利用远缘杂交创造核果类果树新种质的研究

以桃、杏、李、樱桃、杏梅等果树的 1 4个品种为亲本 ,3年来共进行了 80余个组合的远缘杂交试验 ,探讨了核果类果树远缘杂交的亲和性 ,并对远缘杂种幼胚进行了胚抢救。结果表明 ,铃铛花期授粉的坐果率显著高于初花期授粉 ;同一杂交组合 ,正反交坐果率差异显著 ,母本对远缘杂交亲和性影响很大 ,选择自交亲和或自然坐果率高的种或品种做母本容易克服远缘杂交的不亲和性 ;适宜场强的静电场、He -Ne激光处理及60 Coγ射线与He -Ne激光联合处理花粉 ,均能显著提高花粉离体萌芽率 ,用上述处理的花粉进行的远缘杂交坐果率也明显高于对照 ;60 Coγ射线单独处理则降低了花粉离体萌芽率 ,远缘杂交的坐果率也低于对照 ;对远缘杂种幼胚及时地进行胚抢救 ,并诱导形成多丛芽 ,是克服核果类果树远缘杂种不育性的有效方法。研究并筛选出了李、樱桃胚萌发与生长、多丛芽诱导与增殖以及生根培养等最佳培养基配方。目前已将欧洲甜樱桃×中国樱桃、大石早生李×泰安巴旦水杏及凯特杏×总统李等一批核果类果树远缘杂种定植于露地 ,其中欧洲甜樱桃与中国樱桃的种间杂种是国内外首次获得     

单性结实与自花结实柑橘果实发育中钙钾动态的研究

 对单性结实的‘国庆1 号’温州蜜柑和自花结实的‘华农本地早’橘从开花前子房发育至果实成熟采收期整个子房或幼果及果实的不同部位(果皮和果肉) 的钙与钾含量变化进行了测定。结果表明:1) ‘国庆1 号’花前及花期子房钙含量较高, 花后趋降; 而其钾含量在花前及花期相对较低, 花后上升;2) ‘华农本地早’花前子房钙含量相对较低, 花后有一上升过程; 而对应钾在花前及花期就已很高, 花后下降; 3) 两品种果肉的钙含量自花后65 d 后均呈下降趋势, 而‘国庆1 号’果皮的钙含量在花后80 d 有一显著上升, 对应的‘华农本地早’在花后125 d 才急剧增加, 之后直至果实成熟二者均维持在较高水平;4) 两品种果皮、果肉的钾含量在果实发育过程中均呈类似的下降趋势。     

冰核细菌对仁用杏胚珠超微结构的影响

 应用透射电镜对两个仁用杏品种‘白玉扁’和‘一窝蜂’接种冰核细菌并低温处理后的胚珠超微结构进行了观察, 发现冰核细菌对胚珠的超微结构有一定影响: (1) 使珠心细胞发生严重的质壁分离,细胞质中存在大量泡状结构, 线粒体的内部结构完全被破坏, 呈透明状, 而且有些珠心细胞中形成同心圆状的多膜内含物; (2) 使胚囊中卵细胞的细胞核外膜膨胀, 甚至核膜局部解体, 细胞质中细胞器减少。这些变化致使胚珠发育不正常, 影响受精而导致减产或绝收。接种冰核细菌并低温处理比单纯低温处理对胚珠超微结构的破坏程度重。     

草莓摘叶处理对果实芳香物质的影响

 对草莓(Fragaria×ananassa Duch．)‘哈达’品种坐果后植株进行摘叶处理，对成熟果实的糖类和芳香物质含量进行了测定分析，结果表明：不摘叶、摘1/3叶和摘2/3叶3个处理果实GC/MS分析分别检测出43、33和37种芳香物质成分。随摘叶程度加重，芳香物质成分中酯类的相对含量呈下降趋势，而醛类的相对含量呈上升的趋势；2，5-二甲基-4-甲氧基-3(2H)-呋喃酮的相对含量明显降低；果糖和总糖含量显著降低。     

我国椪柑品质现状及主要产区的果实品质比较

 2001 和2002 年对来自全国9 个省(市) 主要产区的67 份椪柑品质进行了分析。结果表明, 我国椪柑大(180.60 g ±9.98 g) 、中(151.24 g ±7.48 g) 、小(122.51 g ±141.1 g) 类型果实分别为42.9 %,44.9 %和12.2 %; 分别有6.1 %和44.9 %的　柑果皮颜色呈现黄绿或偏黄色和黄色; 可溶性固形物平均含量为12.5 %±1.1 %, 其中仅有四川荣县、福建平和和湖北松滋等部分地区　柑可溶性固形物含量低于11.5 %;高酸(0.95 % ±0.10 %) 、中酸(0.69 % ±0.07 %) 和低酸(0.49 % ±0.07 %) 类型的果实比例分别为2.4 %、34.7 %和42.9 %。通过比较各椪柑主产区的主要品质指标发现, 它们的果皮色泽(a/ b 比值) 、可溶性固形物含量和维生素C 含量没有明显差异; 闽中南地区的果实明显重于闽北、浙江(衢州、丽水) 和湘西鄂西地区的果实, 而与川西南地区的差异不明显; 闽中南地区和川西南地区的酸含量差异不明显, 但都明显低于另两个地区; 另外, 川西南地的区固酸比明显高于其他3 个地区, 而可食率明显低于其他3 个地区。     

三尖杉枝叶粉末防治花生根结线虫病

采用盆栽及大田小区试验,研究了三尖杉Cephalotaxus fortunei枝叶干粉末对花生根结线虫病的防治效果.盆栽试验结果表明,每盆(2kg土)施用三尖杉枝叶干粉末10、15及20 g三种处理,与对照组相比,初侵染相应推迟4、6、10天,并能减少侵染量,降低根结增长率,显著减轻花生根结线虫病病情.大田小区试验结果与盆栽试验结果相似,每小区(5m2)沟施三尖杉枝叶干粉末120、80、50 g,处理后34及53天的2次平均防治效果分别为89%、82%及50%,施药对照10%益舒宝颗粒剂25g处理(相当于45kg/hm2)为74%.综合使用剂量及花生生长情况,建议沟施150kg/hm2三尖杉枝叶干粉为宜.     

额济纳旗浅层地下水环境研究

通过 2 0 0 3年 4- 5月在黑河下游额济纳分两条路线 (a -a’和b -b’)采集水样 ,分析了额济纳现状水资源特征。远离河道区域水化学类型有HCO3·SO4-Na、Cl·SO4-Na·Ca、HCO3·Cl-Na·Ca和SO4·Cl-Na ;在河道附近或河道地区水化学类型主要是SO4·HCO3-Na ,类型单一 ;研究区矿化度和各离子含量随距离补给源的远近增减而升降 ,表明它们主要依赖于上游补给水量 ;同时 ,额济纳地处干旱区 ,降雨稀少 ,该区植被的生长发育主要依靠浅层地下水 ,地下水环境的改变直接导致了区域生态的变化。     

Effect of EGFP gene transfection on the cell cycle distribution of primary cultured human chondrocytes

AIM: To investigate the effect of enhanced green fluorescence protein (EGFP) gene transfection on the cell cycle distribution of primary cultured human chondrocytes in order to establish a tracking method of cultured human nasoseptal chondrocytes. METHODS: pEGFP-N1 plasmid was amplified in E.coli, and purified by high purity kit. Primary cultured human chondrocytes,which were initially obtained from the nasoseptal cartilage, were cultured in vitro and transferred with pEGFP-N1 by means of electroporation with Amaxa nucleofector device. Transfering process and transient expression were evaluated by laser scanning confocal microscope (LSCM), the transfer efficiency and the cell cycle distribution were evaluated by flow cytometry. RESULTS: There was significant expression of EGFP at 24 h after transferring. The transfection efficiency of pEGFP-N1 into primary cultured human chondrocytes reached 35.37％ at 48 h. It didn't affect the process of cell adherance and had no effect on the cell cycle distribution. CONCLUSION: Primary cultured human chondrocytes, which were transfected with pEGFP, are alive in vitro, and the transferring process doesn't affect the cell cycle distribution. These results suggest that pEGFP-N1 is an ideal transient expression vector for primary cultured human chondrocytes and it might be a well tracer in construction tissue engineered cartilage.     

The ex vivo expansion characteristic of endothelial progenitor cells

AIM: To explore the ex vivo expansion characteristics of the endothelial progenitor cells (EPCs). METHODS: CD34⁺ cells were selected from umbilical cord blood mononuclear cells (MNC) by MiniMACS system, expanded at the same conditions as that for total MNC, coincubation of CD34⁺ and CD34^- from the same donation for EPCs. In addition, we tested the effect of vessel endothelial growth factor (VEGF) and passage on cell differentiation, expansion kinetics and apoptosis. EPCs were determined and quantified by immunocytochemistry and flow cytometry. RESULTS: Coculture of CD34⁺ and CD34^-,total MNC led to a significant increase in the expansion of CD34⁺ cells compared with CD34 enrichment (P＜0.05). There was a trend toward decreased apoptosis in cultures when early passage was performed once the linear cord like structures appeared. There was no significant effect on apoptosis between with VEGF and without VEGF group (P＞0.05). These differentiated EPCs were stained positive for CD34⁺, von Willebrand factor (vWF), KDR, CD31 and incorporate acetylated low-density lipoprotein (LDL). CD34⁺ and AC133⁺cells accounted for 68.2%±6.3% (n=6) and 57.2%±9.8% (n=6) of attaching (AT) cells at day 7 of culture, respectively. CONCLUSIONS: Coculture of CD34⁺ and CD34^- or culture of MNC enhances ex vivo expansion of EPCs. Early passage decreases apoptosis rate, VEGF has no significant effect on ex vivo expansion of EPCs.     

Radioligand binding assay of insulin receptor in rabbit kidney during ischemic and reperfusion

AIM: To observe the change of insulin receptor in rabbit kidney with acute ischemic-reperfusion injury. METHODS: 15 Japanese white rabbits were allocated randomly into control group, ischemic-reperfusion group(IR group). IR group received clamping for 1 h followed by 2 h or 48 h of reperfusion. At 2 h or 48 h after reperfusion, glucose and insulin in serum were determined. Insulin receptor in renal tissue was analyzed by radioligand binging assay(BAD). RESULTS: The level of serum glucose increased after 2 h reperfusion in 2 groups, but in IR group the value increased much more higher than those in control groups(P＜0.05). Plasma insulin of IR group was significantly higher than that in control after 2 h reperfusion(P＜0.05). Scatchard analysis of data resulted in curvilinear profiles, indicating that there are two classes of receptors with different affinity or the presence of a single class of receptors with a negative cooperative hormone-receptor interaction. Data analyzed for a two-site model showed that the values of Bmax₁(high affinity site), Bmax₂(low affinity site) and Kd₁, Kd₂ were significantly lower than that of control (P＜0.05) after 2 h perfusion. 48 h after IR there was no difference of Bmax₁, Bmax₂, and Kd₁ between 2 groups,but Kd₂ of IR group was higher than that of control (P＜0.05). CONCLUSIONS: The results indicate that the effect of intrinsic insulin decreases in the progress of the renal ischemic-reperfusion. The resulting high serum glucose may aggravate renal injury in the progress of ischemic-reperfusion.