PLANT REGENERATION FROM IMMATURE COTYLEDONOUS TISSUE CULTURES OF SOYBEAN BY SOMATIC EMBRYOGENESIS

Genetic engineering of soybean is limited because of the difficulty of regeneration of plants via in vitro culture. Here we report that a method of obtaining somatic embryos and regenerated plants of soybean has been developed. It is achieved by culturing immature cotyledons of soybean on modified Murashige-Skoog medium supplemented with high concentration of either napthalene acetic acid (NAA) or 2,4-dichlorophenoxyacetic acid (2,4-D). High induction frequencies of 85% and 94% are reached by using 10mg/l NAA and 5mg/l 2,4-D, respectively. A number of regenerated plantlets of soybean are transplanted to sterilized soil and grown into 15 full plants in pots.     

Osmotic regulation of 10 wheat (Triticum aestivum L.) genotypes at soil water deficits

Drought is a worldwide problem, seriously influencing plant (crop) productivity. Wheat is a stable food for 35% of the world population, moreover about 60% of land area on the globe belongs to arid and semi-arid zone. Wheat drought resistance is a multi-gene-controlling quantitative character and wheat final production in field is realized mainly by physiological regulation under the condition of multi-environmental factor interaction. Exploring drought resistance physiological mechanisms for different wheat genotypes is of importance to finding new drought resistance gene resources and conventional breeding and the basis for wheat drought resistance biotechnological breeding and platform. Osmotic adjustment regulation is the main component for physiological machinery of wheat drought resistance. By pot-cultivating experiments, investigation of osmotic adjustment comparison for 10 wheat genotypes at soil water deficits (75% FC, 55% FC, 45% FC, respectively), was conducted. The main results were as followed: (1) K⁺ content in 10 wheat genotypes at three levels of soil water stress and at the same soil water deficit was very different. Five of these 10 wheat genotypes had higher K K⁺ content under the condition of 75% FC. (2) Five of these 10 wheat genotypes possessed greater soluble sugar content at 55% FC soil water level. (3) Proline (Pro) content in five wheat genotypes was higher at 75% FC. (4) Five of these 10 wheat genotypes had lower malondialdehyde (MDA) content at 45% FC at seedling stage. Osmotic adjustment of wheat different genotypes was discussed in terms of different content of osmotic solutes.     

Investigation on dynamic changes of photosynthetic characteristics of 10 wheat (Triticum aestivum L.) genotypes during two vegetative-growth stages at water deficits

Drought is a worldwide problem, seriously influencing plant (crop) productivity. Wheat is a stable food for 35% of the world population, and moreover, about 60% of land area on the globe belongs to arid and semiarid zone. Wheat drought resistance is a multi-gene controlling quantitative character and wheat final production in field is realized mainly by physiological regulation under the condition of multi-environmental factor interaction. Exploring drought resistance physiological mechanisms for different wheat genotypes is of importance to finding new drought resistance gene resources and conventional breeding, and the basis for wheat drought resistance biotechnological breeding and platform. Photosynthesis is the main component for physiological machinery of wheat assimilates conversion and wheat production. Investigation on photosynthetic characteristics of different wheat genotypes at soil water deficits also has other implications for refine physiological regulation of photosynthesis in fields and field management of crops in arid and semiarid areas. By pot-cultivating experiments, investigation of photosynthesis for 10 wheat genotypes at seedling stage and tillering stage at soil water deficits (75%FC, 55%FC and 45%FC, respectively) was conducted. The main results were as followed: developmental stages influenced wheat photosynthesis greatly and tillering stage played more roles; there were significant difference in the main photosynthetic parameters, photosynthesis rate (Photo), stomatal conductance (Cond) and transpiration rate (Tr), among 10 wheat genotypes; general photosynthesis and drought resistance in different wheat genotypes was related much to their domesticated origin soil water environment and selected generations and there was a photosynthetic threshold effect in terms of different wheat genotypes at soil water deficits.     

Capillary electrophoresis separation of high molecular weight glutenin subunits in bread wheat (Triticum aestivum L.) and related species with phosphate-based buffers

This study focused on optimizing phosphate-based buffers and other capillary electrophoresis (CE) parameters for separating and characterizing high molecular weight glutenin subunits (HMW-GS) in bread wheat (Triticum aestivum L., AABBDD, 2n = 6x = 42), emmer (Triticum dicoccum, AABB, 2n = 4x = 28) and Aegilops tauschii (DD, 2n = 2x = 14). The fast and high-resolution separation of HMW-GS was achieved using 0.1 M phosphate-glycine buffer (pH 2.5, containing 20% acetonitrile and 0.05% hydroxypropylmethylcellulose) at 12.5 kV and 40 degrees C with 25 microm inside diameter (ID)x27 cm uncoated fused-silica capillary. In general, one sample separation can be analyzed in 15 min. The good run-to-run repeatable separation of HMW-GS could be obtained with a relative standard deviation of less than 1% when capillaries were rinsed with 1 M phosphoric acid for 2 min, followed by separation buffer for 2 min after each separation. The HMW-GS from some bread wheat cultivars as well as tetraploid and diploid accessions was separated by the CE method described above, and all subunits detected were well characterized and readily identified. Some HMW-GS showed reversed mobilities and elution order compared to the methods of sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and SDS-CE. Particularly, most of the HMW-GS analyzed with the CE buffer used were separated into multiple peaks, generally a high peak plus a minor peak. CE appears to be capable of separating and characterizing HMW-GS with fast and high-resolution features, therefore it is expected to be useful for specific germplasm screening and desirable HMW-GS identification in wheat quality improvement.     

STRUCTURE OF THE MITOCHONDRIAL URFA6L GENE AND tRNA~(Lys) GENE FROM CARP

The carp mitochondrial URFA6L gene consists of 165 base pairs. The overall structural organization of the gene is very similar to that of the Xenopus URFA6L gene. Their nucleotide sequences exhibit 68% homology. The carp URFA6L gene encodes a protein of 54 amino acids. The amino acid composition of the protein is unusual because almost half of the residues consist of 5 hydrophobic amino acids(proline, tryptophan, leueine, isoleueine and tyrosine). A comparison between the amino acid sequences of 5 vertebrate URFA6L proteins and the yeast ATPase8 showed that they have weak but very important common structural features, suggesting that the vertebrate URFA6L proteins may function asATPase8. The nucleotide sequence of the lysine tRNA gene from carp has been determined and represented in cloverleaf secondary structure. Similar to amphibian and mammalian mitochondrial tRNA~(Lys) genes, the carp mitochondrial tRNA~(Tys) gene also has some unusual structural features as compared with its cytoplasmic counterpart