黄瓜低温弱光耐受性机理及其应用研究的主要进展

选择低温弱光抗性水平不同的欧洲温室型、欧亚杂交型、华北温室型、华北露地型黄瓜(Cucumis sati- vus L.)的16个品种为试验材料,以光合代谢为切入点,开展苗期光合速率、光补偿点、1,5-二磷酸核酮糖羧化酶 (rubisco)活性和叶绿素a荧光动力学曲线的系统研究,结果表明:单一偏低温和偏低温弱光协效应未明显伤害光合系统,而临界低温可能伤及PSⅡ;偏低温和弱光组合时,弱光对黄瓜幼苗的影响起主导作用,弱光与临界低温组合时,临界低温起主导作用;偏低温弱光(单一弱光)下的叶面积增长量和临界低温下的冷害指数可分别作为评价黄瓜对偏低温弱光(单一弱光)耐受性和临界低温耐受性的比较稳定可靠的指标,据此设计了相关的评价指标体系。用117个重组自交系为材料,以弱光下叶面积增长量为指标进行弱光耐受性评价并以RAPD、AFLP、SSR分子图谱为基础,通过区间作图,检测到5个与黄瓜弱光耐受性有关的QTLs。采用mRNA差异显示银染技术克隆得到黄瓜冷敏型品种津研4号低温锻炼中特异表达基因的cDNA克隆(ccr18),其大小为639 bp。在基因组中以单拷贝或低拷贝形式存在。序列同源性比较表明它与拟南芥[Arabidopsis thaliana(L．)Heynh．]染色体ⅣBAC库中的 F14P3基因组序列具有88％的同源性。     

西葫芦新品种济葫2号的选育

济葫2号是以QL0133和QLO119配制而成的西葫芦一代杂交种,植株生长旺盛、株型紧凑、矮蔓、早熟、丰产,抗病毒病、白粉病、蔓枯病.瓜浅绿色,嫩瓜长20.0 cm,粗6.0 cm,粗细均匀、品质佳.每667 m2产量达6 500kg,适于早春茬、秋冬茬及越冬茬栽培.     

优质晚熟桃新品种‘美帅’

 ‘美帅’是‘大久保’和‘90-1’ (‘八月脆’ ב京玉’) 杂交育成的优质晚熟桃新品种。果实圆形, 平均单果质量275 g, 果面60% ～80%着鲜红色, 外观美丽。可溶性固形物含量12.6%。风味甜, 鲜食品质佳。果实8月中旬成熟, 丰产性强。     

罗汉果生产技术研究的思路与发展对策

探讨了罗汉果生产技术研究思路，提出选育、引进优良品种，培育茎尖脱毒壮苗，建立种薯基地，采用容器无土栽培、平地栽培、设施栽培，施用天敌真菌、接种VA菌根真菌防治根结线虫等技术建议。     

用外翻肠囊法研究高钙条件下有机锰在肉仔鸡小肠中的吸收特点

本试验用外翻肠囊法研究高钙对肉仔鸡不同肠段(十二指肠、空肠和回肠)吸收不同形态锰的影响,以比较有机锰和无机锰在高钙条件下吸收特点的差异。采用单因子完全随机设计,培养液中添加的4种锰源分别为:硫酸锰、弱络合强度的蛋氨酸锰(Mn-MetE)、中等络合强度的氨基酸锰(Mn-AAA)和强络合强度的氨基酸锰(Mn-AAB)。为了扣除内源的影响,设置1个零添加锰水平处理。将40只31日龄AA肉公鸡随机分到以上5个组,每组8个重复,每个重复1只鸡,每只鸡的十二指肠、空肠和回肠分别作为相应肠段外翻肠囊的一个重复。结果表明:1)体外培养回肠肠囊对锰的吸收率显著高于十二指肠(P<0.01);2)回肠肠囊对强络合强度的Mn-AAB中锰的吸收率显著高于硫酸锰或中等络合强度的Mn-AAA(P<0.05)。本试验结果表明:在高钙条件下,络合形态的有机锰在体外培养的肉仔鸡肠囊中的吸收率显著高于无机形态的锰;强络合强度有机锰源中的锰能更强地抵抗小肠内的解离,比弱或中等络合强度的有机锰源更有利于锰的吸收。     

HPLC法检测发酵玉米粉中的黄曲霉毒素B1、B2、G1、G2

发酵玉米粉用甲醇∶水(80∶20,V∶V)提取黄曲霉毒素(AFT),经免疫亲合柱(IAC)分离纯化、在线光化学衍生器柱后衍生化后,反相高效液相色谱(HPLC)荧光检测器测定AFT(B1、B2、G1、G2)含量。4种毒素在0.5ng/g和2ng/g2个水平下,样品加标回收率平均值分别为B188.0%和93.6%、B285.2%和85.3%、G192.4%和91.5%、G289.6%和85.6%;5次测定的标准差分别为:B12.5和6.3、B23.5和6.0、G12.8和9.0、G22.3和6.9;4种毒素的方法检出限均达到0.05ng/g。     

Culture of Differentiated Adult Rabbit Auricular Chondrocytes

Chondrocytes dedifferentiate to a fibroblast‐like phenotype on plastic surfaces. Dedifferentiation is reversible if these cells are then cultured embedded in gels as alginate, agarose or collagen. Chondrocytes cultured in suspension on a non‐adherent surface are also known to form aggregates of differentiated cells. The knowledge of chondrocyte behavior in culture is relevant for tissue engineering purposes. In this report we describe a simple method to culture differentiated or redifferentiated rabbit auricular chondrocytes on plastic surfaces with a stable phenotype. When chondrocyte aggregates formed in suspension are next seeded on plastic surfaces, most of them attach to the plastic as round or polygonal cells, and this morphological differentiation, confirmed by the presence of type II collagen, is stable for long culture periods. We also report that the addition of aggregates to monolayer cultures of dedifferentiated chondrocytes results in their redifferentiation, as is shown by their morphological changes and the synthesis of type II collagen. Therefore, this simple method can be useful for the study of chondrocyte behavior on plastic surfaces and for redifferentiating previously proliferated chondrocytes in tissue engineering techniques. Furthermore, these results demonstrate that, in addition to culture conditions such as cell isolation method or cell‐density, chondrocyte behavior on plastic depends on the presence or absence of aggregates resulting from the dissociation process.     

辣椒新品种镇江3号的选育

中晚熟杂交一代辣椒镇研3号是以江苏本地羊角椒自交系Y9007为母本,由甘肃酒泉引进的甜椒自交系T9218为父本配制的一代杂交组合。镇研3号为中熟辣椒品种,果形为牛角形,纵径15cm,肩横径5.0cm、肉厚0.40cm,单果平均重42g。果面光滑,青熟果绿色、味微辣,风味佳,适宜在长江流域或南方保护地栽培种植,667m2产量约为4200～5000kg。     

珍黄88(湘椒29号)辣椒的选育

珍黄88的母本6427是从广西地方品种经自交纯化而成的优良黄皮尖椒自交系;父本8215为叶少、部分茎节短缩、肉厚疏松的辣椒高代自交系。该品种中熟,定植至采收青椒约50 d(天),产量2500～2800 kg·(667 m~2)~(-1),抗病毒病,中抗疫病,适于山东、广东等黄皮尖椒外运基地栽培;果实长牛角形,果表黄绿无皱,果型直,肉厚腔小,商品性好,耐贮运。     

Analysis of gene expression profile of multidrug resistant MCF/DOX cell line after benflumetol derivative LY980503 treatment

AIM:To investigate the effect of LY980503(a benflumetol derivative)on multidrug resistance of tumor cell line using DNA microarray.METHODS:Total RNA was extracted from multidrug resistant MCF/DOX cell line. cDNA microarray containing 320 cDNAs was used to detect the gene expression profile.RESULTS:9 down-regulated genes and 1 up-regulated gene were identified after multidrug resistant MCF/DOX cells were treated with LY980503.CONCLUSION:LY980503 can effectively reverse the resistance of MCF/DOX to DOX in vitro by adjusting the expression of multi-genes.