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Summary

10-O-(N,N-dimethylaminoethyl)-ginkgolide B (XQ-1) is an intermediate for synthesizing 10-O-(N,N-dimethylaminoethyl)-ginkgolide B methanesulfonate (XQ-1H), which is a novel ginkgolide B derivative and is being developed as a platelet-activating factor antagonist. A specific and rapid liquid chromatographic method was developed for the quantitative analysis of XQ-1 and its three related impurities, which were 10-O-(N,N-dimethylaminoethyl)-11,12-seco-ginkgolide B (imp-1), 10-O-(N,N-dimethylaminoethyl)-11,12-seco-3,14-dehydroginkgolide B (imp-2) and 10-O-(N,N-dimethylaminoethyl)-3,14-dehydroginkgolide B (imp-3) simultaneously in XQ-1 samples. Chromatographic separation was achieved on a CN band stationary phase, with the mobile phase consisting of methanol and 20 mM dipotassium hydrogen phosphate (pH 7.5) (50:50, υ/υ) in isocratic elution. The flow rate was 1.0 mL min−1 and detector was set at 220 nm. The method was optimized by the analysis of the samples generated during the forced degradation studies. The XQ-1, imp-1, imp-2, and imp-3 were completely separated within 15 min. The resolutions (R s) amongst four target compounds were >2. The developed method was validated with respect to specificity, linearity, accuracy, precision, and robustness. The results indicated that the simultaneous LC determination method was readily utilized as a quality control method for XQ-1 sample.

Open access

Summary

A preparative high-speed countercurrent chromatograph (HSCCC) method for the isolation and purification of C6-C2 natural alcohol and benzyl ethanol from Forsythia suspensa was successfully established. Cornoside, forsythenside F, forsythiaside, and acteoside were rapidly obtained for the first time by HSCCC with a two-phase solvent system ethyl acetate-n-butanol-methanol-water (5:1:0.5:5, υ/υ) in one-step separation. The purities of them were all above 97% as determined by high-performance liquid chromatography, and the combination of ESI-MS and NMR analysis confirmed the chemical structures of the four compounds.

Open access

Summary

Rapid high-performance liquid chromatographic methods with evaporative light scattering detection (HPLC-ELSD) and electrospray ionization multistage mass spectrometry (HPLC-ESI-MSn) have been established and validated for simultaneous qualitative and quantitative analysis of eight steroidal saponins in ten batches of Gongxuening capsule (GXN), a widely commercially available traditional Chinese preparation. The optimum chromatographic conditions entailed use of a Kromasil C18 column with acetonitrile-water (30:70 to 62:38, υ/υ) as mobile phase at a flow rate of 1.0 mL min−1. The drift tube temperature of the ELSD was 102°C and the nebulizing gas flow rate was 2.8 L min−1. Separation was successfully achieved within 25 min. LC-ESI-MSn was used for unequivocal identification of the constituents of the samples by comparison with reference compounds. The assay was fully validated for precision, repeatability, accuracy, and stability, then successfully applied to quantification of the eight compounds in samples. The method could be effective for evaluation of the clinical safety and efficacy of GXN.

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Stripe rust, caused by Puccinia striiformis f. sp. tritici (PST), is one of the most serious diseases of wheat ( Triticum aestivum L.) worldwide. Of 94 Triticum durum/Aegilops tauschii synthetic wheat accessions tested, CI142 (Garza/Boy// Ae. squarrosa 271) was found to be resistant to 6 Chinese PST races. The resistance to stripe rust in CI142 was proven to be controlled by a single dominant gene, tentatively designated YrC142 . Gene postulation showed that the pathogenic specificity of CI142 is different from 21 other lines possessing known resistance genes, such as Yr10, Yr15, Yr24 , and Yr26 , located on chromosome 1B. Bulked segregant analysis (BSA) and F 2 segregation analysis of the CI142/Mingxian 169 cross were used to analyse the SSR markers linked to YrC142 . Five SSR markers were found to be closely associated with YrC142 in the order Xwmc419-YrC142-Xgwm273, Xbarc187-Xgwm18-Xwmc626 , in which the relative genetic distances of these SSR loci to the gene YrC142 were 5.4, 0.8, 0.8, 1.0, and 2.4 cM, respectively. Two SSR markers ( Xgwm273 −162 and Xgwm18 −168 ) distinguished YrC142 from Yr10, Yr15, Yr24 , and Yr26 , suggesting that these 2 SSR markers may be used as diagnostic ones for the gene in a wheat breeding program against stripe rust. Based on these findings, YrC142 is most likely a new gene or a new allele at the Yr26 locus, which provides an opportunity to diversify stripe rust-resistant resources for wheat breeding programs.

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The presence and frequency of the resistance gene complex Lr34/Yr18 was investigated in the wheat breeding programme of the Agricultural Research Institute, Martonvásár, Hungary. A total of 226 wheat cultivars and advanced lines from Hungary and other countries were tested with an STS marker, csLV34 , to understand the distribution of the Lr34/Yr18 resistance gene complex. A 150-bp PCR fragment was amplified in 64 wheat cultivars and lines with the resistance genes Lr34/Yr18 , while a 229-bp fragment was detected in 162 genotypes without Lr34/Yr18 . The genotypes with Lr34/Yr18 accounted for 28.3% of the wheat cultivars and advanced lines tested. Among the 128 varieties and breeding lines of Martonvásár origin tested, 34 carried the Lr34/Yr18 genes, with a frequency of 26.6%. The frequency of these genes was 30.6% in genotypes of other origin. The STS marker csLV34 could be used as an effective tool for the marker-assisted selection of Lr34/Yr18 genes in breeding wheat cultivars with durable rust resistance.

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Youzimai is a widespread wheat landrace and has been used extensively in breeding programs in China. In order to assess the genetic variation between and within Youzimai accessions, samples of 31 landrace accessions of wheat, all called ‘Youzimai’, were collected from 6 geographic regions in China and evaluated using morphological traits, seedling resistance to powdery mildew, gliadin and microsatellite markers. Typical differences among accessions were observed in morphological characteristics. Forty-five (58.4%) of 77 assayed SSR markers showed polymorphism over the entire collection and total 226 alleles were identified with an average of 5.02 alleles per locus. SSR data indicated that the accessions from Hebei province were the most diverse, as evidenced by greatest number of region-specific alleles and highest diversity index. These accessions, therefore, probably experienced the most substantial morphological and molecular evolution as a result of various natural and anthropomorphic influences. On the other hand, differentiation in gliadin phenotypes was found among seeds within 80.6% of total accessions and average 61.5% of entire collections showed heterogeneous and comprised resistant plants in reaction to powdery mildew, suggesting the presence of a wide diversity within the wheat landrace. By developing an intimate knowledge of the available wheat genotypes, appropriate selections can be made for commercial application in order to conserve and exploit the diversity of the wheat landraces.

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Purple pericarp is an interesting and useful trait in Triticum aestivum, but the molecular mechanism behind this phenotype remains unclear. The allelic variation in the MYB transcriptors is associated with the phenotype of pigmented organs in many plants. In this study, a MYB transcription factor gene, TaMYB3, was isolated using homology-based cloning and a differentially expressed gene mining approach, to verify the function of the MYB transcriptor in the purple pericarp. The coding sequence of TaMYB3 in cultivar Gy115 was the same as that in cultivar Opata. TaMYB3 was localized to FL0.62–0.95 on chromosome 4BL. The TaMYB3 protein contains DNA-binding and transcription-activation domains, and clustered on a phylogenetic tree with the MYB proteins that regulates anthocyanin and proanthocyanin biosynthesis. TaMYB3 localized in the nuclei of Arabidopsis thaliana and wheat protoplasts after it was transiently expressed with PEG transformation. TaMYB3 induced anthocyanin synthesis in the pericarp cells of Opata in the dark in collaboration with the basic helix–loop–helix protein ZmR, which is also the function of ZmC1. However, TaMYB3 alone did not induce anthocyanin biosynthesis in the pericarp cells of the white grain wheat cultivar Opata in the light after bombardment, whereas the single protein ZmR did. Light increased the expression of TaMYB3 in the pericarp of Gy115 and Opata, but only induced anthocyanin biosynthesis in the grains of Gy115. Our results extend our understanding of the molecular mechanism of the purple pericarp trait in T. aestivum.

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A reborn interest has occurred during the last decade toward wheat landraces for broadening genetic basis of modern wheat cultivars. The investigation of molecular traits within and between existing landraces of wheat can help scientists to develop appropriate strategies for their efficient maintenance and exploitation. The present study dealt with the gliadin characterization of forty-seven wheat landraces collected from wheat mainly planted areas of China, each of which was represented by a sample of at least 43 individuals. Twelve accessions selected on the basis of gliadin analysis were investigated further using 21 SSR markers. The results proved that landraces of wheat are a mixture of variable individuals genetically distinguishable from each other. Twelve of the analyzed 47 accessions were observed to be homogeneous, while 35 (74.5%) of them were heterogeneous in their gliadin composition. In total, 122 gliadin pattern were observed. On average, 10.1% (Gst) of the total variation arose from differentiation among regions, and 89.9% was attributed to within-region variation. Furthermore, nineteen of the 21 SSR markers were polymorphic across all the populations. The total number of the amplified DNA products was 110, with a mean of 6.11 alleles per locus. The values of genetic diversity within each landrace population varied from 0.006 to 0.351. Implications for the management of this valuable genetic resource are discussed.

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Cereal Research Communications
Authors:
L. Zhang
,
Z. Yan
,
S. Dai
,
Q. Chen
,
Z. Yuan
,
Y. Zheng
, and
D. Liu

Two experiments to investigate the crossability of Triticum turgidum with Aegilops tauschii are described. In the first experiment, 372 wide hybridization combinations were done by crossing 196 T. turgidum lines belonging to seven subspecies with 13 Ae. tauschii accessions. Without embryo rescue and hormone treatment, from the 66220 florets pollinated, 3713 seeds were obtained, with a mean crossability percentages of 5.61% which ranged from 0 to 75%. A lot of hybrid seeds could germinate and produce plants. Out of 372 combinations, 73.12% showed a very low crossability less than 5%, 23.39% showed the crossability of 5–30%, 2.69% showed the crossability of 30–50%, 0.81% showed high crossability more than 50%, respectively. Among the seven T. turgidum subspecies, there were significant differences in crossability. The ssp. dicoccoides and dicoccon showed the highest crossability, while polonicum the lowest. All the crossability percentages more than 30% were obtained from the crossing of ssp. dicoccoides or dicoccon with Ae. tauschii .In the second experiment, the genetics of crossability was investigated using T. turgidum ssp. durum cultivar Langdon and the D-genome disomic substitution lines of Langdon. Compared with the control Langdon, lines 7D(7A) and 4D(4B) showed higher crossability, which suggested that chromosomes 7A and 4B of tetraploid wheat cv. Langdon carried dominant alleles inhibiting crossability with Ae. tauschii . The relationships of present results with previously reported crossability genes of wheat are discussed.

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Journal of Thermal Analysis and Calorimetry
Authors:
Z. Xiao
,
D. Liu
,
C. Wang
,
Z. Cao
,
X. Zhan
,
Z. Yin
,
Q. Chen
,
H. Liu
,
F. Xu
, and
L. Sun

Abstract  

The effect of mechanical alloying on Zn-Sb alloy system is investigated with X-ray diffraction (XRD), laser grain size analysis and differential scanning calorimetry (DSC) respectively. The results of laser particle size analysis shows that the particle size decreases with increasing of the grinding time between 0 and 24 h. XRD and DSC results indicate that longer the grinding time of Zn-Sb is, the more content of Zn4Sb3 become in the product in this process.

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