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Complete nucleotide sequences of two soybean mosaic virus strains differentiated by response of soybean containing the Rsv resistance gene.

The complete nucleotide sequence of the genomic RNAs of strains G2 and G7 of soybean mosaic virus were determined. In both cases, the genome is 9588 nucleotides long, excluding the 3'-terminal poly(A) sequence. A large open reading frame (nucleotides 132 to 9329) encodes a polyprotein of 3066 amino acids with a predicted M(r) of either 349542 (strain G2) or 349741 (strain G7). Based on comparison with the proposed locations of cleavage sites of other potyvirus polyproteins, nine mature proteins are predicted. The mature proteins of the two strains share 94 to 100% amino acid identity, with the greatest variability occurring in the 35K and 42K proteins. Differences in local net charge in portions of these proteins as well as differences in amino acid sequence throughout the genome are discussed in relation to resistance and susceptibility of host plants to strains G2 and G7. Comparison with other potyviruses may be useful for taxonomic clarification of viruses and strains.

Amino Acid Sequence↗

Soybean protoplast culture and direct gene uptake and expression by cultured soybean protoplasts.

A method was developed for culturing protoplasts freshly isolated from developing soybean (Glycine max L.) cotyledons. First cell divisions were observed within 5 days after protoplast isolation and microcalli, consisting of about 20 cells, were formed within 10 days. Thirty days after protoplast isolation, callus tissues were observed without the aid of a microscope. A 30 to 50% plating efficiency was consistently obtained. Using a polyethylene glycol-electroporation technique, DNA was introduced into these protoplasts. The protoplasts were then cultured to form callus. Chloramphenicol acetyltransferase (CAT) activity was detected in protoplast cultures 6 hours after introduction of a 35S-CAT-nopaline synthase 3' chimeric gene. The highest CAT activity was detected in 3-day-old electroporated protoplast cultures, indicating transient expression of the introduced gene. Some CAT activity was detected in 40-day-old callus cultures and in geneticin (G418) selected callus tissues which also received a chimeric neomycin phosphotransferase II gene, indicating the presence of stable transformants. A control chimeric gene with an inverted 35S promoter failed to produce any CAT activity in this system.

Journal Article↗

1,1-Diphenyl-2-picrylhydrazyl radical-scavenging compounds from soybean miso and antiproliferative activity of isoflavones from soybean miso toward the cancer cell lines.

Guided by their DPPH radical-scavenging activity, nine compounds were isolated from soybean miso. Of these, 8-hydroxydaidzein, 8-hydroxygenistein and syringic acid had as high DPPH radical-scavenging activity as that of alpha-tocopherol. The antiproliferative activity of four of the isolated isoflavones toward three cancer cell lines was examined. 8-Hydroxygenistein showed the highest activity (IC50=5.2 microM) toward human promyelocytic leukemia cells (HL-60).

Animals↗

Properties of rice cooked with commercial water-soluble soybean polysaccharides extracted under weakly acidic conditions from soybean cotyledons.

It has been found that commercial water-soluble soybean polysaccharides (SSPS) can make cooked rice and noodles non-sticky and prevent rice grains and noodles from adhering to each other. We studied in detail the phenomenon of rice cooked with SSPS. We assumed that the phenomenon resulted from the interaction between SSPS and starch during cooking, and studied the effects of SSPS on the gelatinizing behavior of rice starch by using a Rapid-Visco-Analyzer. The addition of SSPS reduced the viscosity of the gelatinized starch. This lower final viscosity of the rice starch was more distinct from than that of potato starch. These results imply that the properties of SSPS in forming a non-sticky condition might result from a decrease in the viscosity of the gelatinized starch.

Adhesiveness↗

Nitrogen balance and amino acid disappearance from the small intestine in calves fed soybean meal-, toasted soybean meal- or corn gluten meal-supplemented diets.

Nine crossbred (Hereford X Angus X Charolais) heifer calves (139 kg; 6 mo of age) with abomasal and ileal cannulas were used in a repeated design to evaluate N balance and amino acid disappearance in the small intestine. Calves were fed either soybean meal (SBM), toasted SBM (TSBM, 93 C for 90 min) or corn gluten meal (CGM) as supplemental protein sources. Each calf received approximately 83 g N/d from a cottonseed hull-corn based diet with 43% of the total dietary N supplied by the test proteins. Each experimental period consisted of a 10-d adaptation, 6-d digesta collection and 5-d excreta collection. Following the first 21-d period, calves were randomly re-allotted to treatment and the sampling process was repeated. Dry matter (64%) and N digestibilities (61%) and N retention (36.8 g/d) were similar (P greater than .10) among treatments. Nitrogen flow to the small intestine was similar for TSBM- and CGM-fed calves (119.1 g/d), but greater (P less than .01) than for those offered SBM (96.3 g/d). Offering TSBM and CGM resulted in greater quantities of essential, nonessential and total amino acids reaching the abomasum compared with SBM. Total amino acid flow to the small intestine was 100, 120 and 128% of intake for SBM, TSBM and CGM, respectively. Numerically, amino acid digestibility was lower in CGM-fed calves. Methionine digestibility was highest (64.6%), while histidine was lowest (43.7%). Feeding CGM may result in greater quantities of amino acids reaching the small intestine; however, several of these amino acids may be less digestible than for TSBM.

Amino Acids↗

Induced non-enzymatic browning of soybean meal. III. Digestibility and efficiency of protein utilization by ruminants of soybean meal treated with xylose or glucose.

Trials were conducted to evaluate effects of non-enzymatic browning of soybean meal (SBM) on efficiency of protein utilization and N digestibility. In trial 1, 48 Suffolk-Finnsheep lambs (22 kg) were fed 80 d to evaluate efficiency of protein utilization for growth when supplemental protein was fed as urea (U), commercial SBM (CS), or commercial SBM (pH 8.5, 83% dry matter) containing xylose (3 mol/mol SBM-lysine) and heated 30 min (XTS-30) or 55 min (XTS-55). Diets containing graded levels of N from CS, XTS-30 and XTS-55 were fed. Response criterion was efficiency of protein utilization, plotted as gains of lambs fed test proteins minus gain of lambs fed U vs supplemental test protein fed. Efficiencies of protein utilization were .62, 1.27 and .91 for CS, XTS-30 and XTS-55, respectively. Protein from XTS-30 was used more efficiently (P less than .05) than that from CS. In trial 2, apparent digestibility of N from CS (97%) was higher (P less than .01) than XTS-30 (77%) and XTS-55 (82%) by Suffolk-Finnsheep lambs (27 kg). In trial 3, 60 mixed-breed steers (218 kg) were fed individually for 105 d to evaluate glucose as a reducing sugar. Glucose-treated SBM (GTS) was prepared by mixing glucose (3 mol/mol SBM lysine) with SBM, adjusting pH and dry matter content to 8.5 and 80%, respectively, and heating at 150 C for 60 min. Supplemental N sources were U, CS, GTS and a 50:50 mixture (protein basis) of corn gluten meal and blood meal (CGM/BM).(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Feed↗

Effects of ethanol and heat treatments of soybean meal and infusion of sodium chloride into the rumen on ruminal degradation and escape of soluble and total soybean meal protein in steers.

Soybean meal (SBM) treated with 70% ethanol at 80 C (ET), nontreated SBM (NT) or a ureacasein-corn mix (UC) was fed to steers fitted with ruminal and duodenal cannulae to study ruminal N metabolism. Sodium chloride (NaCl) was ruminally infused at 0 or 500 g/d. Nitrogen supplements provided approximately 70% of total dietary N. Experimental design was a 6 X 6 Latin square with a 3 X 2 factorial arrangement of treatments. Total duodenal N flows and non-ammonia, non-bacterial-N (NANB-N) flows were higher (P less than .05) when steers were fed SBM treatments compared with UC, and higher (P less than .05) when steers were fed ET compared with NT. Percentage of SBM-N escaping ruminal degradation was greater (P less than .05) when steers were fed ET compared with NT, and greater (P less than .05) when NaCl was infused into the rumen. Duodenal flows of total, indispensible and dispensible amino acids were increased (P less than .05) when steers were fed SBM treatments compared with UC, and greater (P less than .05) when steers were fed ET compared with NT. No differences in soluble N flows at the omasum were observed due to treatment. Bacterial protein comprised the majority of the N leaving the rumen. Both ruminal NaCl infusion and ethanol and heat treatment of SBM increased ruminal SBM-N escape.

Animals↗

[Laboratory performance study of the quantitative detection method for genetically modified soybeans (roundup ready soybeans 40-3-2)].

To investigate important factors affecting the analytical results, a laboratory-performance study was attempted for the Japanese official methods to detect genetically modified (GM) soybeans (40-3-2). Test samples containing 0, 1 and 5% GM soya powder in non-GM soya powder was prepared. A set of 3 test samples was sent to the participating laboratories along with the protocol. The data were collected from all laboratories and statistically analyzed. In the real-time PCR detection method, the average values of the GM 1% and 5% samples were both much lower than the spiked value because the laboratories using a silica-membrane DNA extraction method underestimated the GM value. On the other hand, the laboratories using other extraction methods, such as the CTAB method obtained values close to the spiked value. These results suggest that use of the silica-membrane DNA extraction method may result in underestimation of the GM content in the real-time PCR method. In the ELISA method, the average value of 5% spiked samples appears to be slightly higher than the fortified value. But, overall, it was considered that reported values were close to the spiked level.

DNA, Plant↗

[Transgenic soybean obtained with Agrobacterium tumefaciens-mediated transformation of embryonic tip of soybean mature seeds].

Regenerated embryonic tips were inoculated with Agrobacterium tumefaciens strain EHA105, which contains binary vector pCAMBIA2301, and cultured for 20 h. Our results showed that the T-DNA transfer efficiency reached up to 63.3% (Table 1) and the transformation efficiency reached up to 6.4%-12.1% (Table 2). The effect of infection time on T-DNA delivery into soybean embryonic tips was determined (Table 1). We also discuss the effects of days of co-cultivation to transient expression and the effects of different AS concentrations to transient expression of gus gene (Figs. 1,2). These data indicate that the embryonic tip regeneration system can be used for efficient, effective Agrobacterium-mediated transformation.

Agrobacterium tumefaciens↗

Abomasal infusion of soybean meal necessary to provide nitrogen retention equivalent to steer fed soybean meal.

Eight growing Angus steer calves averaging 213 kg were fitted with abomasal infusion cannulae to compare feeding 455 g of soybean meal (SBM) daily with infusing 120 g SBM abomasally (26% of intake) on nitrogen (N) retention and plasma urea and amino acid levels. A reversal design was used in which each steer received a SBM-supplemented diet plus water abomasally and an unsupplemented diet (basal) plus 120 g of SBM infused abomasally. Feeding a normal intake of SBM or infusing 26% of SBM intake post-ruminally (abomasally) resulted in similar daily N retention (18.4 g N for fed steers and 18.8 g N for infused steers). Total urinary output (liter/day), as well as urinary N losses (g/day), was 6.8 vs. 5.2 and 44.1 vs. 24.0 for the fed and infused groups of steers, respectively (P less than .05). Nitrogen retained expressed as a percent of N intake was 7.2% higher for SBM infusion. Daily fecal dry matter excretion was .25 kg greater for steers infused with SBM. Plasma urea levels were higher (P less than .05) for SBM-fed steers at each 2-hr sampling interval for 8 hr after feeding. Plasma free amino acid levels were similar for both groups of steers.

Abomasum↗