植物的抗螨机理

植食性螨类分布广泛,危害多种寄主植物.本文从3个方面介绍了植物的抗螨机理:植物形态如叶型、叶色主要影响螨类的取食产卵位点和营养物质的获取;植物组织结构如叶厚、蜡质、茸毛、气孔等决定螨能否顺利利用口针取食到植物的汁液,而虫菌穴则作用于捕食螨和植食性螨的相互关系,从而达到保护植物的目的;植物理化性质如叶鲜重、生长速度、生育...     

玉/豆和玉/薯模式下氮肥运筹对玉米氮素利用和土壤硝态氮残留的影响

过量施用氮肥造成的环境问题日益严重,氮肥合理使用已成为人们研究的热点.本文研究了西南玉米两种主要套作模式下氮肥运筹对玉米氮素利用和土壤硝态氮残留的影响.结果表明：连续分带轮作种植玉/豆模式后,玉米收获期植株中的氮素积累较玉/薯模式平均提高了6.1%,氮收获指数增加了5.4%,最终使氮肥利用效率提高4.3%,氮素同化量提高了15.1%,氮肥偏生产力提高了22.6%;玉米收获后硝态氮淋溶损失减少,60～120 cm土层中硝态氮残留玉/豆模式较玉/薯模式降低了10.3%,而0～60 cm土层中平均提高了12.9%,有利于培肥地力,两年产量平均较玉/薯模式高1249 kg·hm^-2,增产22%;增加施氮量提高了植株氮素积累,降低了氮肥利用率,显著提高了表层土壤中硝态氮的累积,60～100 cm土层中硝态氮的累积量在0～270 kg·hm^-2处理间差异不显著,继续增加施氮量会显著增加土壤硝态氮的淋溶;氮肥后移显著提高了土壤0～60 cm土层硝态氮的积累.两种模式下施氮量和底追比对玉米氮素吸收和硝态氮残留的影响结果不一致,玉/豆模式以施氮180～270 kg·hm^-2、按底肥∶拔节肥∶穗肥=3∶2∶5的施肥方式有利于提高玉米植株后期氮素积累、氮收获指数和氮肥利用效率,减少了氮肥损失,两年最高产量平均可达7757 kg·hm^-2;而玉/薯模式在180 kg·hm^-2、按底肥∶穗肥=5∶5的施肥方式下,氮素积累利用及产量均优于其他处理,两年平均产量为6572 kg·hm^-2,可实现两种模式下玉米高产、高效、安全的氮肥管理体系.
     

里氏木霉与米根霉混合固态发酵产纤维素酶

以里氏木霉及米根霉单菌固态发酵为对象,考察不同混合发酵形式对里氏木霉与米根霉混合固态发酵产纤维素酶的影响。结果表明:同时接种里氏木霉与米根霉,试验考察的两菌种接种量比1∶1(以孢子个数计)及5∶1条件下,两菌未产生明显协同产酶作用。米根霉延时(24 h)接种且菌种量比5∶1以及米根霉延时(48 h)接种且菌种量比1∶1,2种发酵形式产酶情况类似,滤纸酶活(FPA)及羧甲基纤维素酶(CMCase)酶活相对米根霉单菌发酵有所提高,而β-葡萄糖苷酶(β-GA)酶活相对里氏木霉单菌固态发酵结束时分别增加4.66及4.40倍,可以发现两菌产生一定协同作用。在米根霉延时(48 h)接种且菌种量比5∶1的发酵形式下,FPA及CMCase在发酵第7天酶活分别达到44.04 IU/g、627.14 U/g(以1 g干曲计),分别是里氏木霉固态单菌发酵产酶达到稳定期时酶活的1.36和1.63倍,两菌产生了有效的协同作用。     

树干毕赤酵母酒精发酵碳元素代谢流向分析

实验对树干毕赤酵母（Pichia stipitis）进行了4个阶段共400 h连续恒化培养,在不同阶段以30.0 g/L葡萄糖作为基本碳源,添加30.0或15.0 g/L的木糖,通过控制温度（35±1）℃,进气量100～150mL/min,搅拌转速250～300 r/min。4个阶段共建立4个连续培养的"稳态"。对碳元素进行物料衡算发现,四个阶段碳元素回收率分别为118.0 %、105.6 %、113.5 %和94.7 %。对4个近似"稳态"的碳元素的代谢流向进行分析发现：将近50.0 %左右碳元素流向产物酒精,其次是CO2和酵母细胞;木糖醇浓度与流入底物中木糖浓度有直接关系,在相同发酵条件下流入的木糖浓度越大代谢生成木糖醇浓度也越高;实验所采用的通气条件更适合底物为30.0 g/L葡萄糖和30.0 g/L木糖混合液的连续发酵。     

MORPHOLOGICAL STUDIES OF LYMNAEID SNAILS FROM THE HUMAN FASCIOLIASIS ENDEMIC ZONE OF BOLIVIA

The taxonomic position of the Lymnaeidae from the BolivianAltiplano has been unclear. On the basis of conchological characters,some authors reported two species from this area, Lymnaea viatrix andL. cubensis while others, considering also anatomical characters,considered L. viatrix as a synonym of L. cubensis. More recentstudies demonstrated genetic identity between the Bolivian lymnaeidsand L. truncatula from the Iberian Peninsula. Populations recognizedas L. cubensis correspond to a distinct genetic group, but geneticinformation was not available for L. viatrix. In the light ofthese genetic results, a morphometric study of both the shell (usingRaupian parameters) and male reproductive system was carried outof L. cubensis from Cuba (type locality), Dominican Republic,Guadeloupe and Venezuela, and of L. truncatula from Bolivia,France, Portugal, Spain and Morocco. Syntypes of L. viatrixfrom Argentina (var. A. ventricosa) and specimens of L. viatrix(var. B. elongata) from the type locality, Peru, were also studied(conchological characters only). The conchological study showedthe presence of a large amount of variability between populations.This variability was not congruent with genetic results. Alarge amount of variability was also found using anatomicalcharacters of the male reproductive system and all of them clearlyseparate L. cubensis from L. truncatula independently from geographicalorigin. Thus anatomical characters, unlike conchological parameters,do differentiate taxonomic species inferred from genetic studies. (Received 11 September 1997; accepted 5 March 1999)     

低聚木糖分离纯化的研究进展

综述了低聚木糖分离纯化的研究进展。低聚木糖是一种非消化性寡糖 ,能选择性增殖肠道内双歧杆菌 ,可广泛应用于食品工业和饲料工业。低聚木糖的分离纯化技术主要包括层析分离技术 (包括凝胶过滤层析、离子交换层析和吸附层析 )和膜分离技术 (包括超滤、纳滤和反渗透 )。低聚木糖的提纯主要采用膜分离技术和层析分离技术 ,低聚木糖单一组分的分离主要采用凝胶过滤层析和吸附层析     

白三叶TrFQR1基因克隆与表达分析

采用RACE和RT-PCR方法,克隆白三叶拉丁诺(Trifolium repens cv.‘Ladino’)的cDNA基因序列,命名为TrFQR1,对该序列进行生物信息学分析,利用实时荧光定量PCR检测TrFQR1的表达模式。结果表明:(1)TrFQR1序列长为1 003bp,开放阅读框为612bp,编码203个氨基酸,该蛋白的理论分子质量21.88kD,等电点为5.96,属于亲水性稳定蛋白,无信号肽,无跨膜结构域,在进化上高度保守,N端11~15位氨基酸和C端112~165位氨基酸是FMN结合位点。(2)TrFQR1表达模式分析显示,白三叶TrFQR1基因对于8种处理均有响应,但不同处理响应不同,其中:用25μmol/L SNP、10mmol/L H_2O_2、5mmol/L CaCl_2处理1.5h以及15%PEG处理3h时,白三叶TrFQR1基因相对表达量显著增加;在200mmol/L NaCl和600μmol/L CdSO4处理下,TrFQR1基因相对表达量随处理时间的增加而增加;4℃处理6h和0.02mmol/L NaHS处理1.5h时,TrFQR1基因相对表达量显著减少。     

饲料营养成分对草鱼,团头鲂和青鱼鱼种阶段的饲料可消化能值的影响

为了探讨饲料可消化能值同饲料营养成分之间的关系,用Ｃｒ２Ｏ３作指示物,分别测定了鱼粉和大豆粕等饲料原料的草鱼（Ｃｔｅｎｏｐｈａｒｙｎｇｏｄｏｎ　ｉｄｅｌｌａ）团头鲂（Ｍｅｇａｌｏｂｒａｍａ ａｍｂｌｙｏｃｅｐｈａｌａ　Ｙｉｈ）青鱼（Ｍｙｌｏｐａｒｙｎｇｏｄｏｎ　ｐｉｃｅｕｓ）鱼种饲料的可消化能,用微机计算分析测试结果,发现饲料可消化能值随饲料蛋白质和／或脂肪食量增加而增加;随饲料无氮浸出物和／或纤维含量增加而降低。同时,“优选”出了有一定实用价值的估算草鱼、团头鲂和青鱼鱼种饲料可消化能值的回归方程。     

Increment of hFIX expression with endogenous intron 1 in Vitro

This paper probes into the feasibility of increasing expression level of hFIX gene with endogenous intron 1 sequence.hFIX minigene was obtained with middle sequence truncated intron 1 inserted into the relative site of hFIX cDNA,and plasmid vector pKG5i‘IX,retroviral vector G1NaCi‘IX were constructed.These vectors were transduced into target cells of PA317,C2C12,primary rabbit skin fibroblasts (RSF) and primary human skin fibroblasts (HSF).The expression level of mixed colonies are PA317/pKG5i‘IX,151 ng/10^6 cells/24h;PA317/G1NaCi‘IX,308 ng/10^6 cells/24 h;C2C12/G1NaCi‘IX,186 ng/10^6 cells/24 h;RSF/G1NaCi‘IX,1929 ng/10^6 cells/24 h;HSF/G1NaCi‘IX,1646 ng/10^6 cells/24 h.These results indicated that hFIX minigene with intron l is able to increase the expression level to about 3 times of that of hFIX cDNA.Meanwhile,in order to study the application of hFIX minigene in the retroviral-mediated gene transfer system and refrain from intron splicing during viral production,a retroviral vector G1NaCi‘IXR with reversely inserted hFIX minigene expression cassette was constructed.The expression level of reverse constructor in PA317 cells was 390 ng/10^6 cells/24 h with 79% of bioactivity.PCR detection of HT/G1NaCi‘IXR cells infected with PA317/G1NaCi‘IXR supernatant confirmed the existence of intron 1 sequence.These results suggested that expression vector with forward-inserted intronl-carrying hFIX expression cassette can be used in directed gene transfer,but when using the retroviral-mediated gene transfer system,reversely-inserted intronl-carrying hFIX expression cassette should be considered.     

Human chromosome pellicle antibody recognizing centromere protein-C (CENP-C), the main component of the kinetochore

INTRODUCTIONDuringnormalcelldivision,thechromosomesplitsevenly,givingthesamegeneticmaterialtoeachdaughtercell.Theaccuracyofsuchcelldivisiondependsontheinteractionbetweenthespindleapparatusandtheets--actingregionofeachchromosomeknownasthecentromere.Manyessentialmitoticfunctionsoccuratorarecontrolledbythecentromere.Capturingspindlemicrotubules,thegrowthanddisassemblyofmicrotubules,theliningupofchromosomesonthemetaphaseplate,andthesplittingoffofthesisterchromatidsduringmitosisareallsomehowre…