青阳参的大孢子发生与雌配子体发育

利用常规石蜡制片技术、荧光显微技术、光镜细胞化学技术、电子显微镜技术对青阳参大孢子发生、雌配子体形成过程进行了详细观察。结果显示,青阳参为边缘胎座,胚珠倒生、短珠柄,单珠被,薄珠心型,珠心细胞含有大量的淀粉粒、线粒体和内质网等;大孢子孢原细胞起源于下表皮并直接行使大孢子母细胞的功能;合点端的大孢子分裂形成8-核胚囊;蓼型胚囊;成熟胚囊中有大量淀粉粒;珠孔受精;胚乳在早期发育阶段以游离核形式存在,约在16~32核的阶段细胞壁形成,通常情况下胚乳核的分裂比合子的分裂早,成熟胚乳细胞单核、形状不规则,没有胚乳吸器;胚的发育经过原胚、球型胚和心型胚阶段,茄型;成熟的种子具有种毛,位于珠孔端的珠被表皮细胞是种毛长出的区域,种子中含有大量的脂肪。     

MSI2通过下调circRNA_001214促进急性髓系白血病细胞HL60生长

Musashi-2（MSI2）是一种RNA结合蛋白质,对维持造血干细胞功能具有重要作用。研究表明,MSI2高表达能促进急性髓系白血病（acute myelocytic leukemia, AML）进展,但其作用机制尚不明确。本研究稳定沉默HL60细胞MSI2后,第1、2、3、4 d对照组的相对细胞生长率分别为1.931 ± 0.027、3.070 ± 0.073、4.017 ± 0.092和4.215 ± 0.246;敲减组分别为1.927 ± 0.035、2.564 ± 0.090、2.825 ± 0.097和3.223 ± 0.182,两组相比具有统计学差异,P<0.001;细胞凋亡明显增加(7.967% ± 0.698% vs 3.400% ± 0.322%., P<0.01);G₀/G₁期细胞比例明显增高（67.430% ± 4.390% vs. 50.360% ± 2.160%, P<0.01）;NUMB蛋白明显上调,LEF1明显下降。环状RNA（circular RNA, circRNA）芯片筛选和荧光定量PCR验证显示,MSI2沉默组circRNA_001214表达水平是对照组3.48倍。这一结果也在NALM6细胞得到证实。进一步用生物信息学分析,显示circRNA_001214最可能与miR-1273a、miR-1273e和miR 5095结合,进而影响参与细胞凋亡相关基因（CYCS、AKT1、BAX、TNFRSF10A、TNFRSF10D）、Wnt信号基因（WNT4、WNT2B、WNT7B、 DKK2、SFRP1、CSNKE1和LEF1）以及参与细胞代谢相关基因（RPE, PGAM4, PGAM1, TAT, CBS、RPE、SUCLG2、PGAM4、PGAM1和 IDNK）。总而言之,MSI2可能通过干扰circRNA_001214生成,减少靶miRNA对凋亡、Wnt信号及细胞代谢相关基因表达的影响,促进细胞生长。     

陆地棉栽培品种转复合启动子控制下的cry 1Ac3基因获得高效抗虫植株

以根癌土壤杆菌( Agrobacterium tumefaciens )介导法分别将植物表达载体pBinMoBc和pBinoBc导入陆地棉( Gossypium hirsutum L.)栽培品种"新陆早1号"、"晋棉7号"、"晋棉12号"和"冀合321".pBinMoBc携带有高效启动子复合OM启动子控制下的 cry 1Ac3基因,pBinoBc携带有35S启动子控制下的 cry 1Ac3基因.经过共培养、卡那霉素筛选抗性愈伤组织及体细胞胚的诱导,得到了再生植株.对T2代的PCR、Southern blotting、ELISA检测及Western blotting证明 cry 1Ac3基因已整合入受体棉花基因组并得到表达.抗虫性检测表明转基因后代对棉铃虫( Heliothis armigera ) 具有良好的抗性,转pBinMoBc T2代与转pBinoBc T2代相比,对棉铃虫具有更快的致死速度.本研究建立了一套高效的陆地棉栽培品种转化体系;进一步的检测结果表明,复合OM启动子可以提高外源基因的表达量从而增强转基因棉的抗虫性.     

山东海岸木生海洋真菌的研究I.(英文)

为调查中国黄海海域的丝状海洋真菌,从山东威海潮间带海滩收集了沉没木、附着木和沙埋木,并从其上分离到7种高等海洋真菌。Arenariomycestrifurcata,Corollosporamaritima,Alternariamaritima,Trichocladiumachrasporum为中国大陆新记录种,Chaetomiunglobosum,Tetraploaaristata,Torulasp.为中国大陆新生境报道。对每个种作了描述并对分类和形态进行了讨论。     

不同培养基质对草菇营养成分及呈味物质的影响

在栽培条件一致的情况下,以5种不同培养基质栽培的草菇子实体为研究对象,测定粗蛋白、水解氨基酸、游离氨基酸、可溶性糖醇、有机酸及5′-核苷酸组成与含量,研究不同培养基质对草菇子实体营养成分及呈味物质的影响。结果表明以棉籽壳为基质栽培草菇,其粗蛋白及水解氨基酸含量及组成最优;以稻草为基质栽培草菇,其可溶性糖醇、有机酸含量最高。综合各种呈鲜成分,等鲜浓度值（equivalent umami concentration,EUC）范围为317.45-708.75g MSG/100g,其中以棉籽壳为基质栽培的草菇子实体EUC值最高,以刺芹侧耳菌渣为基质栽培的草菇EUC次之,以金针菇菌渣为基质栽培的草菇EUC [(317.45±13.67)g MSG/100g]最低,约为棉籽壳样品EUC值的44.79%。因此,培养基质对草菇呈味物质的影响显著,可根据需要的呈味物质选用不同的培养基质栽培草菇。     

华山新麦草开花物候期观测和自然种群基因流的间接估测

华山新麦草（Psathyrostachys huashanica keng)为我国特有种,仅分布在陕西华山。通过对自然种群传粉物候期观测发现,华山新麦草的传粉高峰期与海拔有一定关系。海拔每升高200m,传粉物候期就推迟2－3d;海拔差异超过500m的亚种群,传粉物候期就不会出现重叠。同时应用等位酶分析技术和E－统计分析间接估测华山新麦草自然种群的基因流（Nm）,其值较一般风媒传粉植物低。通过华山新麦草资源状况、生长环境的调查以及移栽试验的观察,认为该物种稀的主要原因之一 可能是其生存竞争能力弱,最终被迫生长在其它物种所不能生存的环境。     

Pharmacokinetics and metabolism of 3,4-dichlorophenyl-propenoyl-sec.-butylamine in rats by high performance liquid chromatography-ion trap mass spectrometry

The pharmacokinetics (PK) and metabolism of 3,4-dichlorophenyl-propenoyl-sec.-butylamine (3,4-DCPB), a novel antiepileptic drug, were investigated after its oral administration to rats (100 mg/kg) by HPLC. The absorption and elimination of 3,4-DCPB were rapid. 3,4-DCPB was found to undergo extensive metabolism as the major route of elimination. Structures of the metabolites present in rat plasma were identified with liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS/MS). It was concluded that 3,4-DCPB was involved in the multiple metabolic pathways (hydrolysis, dealkylation and oxidation) and the hydrolysis product, 3,4-dichloro-cinnamic acid (M1) appeared to be the major metabolite.     

居群遗传学原理及其在珍稀濒危植物保护中的应用

居群遗传学在珍稀濒危植物保护研究中有着重要的应用价值。本文首先介绍了居群遗传学中的几个重要概念——有效居群大小、近交繁殖、遗传漂变和基因流,然后详细叙述了居群遗传学原理在珍稀濒危植物保护中的应用途径和前景。     

转基因烟草中Bt毒蛋白基因的表达行为

Bt toxin genes were the insecticidal genes most widely used in genetic engineering of pest resistant plant, were of important significance to study their expression behavior in transgenic plants. In this work, a plant expression vector, pBinMoBc, was constructed. It contained the Cry IA(c) gene under control of chimeric OM promoter and the Ω factor. The vector was transferred into tobacco (Nicotiana tabacum L.) plant via Agrobacterium-mediated transformation. ELISA assay showed that the expression levels of the Cry IA(c) gene in transgenic tobacco plants were significantly higher than that in wild-type tobacco plants. The highest could be up to 0.255% of total soluble proteins; the expression level of CryIA(c) gene in transgenic tobacco plant was changeable during the development stages of tobacco plant. Bioassay showed that pBinMoBc transgenic tobacco plants had more notable insecticidal activity than the wild-type tobacco plants. The above results indicated that pBinMoBc was an effective pest-resistent plant expression vector. This study would be very helpful in screening transgenic cotton with high resistance to cotton bollworm (Heliothis armigeva Hubner).