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31.
三褶脉紫菀中的新二萜甙 总被引:1,自引:0,他引:1
三褶脉紫菀(AsterageratoidesTurcz.)系菊科多年生草本植物,遍布全国,是民间常用的中药,有清热解毒、祛痰镇咳的功效[1,2]。化学工作者们曾从其同属植物紫菀(AstertararicusL.f.)中分离到紫菀酮(shionone)、槲皮素(quercetin)、无羁萜(friedelin)、表无羁萜(epifriedelinel)、毛叶醇(lachnophyllol)、乙酸毛叶酯(lachnophyllolacetate)、茴香醚(anethole)以及紫菀三萜皂甙[2—4]… 相似文献
32.
CSE1 and CSE2, two new genes required for accurate mitotic chromosome segregation in Saccharomyces cerevisiae. 总被引:18,自引:2,他引:16 下载免费PDF全文
Z Xiao J T McGrew A J Schroeder M Fitzgerald-Hayes 《Molecular and cellular biology》1993,13(8):4691-4702
By monitoring the mitotic transmission of a marked chromosome bearing a defective centromere, we have identified conditional alleles of two genes involved in chromosome segregation (cse). Mutations in CSE1 and CSE2 have a greater effect on the segregation of chromosomes carrying mutant centromeres than on the segregation of chromosomes with wild-type centromeres. In addition, the cse mutations cause predominantly nondisjunction rather than loss events but do not cause a detectable increase in mitotic recombination. At the restrictive temperature, cse1 and cse2 mutants accumulate large-budded cells, with a significant fraction exhibiting aberrant binucleate morphologies. We cloned the CSE1 and CSE2 genes by complementation of the cold-sensitive phenotypes. Physical and genetic mapping data indicate that CSE1 is linked to HAP2 on the left arm of chromosome VII and CSE2 is adjacent to PRP2 on chromosome XIV. CSE1 is essential and encodes a novel 109-kDa protein. CSE2 encodes a 17-kDa protein with a putative basic-region leucine zipper motif. Disruption of CSE2 causes chromosome missegregation, conditional lethality, and slow growth at the permissive temperature. 相似文献
33.
半乳甘露聚糖植物胶加工是我国70年代中期兴起的新兴产业。本文从我国植物资源发展的角度。重点论证了瓜尔豆(Cyanopsis tetragonoloba(L.)Taubert.)、田菁(Sesbania cannabina(Retz.)Pers.)、胡芦巴(Trigonella foenum-graecum L.)的生产情况,认为胡芦巴适应性强、产量高、易于机械化大面积种植与轮作,并具有改良土壤以及经济效益好等优势。因此,发展半乳甘露聚糖胶资源,大量种植胡芦巴是最好的选择。 相似文献
34.
35.
Rukui Zhu Yu Liang Huajian Luo Huishan Cao Yi Liu Shan Huang Qi Xiao 《Journal of molecular recognition : JMR》2023,36(1):e3000
In this work, binding interactions of artemisinin (ART) and dihydroartemisinin (DHA) with human serum albumin (HSA) and bovine serum albumin (BSA) were investigated thoroughly to illustrate the conformational variation of serum albumin. Experimental results indicated that ART and DHA bound strongly with the site I of serum albumins via hydrogen bond (H-bond) and van der Waals force and subsequently statically quenched the intrinsic fluorescence of serum albumins through concentration-dependent manner. The quenching abilities of two drugs on the intrinsic fluorescence of HSA were much higher than the quenching abilities of two drugs on the intrinsic fluorescence of BSA. Both ART and DHA, especially DHA, caused the conformational variation of serum albumins and reduced the α-helix structure content of serum albumins. DHA with hydrophilic hydroxyl group bound with HSA more strongly, suggesting the important roles of the chemical polarity and the hydrophilicity during the binding interactions of two drugs with serum albumins. These results reveal the molecular understanding of binding interactions between ART derivatives and serum albumins, providing vital information for the future application of ART derivatives in biological and clinical areas. 相似文献
36.
37.
A system for somatic embryogenesis and plant regeneration of spinach from hypocotyl segments has been established. Callus
was induced on solid media supplemented with 8.5–15.0 mg.l−1 of indole-3-acetic acid and 3.46–34.64 mg.l−1 gibberellic acid. Callus was then subcultured on different media (solid or liquid) with or without IAA, or continuously maintained
on the initiating media. Somatic embryos were obtained in subcultures on IAA-containing media as well as in long-term cultures
on initiating media. The best results were achieved in liquid subcultures. About 60% of plantlets survived after transplanting
in pots. 相似文献
38.
Yung-Chieh Tsai Tian-Ni Kuo Yu-Ying Chao Pei-Rong Lee Ruei-Ci Lin Xiao-Yi Xiao Bu-Miin Huang Chia-Yih Wang 《Journal of cellular biochemistry》2023,124(1):89-102
Testes control the development of male reproductive system. The testicular interstitial Leydig cells (Leydig cells) synthesize testosterone for promoting spermatogenesis and secondary sexual characteristics. Type A platelet-derived growth factor (PDGF-AA) is one of the most important growth factors in regulating Leydig cell growth and function. Knockout of PDGF-AA or its congenital receptor PDGFR-α leads to poor testicular development caused by reducing Leydig cell numbers, supporting PDGF-AA/PDGFR-α signaling regulates Leydig cell development. Primary cilium is a cellular antenna that functions as an integrative platform to transduce extracellular signaling for proper development and differentiation. Several receptors including PDGFR-α are observed on primary cilia for initiating signaling cascades in distinct cell types. Here we showed that PDGF-AA/PDGFR-α signaling promoted Leydig cells growth, migration, and invasion via primary cilia. Upon PDGF-AA treatment, AKT and ERK signaling were activated to regulate these cellular events. Interestingly, active AKT and ERK were detected around the base of primary cilia. Depletion of ciliary genes (IFT88 and CEP164) alleviated PDGF-AA-activated AKT and ERK, thus reducing Leydig cell growth, migration, and invasion. Thus, our study not only reveals the function of PDGF-AA/PDGFR-α signaling in maintaining testicular physiology but also uncovers the role of primary cilium and downstream signaling in regulating Leydig cell development. 相似文献
39.
为研究鲸类低氧适应的分子机制,文章克隆了不同低氧耐受能力的3个鲸类物种,抹香鲸(Physeter macrocephalus)、白鲸(Delphinapterus leucas)和长江江豚(Neophocaena phocaenoids asiaeorientalis)的脯氨酸羟化酶2(PHD2)。通过对其序列进行分析,发现3个物种PHD2的氨基酸序列非常保守。通过对这3个物种的PHD2的功能进行探究发现:3个物种的PHD2在常氧情况下均可以降解3个物种的HIF-α(包括HIF-1α和HIF-2α)蛋白,而在低氧(O2浓度小于2%)情况下,PHD2则无法明显降解HIF-α蛋白。在常氧下,鲸类的PHD2降解HIF-α是依赖于识别鲸类的HIF-1α上LTLLAP和LEMLAP,HIF-2α的LAQLAP和LETLAP氨基酸片段,推测PHD2是通过对HIF-α序列中的脯氨酸位点进行羟基化修饰后,被VHL-E3泛素连接酶复合体所识别,发生泛素化降解。而在低氧条件下,PHD2的活性受到抑制HIF-α不能被VHL-E3泛素连接酶复合体识别,发生降解。研究对3种不同低氧耐受能力... 相似文献
40.
To develop new highly effective anticancer agents derived from naturally occurring stilbene scaffold, in total of 24 indole and indazole-based stilbenes including 17 new compounds were designed according to molecular hybridization strategy and synthesized via Witting reaction. The cytotoxic screening results against human tumor cell lines (K562 cells and MDA-MB-231 cells) showed that indole and indazole-based stilbenes are of great interest for developing anticancer agents as eight derivatives possessed strong antiproliferative activities with IC50 values less than 10 μM, and those synthetic derivatives displayed more higher cytotoxicities against K562 cells than MDA-MB-231 cells. In particular, indole-based stilbene bearing piperidine exhibited the most potent cytotoxicities against both K562 and MDA-MB-231 cells with IC50 values 2.4 μM and 2.18 μM, respectively, along with a remarkable selectivity towards human normal L-02 cells. Together, the results suggested that indole and indazole-based stilbenes are promising anticancer scaffolds worthy of further investigation. 相似文献