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41.
Wang Zunxin Wang Xianyu Liu Siqin Yang Ying Li Yang Chen Siyuan Wang Guangpeng Zhang Xincheng Ye Yuxiu Hu Laibao Zhou Qing Wang Feibing Chen Xinhong 《Journal of Plant Growth Regulation》2023,42(1):294-303
Journal of Plant Growth Regulation - Zinc is an important micronutrient for the growth and development of human body and plants. Proper use of nitrogen fertilizer and foliar application of Zn have... 相似文献
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别藻蓝蛋白藻蓝胆素发色团分子构象研究 总被引:1,自引:0,他引:1
主要研究了蓝绿藻污棕席藻(Phormidium luridum)别藻蓝蛋白在不同 pH值条件下的吸收光谱和共振拉曼光谱.发现低聚化的结果导致了三聚体别藻蓝蛋白 650nm 特征吸收峰的消失和一些共振拉曼带强度和位置的移动.结果表明在低 pH 值作用下的低聚化的别藻蓝蛋白中藻蓝胆素发色团分子的构象和自由胆素分子类似,比三聚体的别藻蓝蛋白的发色团分子更趋于卷曲,折叠的构象态.而三聚体的别藻蓝蛋白,主要的拉曼带 1645cm-1是其发色团分子构象处于更线性延展的标志,其光谱行为和吸收光谱 Avis/Auv所表征的发色团分子构象的结果相一致. 相似文献
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本文研究一类含人口迁移的性传染病模型,应用摄动方法和定性方法研究平衡点的稳定性和迁移率的影响。普举例说明。 相似文献
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Xiong Zhang Ming-You Peng En-Ming Feng Qing-Dan Li Lu Chen Hu-Cheng Yang Bing Guo Hong Liang Ying-Tong Di Lei Tang Ying Yan 《化学与生物多样性》2023,20(10):e202301061
Three previously undescribed diterpenoids, helioscopnoids A–C, and eight known compounds were isolated from the whole plants of Euphorbia helioscopia. Their structures were established by extensive analysis of spectra and data comparison with previous literatures. Among them, compound 4 was identified as 24,24-dimethoxy-25,26,27-trinoreuphan-3β-ol with revised configurations of C-13, C-14, and C-17 (13R*, 14R*, 17R*). Cytotoxicity assays revealed that all compounds exhibited varying levels of cytotoxicity against H1975 cells, with compound 9 displaying the most potent activity, as indicated by cell viability rates of 18.13 % and 20.76 % at concentrations of 20 μM and 5 μM, respectively. This study expands the understanding of E. helioscopia terpenoids’ structural diversity and biological activities, contributing to the exploration of potential therapeutic applications. 相似文献
47.
Xiang-yun Zhu 《Nordic Journal of Botany》2003,23(3):373-384
The pollen morphology of Gueldenstaedtia gansuensis. G. gracilis, G. henryi, G. monophylla. G. mutijlora, G. stenophylla. and G. verna and Tibetia liangshanensis, T. tongolensis, T. yadongensis. T. coelestis, and T yunnanensis are reported for the first time. The seed morphology of G. gracilis, G. maritima. G. monophylla, G. mutiflora, G. taihangensis, and G. verna and L coelestis, T. himalaica, T. yunnanensis, and T. yadongensis are firstly described here. In pollen morphology, the differences of pollen grains of Gueldenstaedtia and Tibetia are as follows: Gueldenstaedtia with pollen grains 3–colporate, psilate, and shapes spheroidal, sometimes subprolate, prolate or oblong; and Tibetia with pollen grains 3– and 4–colporate, perforate, shapes spheroidal, sometimes subprolate or prolate. These results, combined with the data of the basic chromosome number x=7 of Gueldenstaedtia and x=8 of Tibetia, support that the two genera should be recognized as two distinct genera, which are consistent with their morphological characters: Gueldenstaedtia with 2 upper lobes of calyx free, stipules free, adnate to petiole, and Tibetia with 2 upper lobes of calyx connate, stipules connate and opposite to leaves. In Tibetia, two types of pollen grains, 3– and 4–colporate pollen grains, are found. Regarding seed morphology: Gueldenstaedtia has circular depression, irregular circular depression or irregular circular reticulation on the surface; Tibetia has smooth surface. The differences in seed morphology of the two genera also support that they should be kept separate. The pollen morphology supports that G. gansuensis, G. gracilis, G. multiflora, G. stenophylla, and G. verna should be reduced into one species consistent with their morphological characteristics. The pollen grains of G. henryi are different from those of the other species in having wide colpi. 相似文献
48.
Detection of Salmonella typhi by polymerase chain reaction 总被引:1,自引:0,他引:1
A rapid and sensitive method for detection of Salmonella typhi would help in preventing the spread of outbreaks and in clinical diagnosis. In order to develop unique PCR primers to detect Salm. typhi , ribosomal RNA genes from Salm. typhi (Rawlings) were cloned in pUC18. The resulting clone was confirmed by sequencing. The cloned DNA fragment contained the 5S, part of the 23S rRNA genes and the 5S-23S spacer region (EMBL/GenBank accession No. U04734).
It was expected that the 5S-23S spacer region is divergent unlike the highly conserved 23S+5S genes. This was confirmed by comparison with the rRNA gene sequences in the EMBL/GenBank database. A pair of PCR primers specific for Salm. typhi was obtained, based on this spacer region sequence. The specificity of this pair of primers was tested with 54 Salm. typhi strains (of 27 different phage types). All these Salm. typhi strains showed the positive 300 bp PCR product with this pair of primers. Six other Salmonella species as well as six other non- Salmonella bacteria were tested and none showed the 300 bp PCR product. The sensitivity of the detection level was 0·1 pg of pure Salm. typhi genomic DNA, or approximately 40 Salm. typhi cells in a spiked food sample. This pair of primers therefore has the potential for development into a diagnostic tool for the rapid diagnosis of typhoid fever. 相似文献
It was expected that the 5S-23S spacer region is divergent unlike the highly conserved 23S+5S genes. This was confirmed by comparison with the rRNA gene sequences in the EMBL/GenBank database. A pair of PCR primers specific for Salm. typhi was obtained, based on this spacer region sequence. The specificity of this pair of primers was tested with 54 Salm. typhi strains (of 27 different phage types). All these Salm. typhi strains showed the positive 300 bp PCR product with this pair of primers. Six other Salmonella species as well as six other non- Salmonella bacteria were tested and none showed the 300 bp PCR product. The sensitivity of the detection level was 0·1 pg of pure Salm. typhi genomic DNA, or approximately 40 Salm. typhi cells in a spiked food sample. This pair of primers therefore has the potential for development into a diagnostic tool for the rapid diagnosis of typhoid fever. 相似文献
49.
We compared the pattern of 3-phosphorylated phosphoinositides produced by confluent 3T3-L1 preadipose cells upon exposure to growth factors that either induce differentiation (insulin, insulin-like growth factor-1) or do not (platelet-derived growth factor). Following addition of insulin or insulin-like growth factor-1, PI(3,4,5)P3 rapidly rose, on average, to levels tenfold over basal. PI(3,4)P2 either did not change (after insulin) or slightly increased (1.5 fold). Time course studies with insulin demonstrated that the rise in PI(3,4,5)P3 peaked by 1 minute, and levels then remained steady over 30 minutes. Dose-response experiments showed that insulin at a concentration of 1 nM was sufficient for the PI(3,4,5)P3 response. Insulin failed to increase PI(3,4)P2 at any of the time points or at any of the doses used. In contrast, after addition of platelet-derived growth factor, both PI(3,4)P2 and PI(3,4,5)P3 rose concurrently and to comparable extents. These data suggest that one possible mechanism contributing to insulin/insulin-like growth factor-1-induced 3T3-L1 preadipose cell differentiation is a distinct pattern of 3-phosphorylated phosphoinositide accumulation, defined by a prominent increase in PI(3,4,5)P3 with no (in the case of insulin), or a minimal (in the case of IGF-1), rise in PI(3,4)P2. 相似文献
50.