星斑川鲽MHCⅡ恒定链Ii基因的克隆和表达特性

为了研究星斑川鲽MHCⅡ类分子的作用及调控机制,实验通过SMART-RACE技术克隆得到了星斑川鲽MHCⅡ恒定链(MHCⅡIi)的全长cDNA序列,其长度为1766 bp,包含135 bp的5′非编码区、837 bp的开放阅读框和794 bp的3′非编码区。该基因共编码279个氨基酸。理论分子量为30.848 ku,等电点为6.89。与已知物种MHCⅡIi进行同源性比对,结果与狼鲈、紫红笛鲷和鳜关系较近,同源性均为79%。利用quantitative realtime PCR(qRT-PCR)技术检测了MHCⅡIi在星斑川鲽不同组织中的表达,以及爱德华氏菌感染前后对该基因在不同组织中表达水平的影响,结果显示:在脾脏、头肾、肝脏、后肠、性腺、心脏、血液、鳃和肌肉组织中,MHCⅡIi mRNA均有表达,但在表达量上有明显差异,脾脏和头肾组织相对表达水平较高,鳃、血液、肌肉、心脏和性腺中的表达水平较低。病原感染后,免疫相关组织脾脏和头肾的表达水平升高最明显,肝脏和后肠的表达水平也略有升高,但变化不明显。本研究可为星斑川鲽MHCⅡ类分子的作用机理提供理论依据,同时为海水养殖鱼类的抗病遗传育种工作提供研究基础。     

Development and application of fluorescence in situ hybridization (FISH) method for simple and rapid identification of the toxic dinoflagellates Alexandrium tamarense and Alexandrium catenella in cultured and natural seawater

ABSTRACT:   The toxic dinoflagellates Alexandrium tamarense (Lebour) Balech and A. catenella (Whedon and Kofoid) Balech produce potent neurotoxins, such as saxitoxin and gonyautoxin and have been mainly responsible for paralytic shellfish poisoning (PSP) in Japan. To prevent a negative effect on the fishery industry, it is necessary to identify these toxic species precisely and rapidly before and during the bloom. In this paper, a rapid and simple protocol of a fluorescence in situ hybridization (FISH) method using ribosomal RNA (rRNA)-targeted probes has been established for identifying the cultured strains and natural cells of A. tamarense and A. catenella . Using the FISH method established in this study, it was possible to identify these toxic species species-specifically and rapidly, within 30 min. The procedure of detection constituted three steps: (i) fixation/dehydration; (ii) hybridization; and (iii) washing; this made the identification simple. Moreover, this method did not require either special techniques or equipment, and the cost for detection was low. The specificity, rapidity, and simplicity of the developed method suggest that it might be useful for routine monitoring of these toxic microalgae.     

国产人工打洞沉香中一个新的2-(2-苯乙基)色酮二聚体

为进一步研究国产人工打洞法所结沉香中的化学成分,本研究采用硅胶柱色谱、Sephadex LH-20、半制备高效液相等色谱方法从其乙酸乙酯萃取物中分离纯化得到2个单体化合物.根据核磁共振(NMR)、质谱(MS)等波谱数据分别鉴定为2-(2-苯乙基)色酮二聚体(+)-3′,3′′′-dihydroxy-4′,4′′′-di...     

Fucose-Rich Sulfated Polysaccharides from Two Vietnamese Sea Cucumbers Bohadschia argus and Holothuria (Theelothuria) spinifera: Structures and Anticoagulant Activity

Fucosylated chondroitin sulfates (FCSs) FCS-BA and FCS-HS, as well as fucan sulfates (FSs) FS-BA-AT and FS-HS-AT were isolated from the sea cucumbers Bohadschia argus and Holothuria (Theelothuria) spinifera, respectively. Purification of the polysaccharides was carried out by anion-exchange chromatography on DEAE-Sephacel column. Structural characterization of polysaccharides was performed in terms of monosaccharide and sulfate content, as well as using a series of non-destructive NMR spectroscopic methods. Both FCSs were shown to contain a chondroitin core [→3)-β-d-GalNAc-(1→4)-β-d-GlcA-(1→]_n bearing sulfated fucosyl branches at O-3 of every GlcA residue in the chain. These fucosyl residues were different in pattern of sulfation: FCS-BA contained Fuc2S4S, Fuc3S4S and Fuc4S at a ratio of 1:8:2, while FCS-HS contained these residues at a ratio of 2:2:1. Polysaccharides differed also in content of GalNAc4S6S and GalNAc4S units, the ratios being 14:1 for FCS-BA and 4:1 for FCS-HS. Both FCSs demonstrated significant anticoagulant activity in clotting time assay and potentiated inhibition of thrombin, but not of factor Xa. FS-BA-AT was shown to be a regular linear polymer of 4-linked α-L-fucopyranose 3-sulfate, the structure being confirmed by NMR spectra of desulfated polysaccharide. In spite of considerable sulfate content, FS-BA-AT was practically devoid of anticoagulant activity. FS-HS-AT cannot be purified completely from contamination of some FCS. Its structure was tentatively represented as a mixture of chains identical with FS-BA-AT and other chains built up of randomly sulfated alternating 4- and 3-linked α-L-fucopyranose residues.     

基于生态足迹方法的玉米-味精生态农业及产业系统分析

为了提高生态产业研究结果的可比性,以味精产业为例,用生态足迹方法分析了产业过程涉及不同子系统的资源利用和环境污染情况。味精生产由三个子系统构成,玉米生产、淀粉生产和味精生产。计算结果表明,从玉米到味精的生产过程也是生态足迹延长的过程,其中玉米生态足迹占用面积最大,主要是因为耕地和水资源占用大;生态足迹的延长伴随着足迹效益的增加,意味着延长产业链条可以提高资源利用效率;系统的间接能源生态足迹较大,因此应重点考虑降低间接能源的能耗;味精生产系统的能耗最高,空气和水体环境污染最为严重。研究表明,生态足迹是一种很好的衡量复合生态产业不同子系统资源利用和环境污染状况的方法。     

小麦品种对增强UV-B辐射响应的RAPD分析

在前一研究结果的基础上,选用8个对UV-B辐射耐受性不同的小麦品种(4个耐性品种和4个敏感品种),进一步对其进行RAPD分析。结果表明,8个小麦品种间存在着明显的遗传多态性。聚类分析显示,在遗传距离为0.35的水平上,可将它们明显区分出耐性和敏感两大类,这与其生长响应指数(RI)的判定结果基本一致。4个耐性品种共同具有1500bp(OPA-12)的特征谱带,这一分子标记可能与小麦耐UV-B辐射相关,有待进一步研究。     

Pb对匍匐翦股颖根系超氧化物歧化酶活性的影响

通过Pb离子浓度胁迫与处理时间两因素试验方案,利用甲基氮蓝四唑(NBT)光密度测定法测定了匍匐翦股颖(Agrotistolonifera)根系细胞内超氧化物歧化酶(SODs)活性,并用统计分析软件SPSS13.0中的GenearLinearModel模块,对试验数据进行了F测验,用LSD法对各水平间进行多重比较检验。结果表明,重金属Pb各处理浓度对SODs的影响均达到极显著水平,处理后SODs水平显著上升,到第4d时达到最高值,处理第3d与第4d之间未达显著水平,第1、2d与第3、4、5d之间达到极显著水平发现低浓度(<2.5mmol·L-1)Pb处理可促使根系细胞积极的防御策略,使细胞SODs水平持续增加;高浓度(>10.0mmol·L-1)处理使SODs活性在早期上升,第4d后SODs开始下降,其主要原因是Pb离子胁迫产生的超量自由基导致酶失活效应所致。     

高坡猪GH基因不同基因型对其部分生产性能的影响

采用PCR-RFLP-ApaⅠ方法检测高坡猪GH基因-119~ 486 bp片段的多态性,探讨了不同基因型对其部分生产性能的影响。结果表明:产生2个等位基因A(449 bp)和B(316 133 bp),其频率分别为0.54和0.46;3种基因型:AA、AB和BB,其频率分别为0.26、0.56和0.18;除6月龄腹围和背膘厚外,其余指标值均以BB基因型最高,AA基因型的6月龄腹围和瘦肉率与BB基因型相比差异显著(P<0.05),其他指标在各基因型间差异均不显著(P>0.05)。表明,A可能是小型猪的有利等位基因,B则可能是大型猪的有利等位基因。     

石羊河流域玉米棉铃虫发生气象条件分析预测

为深入了解石羊河流域玉米田棉铃虫的发生规律和准确预测其危害特征,以石羊河流域1999～2007年玉米田棉铃虫和气象资料为基础,运用膨化相关、SPSS统计软件进行逐步回归、方差分析,分析、模拟了气象因子与卵始见期、卵高峰持续期、高峰期百穗卵量关系和预测模型,模型回代检验效果较好.结果表明:棉铃虫累计百株卵量增长动态符合典型的"S"生长曲线,Nt=206.8536/1+e3.8130-0.3703t,呈缓慢增长-快速增长-减速增长.棉铃虫卵始见期与光热因子呈负相关,与风、水分因子呈正相关;高峰期百穗卵量与此恰恰相反.热量多、气温高使棉铃虫的繁殖力和生存力提高,棉铃虫卵出现早、年发生程度重.棉铃虫卵期、蛹期相对干旱利于卵的羽化,使卵出现早、卵量增加.     

干巴菌菌丝营养生理特性的初步研究

本文报道了不同碳源、氮源、微量元素及维生素培养基对干巴菌菌丝生长的影响。试验表明,干巴菌菌丝利用最好的的碳源是葡萄糖,其次是蔗糖。利用最好的氮源是硝酸钙,其次是硝酸铵和硫酸铵,对蛋白胨和尿素的利用效果差。缺少碳源或氮源时,菌丝生长细弱、稀少,不形成原基。微量元素和维生素均对干巴菌菌丝生长有促进作用,其中以锰、铜和维生素Ｂ２的作用尤为突出。