
96.66-98.00 |
5 |
98.00 |
|
BC3F2
|
1200 |
260 (lox2lox2) |
260 |
6 |
96.33-98.66 |
12 |
97.66-98.66 |
Table 4Comparison of the biochemical and agronomic parameters of JS97-52 and JS97-52 derived Lox2-free ILs.
Table 4
|
Genotype |
Dye bleach assay*
|
Lox2 units/g defatted flour |
Protein % |
Days-to-flowering |
Days-to-maturity |
100 SW g |
Yield Kg/ha |
Germination % |
|
|
months |
|
|
0 |
12 |
24 |
|
JS97-52 |
+ve |
450.2b
|
40.2b
|
50b
|
105b
|
9.5b
|
2635b
|
84.6a
|
71.0a
|
30.3a
|
|
PI596540 |
‒ve |
40.00a
|
38.0a
|
28a
|
85a
|
8.4a
|
1256a
|
86.0a
|
85.5b
|
55.0b
|
|
JPILX2F1 |
‒ve |
35.24a
|
39.7b
|
47b
|
103b
|
9.4b
|
2686b
|
87.2a
|
80.4b
|
50.7b
|
|
JPILX2F2 |
‒ve |
39.87a
|
40.0b
|
48b
|
104b
|
9.6b
|
2572b
|
84.4a
|
85.4b
|
50.0b
|
|
JPILX2F3 |
‒ve |
41.39a
|
39.9b
|
47b
|
103b
|
9.2b
|
2589b
|
86.0a
|
85.4b
|
54.4b
|
|
JPILX2F4 |
‒ve |
37.21a
|
40.2b
|
50b
|
104b
|
9.3b
|
2627b
|
87.0a
|
87.3b
|
55.2b
|
|
JPILX2F5 |
‒ve |
38.56a
|
39.0b
|
51b
|
106b
|
9.2b
|
2610b
|
90.1b
|
82.1b
|
54.3b
|
|
JPILX2F6 |
‒ve |
43.78a
|
40.1b
|
48b
|
107b
|
9.5b
|
2589b
|
87.3a
|
90.0c
|
52.3b
|
|
JPILX2F7 |
‒ve |
45.65a
|
39.5b
|
51b
|
103b
|
9.4b
|
2592b
|
90.0b
|
87.3b
|
51.6b
|
|
JPILX2F8 |
‒ve |
38.21a
|
40.0b
|
50b
|
104b
|
9.7c
|
2612b
|
90.2b
|
86.2b
|
50.5b
|
|
JPILX2F9 |
‒ve |
46.21a
|
39.6b
|
48b
|
105b
|
9.4b
|
2691b
|
90.4b
|
84.4b
|
53.4b
|
|
JPILX2F10 |
‒ve |
41.45a
|
40.5b
|
49b
|
102b
|
9.5b
|
2618b
|
90.5b
|
87.6b
|
55.2b
|
|
JPILX2F11 |
‒ve |
38.61a
|
39.7b
|
47b
|
105b
|
9.4b
|
2605b
|
85.1a
|
83.9b
|
49.0b
|
|
JPILX2F12 |
‒ve |
44.32a
|
40.1b
|
50b
|
104b
|
9.4b
|
2598b
|
86.2a
|
82.0b
|
51.3b
|
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