Proposal for the identification of barley varieties based on the genotypes for 2 hordein and 39 isoenzyme loci of 47 reference varieties

Summary Fifty-nine spring and 7 winter barley varieties in The Danish List of Varieties of Agricultural Crops, 1983/84 were examined for variation at 39 isoenzyme and two hordein loci. Twenty-three isoenzyme loci had one allele only, and 16 loci had from two to five alleles. One hordein locus had 12 and the other 15 alleles. The variation in the 16 enzyme loci permitted the division of the 66 varieties into 63 groups, while the two hordein loci produced 34 groups. A study of 20 individuals from each variety showed that 22 varieties were polymorphic in at least one locus. Eight starch gel electrophoresis with various buffer systems, one agar gel electrophoresis (for amylases), and one polyacrylamide gel electrophoresis (for hordein) were performed to develop the patterns associated with the 41 loci. The polyacrylamide gel electrophoresis developing hordein patterns was clearly the most powerful single system for identifying barley varieties because of the large number of alleles.     

Cytological and Isozyme Evaluation of Tall Fescue × Italian Ryegrass Hybrids

Development of tall fescue (Festuca arundinacea Schreb., 2n = 6x - 42) × Italian rye-grass (Lolium multiflorum Lam., 2n = 2 ×= 14) hybrids would enhance efforts to improve the quality of tall fescue. Two ‘Kentucky 31’ tall fescue בLemtal Italian ryegrass hybrids were obtained via embryo rescue on MS media containing casein hydrolysate, ascorbic acid and sucrose. Chromosome pairing at metaphase I had an average of more than 12 bivalents per cell. Since Festuca-Lolium pairing can account only for seven of the paired chromosomes, intergenomic as well as interspecific chromosome pairing is indicated. There was no cytoplasmic effect on chromosome pairing. To determine if enzymes could be used as genetic markers for distinguishing hybrids from self-contaminants in crosses, zymograms of PGI, 6-PGD, MDH, GOT and ACPH were obtained from parents and hybrids using starch gel etectrophoresis. PGI, 6-PGD and MDH had fewer bands in the diploid ryegrass, as compared with the hexaploid tall fescue and the tetraploid hybrid.     

Determination of leghemoglobin components and xylem sap composition by capillary electrophoresis in hypernodulation soybean mutants cultivated in the field

The hypernodulation soybean mutant lines (NOD1-3, NOD2-4, NOD3-7) and their parent Williams, and the mutant En6500 and its parent Enrei were cultivated in a sandy dune field in Niigata, and the nodules and root bleeding xylem sap were sampled at 50, 70, 90, and 120 d after planting (DAP). The nodule size distribution patterns and concentration of leghemoglobin components were determined. The number of nodules of the hypernodulation mutant lines was about two to three times higher than that of the parent lines irrespective of the sampling date. At 50 DAP the nodule size was relatively smaller in the hypernodulation mutant lines, and the total dry weight of the nodules was almost the same in the mutant lines and their parents. At 70 DAP and 90 DAP, the size distribution of the hypernodulation mutant nodules became .almost the same as that of the parent lines, and both the number and total dry weight of the nodules were higher than those of the parent lines. The concentration of four Lb components was separately measured by capillary electrophoresis. The concentration of the Lb components in the hypernodulation mutant lines tended to be lower than in the parents, but the component ratios were not different between the hypernodulation mutants and their parents. Under field conditions, plant growth and nodulation characteristics were more similar between mutants and parents than in the hydroponic culture reported previously, although the mutants did exhibit hypernodulation traits. These findings suggest that the decrease in the Lb concentration and the different Lb components ratios in the mutants may be caused by secondary effects of excess nodulation, such as photosynthate deficiency, rather than by a genetic defect in mutation. The concentration of major nitrogenous compounds (allantoic acid, allantoin, asparagine, aspartic acid, and nitrate) in the xylem sap was also measured by capillary electrophoresis. The concentration of ureides and nitrate in xylem sap decreased with the plant age, but the asparagine concentration increased during the same period. The concentrations of ureides and asparagine were higher, and the nitrate concentration was lower in the mutant lines than in their parents, possibly due to the higher dependence on N₂ fixation than N0₃ ^- utilization. In the xylem sap, nitrate was the major inorganic anion followed by phosphate, sulfate, and chloride, and potassium was the major cation followed by calcium or magnesium and sodium.     

40m游艇艇艏砰击压力有限元分析

为了研究艇艏横倾时的砰击状况,采用数值模拟的方法对一艘长40 m钢制游艇的艇艏砰击性能进行了分析.在验证有限元方法模拟船舶入水砰击的基础上,利用ANSYS/LS-DYNA软件建立船艏二维有限元模型,分析了游艇不同入水速度和横倾角对艇艏砰击压力的影响规律,数值模拟结果为预报艇艏的砰击压力状况提供依据,为游艇的结构设计提供参考价值.     

新疆军垦型细毛羊MHC基因临近区段3个遗传标记的研究

比较基因组学是基因组学的重要分支,现已成研究生物基因组的最重要的策略与手段.研究发现绵羊与牛及山羊之间基因组序列的同源性或同线性程度要高于其他物种,能利用牛和山羊的基因组研究结果进行比较基因组学研究,进而阐明绵羊的基因组功能.试验采用琼脂糖凝胶电泳技术,对新疆军垦型细毛羊20号染色体MHC基因邻近区段的DMB_EX2、MCMA36、CP73 三个分子标记分别进行了PCR产物的检测、测序和同源性比对.结果表明,这3个序列均与相关物种的对应序列具有很高的同源性:DMB_EX2与牛的对应序列的同源性为89;,MCMA36与山羊的对应序列的同源性为97;,CP73与羊的对应序列的同源性为96;.     

不同提取方法及上样量对牡丹试管苗茎基部蛋白双向电泳的影响

为建立一套适合于牡丹试管苗茎基部蛋白的双向电泳技术,以便更好地利用蛋白质组技术研究牡丹试管苗不定根的发生机理,本研究比较了三种不同蛋白质提取方法对双向电泳结果的影响,并在蛋白质上样量方面进行了比较。结果表明,乙酸铵/甲醇酚提取法所得2-DE图谱的蛋白点很少,仅检测到45个,且较模糊,有明显的拖尾现象,分辨率很低;乙醇/乙醚丙酮法所得的蛋白点也较少（101个）,较模糊,且横竖纹干扰较大;三氯乙酸/丙酮法所得蛋白点数较多,可检测到434个清晰的蛋白点,且形状规则,重复性好,适合后续分析,操作也较为简便。用三氯乙酸/丙酮法提取蛋白,采用800μg、1000μg和1200μg三个不同的上样量进行双向电泳,在上样量为1200μg时（IPGpH3～10,24cm）,蛋白质在12%SDS-PAGE胶上得到了较好的分离,在2-DE图谱上可分辨出562个蛋白点。因此,三氯乙酸/丙酮法是较适合于牡丹试管苗茎基部蛋白质提取的方法,1200μg是较为合适的上样量。     

Characterization of the 1B/1R translocation in wheat using water extractable protein concentrate

Summary An electrophoretic procedure was developed to obtain patterns of water soluble proteins from the endosperm halves of seeds to detect the 1B/1R translocation in wheat cultivars. The water soluble proteins were precipitated with Coomassie Brilliant Blue R-250 and separated in a 10% polyacrylamide gel with sodium dodecyl sulfate. This procedure extracted protein bands (Mr 40,000, 44,000 and 45,000) corresponding to the -secalins of the rye parent which were present only in the wheat cultivars carrying 1B/1R translocation. By simplifying extract preparation and providing clear band resolution this procedure facilitates large scale screening of wheat lines for the rye translocation. Proteins with properties of overlapping solubilities are also discussed.Abbreviations CBB - Coomassie Brilliant Blue - DDW - deionized distilled water - DTT - dithiothreitol - HMW - high molecular weight - PAGE - polyacrylamide gel electrophoresis - Mr - relative molecular mass - SDS sodium dodecyl sulfate Contribution 1569 of Agriculture and Agri-Food Canada, Research Centre, Winnipeg, Canada     

Community structure of methanogenic archaea in paddy field soil under double cropping (rice-wheat)

Community structure of methanogenic archaea in paddy field soil under double cropping (rice [Oryza sativa L.] and wheat [Triticum aestivum L.]) was studied by the denaturing gradient gel electrophoresis (DGGE) method. Soil samples under flooded and upland conditions were collected 7 and 6 times, respectively, from two paddy fields throughout a year, and two primer sets, 0357F-GC/0691R and newly designed 1106F-GC/1378R, were used for DGGE analysis. The 25 and 29 different bands were observed on the DGGE gels with the primers 0357F-GC/0691R and 1106F-GC/1378R, respectively. DGGE band patterns of the methanogenic archaeal community were stable throughout a year including the cultivation periods of rice under flooded conditions and of wheat under upland conditions. Cluster analysis and principal component analysis suggested that the difference in the soil type (sampling region) largely influenced the community structures of methanogenic archaea in paddy field soil, while the effects of sampling period and different fertilizer treatments on them were small. Most of the sequences obtained from the DGGE bands were closely related to Methanomicrobiales, Methanosarcinaceae, Methanosaetaceae and Rice cluster-I.     

Seed Storage Proteins of Triticum turgidum ssp. dicoccoides and Their Effect on the Technological Quality in Durum Wheat

F₄ progenies of a cross between durum wheat cultivar ‘Creso’ and an accession of Triticum turgidum ssp. dicoccoides with high protein content were analysed by two different electrophoretic procedures (A-PAGE and SDS-PAGE). Variation of storage proteins at the Glu-A1, Glu-B1, Glu-B3 and Gli-B1 loci was studied. Electrophoretic analyses have shown that parents contain different alleles at each of the four loci considered and that protein components of T. dicoccoides are uncommon among cultivated wheats. Recombination between the Glu-B3 and Gli-B1 loci was observed. To determine the effects of the allelic variants on gluten properties, F₅ grains from every F₄ line were analysed for protein content and SDS-sedimentation value. Gluten quality was strongly associated with the allelic type of proteins coded by the Glu-B3 locus and, to a lesser extent, to those coded by Glu-A1. Mean sedimentation value of progenies possessing the ‘Creso’Glu-B3 allele was significantly greater than that showing the T. dicoccoides allele. High molecular weight glutenin sub-units coded by the T. dicoccoides Glu-A1 locus were also associated with larger sedimentation values than null form of ‘Creso’. Results of SDS-test, obtained for recombinants between Glu-B3 and Gli-B1, confirmd that specific omega- and gamma-gliadins are only genetic markers of quality, whereas variation for LMW glutenin subunits coded at Glu-B3 is responsible for differences in gluten properties.     

Seed of Ullucus tuberosus—An apomict or not

Summary The paper deals with variations in enzyme pattern in the seeds of ulluco, Ullucus tuberosus. Six seeds per clone, four clones and three enzyme systems (malate dehydrogenase, glutamate oxaloacetate transaminase and 6-fosfoglucose dehydrogenase) were examined. There was variation in enzyme pattern between the seeds of a single clone. It is concluded that ulluco is not an apomictic species but a truly sexual one. Consequences of these findings for breeding programmes of ulluco are pointed out.