麻疯树G蛋白γ亚基JcAGG3基因的克隆及表达分析

从麻疯树c DNA中克隆到一个与拟南芥AGG3同源的基因,命名为Jc AGG3。该基因开放阅读框为834bp,编码277个氨基酸,软件预测等电点为8.61,分子质量为30.514k Da。亚细胞定位预测显示其定位于细胞质膜上。在该基因的顺势作用元件上发现了与胚乳发育、激素调节、光响应和逆境胁迫相关的启动元件。荧光定量PCR(q PCR)检测发现,Jc AGG3在根、茎、叶和种子中均有表达,在发育中的种子中表达量最高,幼叶中的表达量显著高于老叶,在茎中只检测到极微量的表达;对麻疯树的幼苗进行黑暗处理后Jc AGG3基因表达显著下调,脱落酸(ABA)和干旱胁迫处理下Jc AGG3表达量显著增加。     

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.
     

控制性分根交替灌溉下氮形态对番茄生长、果实产量及品质的影响

以高产大果型西红柿品种中研988为材料,采用分根培养的方法,研究了控制性分根交替灌溉(APRI)条件下,不同氮素形态(硝态氮、铵态氮)对番茄生长、产量及果实品质的影响.结果表明: 同一灌溉方式或下限处理下,铵态氮对番茄植株前期生长有利,而硝态氮促进番茄植株后期生长,并促进果实产量增加.在APRI同一灌水下限下,硝态氮处理可提高果实维生素C含量及糖酸比,提高营养品质.同一氮素形态供应下,APRI番茄的株高和叶面积均小于正常灌溉(CK),但灌水下限为60%田间持水量(θ_f)的APRI处理番茄茎粗在生长后期有所增加.在同一氮素形态下,与CK相比,APRI各处理的产量均下降,其中灌水下限在40%θ_f的APRI处理产量下降了22.4%～26.3%;而灌水下限在60% θ_f的APRI处理仅下降了5.3%～5.4%,下降幅度相对较小,而品质显著提高,并具有明显的节水效果.因此,控制灌水下限在60%θ_f、供应硝态氮的APRI处理为番茄高产、优质、节水的最佳处理.
     

典型亚热带热分层水库秋季细菌群落垂直分布

水库在我国东南沿海地区是重要的饮用水水源地,对地区经济发展和社会稳定起到重要作用。选择亚热带地区典型的热分层水库——福建莆田东圳水库,于2011年秋季稳定分层期,以水体温度的垂直变化特征为依据进行分层采样。应用PCRDGGE和克隆测序的方法研究浮游细菌群落的垂直分布特征,利用多元统计分析揭示细菌群落与热分层水体理化指标之间的关系。结果显示:溶解氧、电导率、叶绿素a、总氮、氨氮及硝氮在上下层水体中的分布有显著差异,下层缺氧区细菌的ShannonWiener指数和DGGE条带数明显高于上层好氧区,表明东圳水库热分层水体中存在明显的物理、化学及生物分层现象。测序结果表明β-变形菌可能是东圳水库中占优势的细菌类群,统计结果提示溶解氧是显著影响细菌群落组成的环境因子。热分层水体的物理化学分层与水体细菌群落结构密切相关,提示水库生态学研究应对水体热分层给予重视。     

葡萄糖氧化酶基因片段的克隆与序列分析

根据Gen Bank发布的葡萄糖氧化酶基因序列设计PCR扩增引物,从筛选的1株可以产生葡萄糖氧化酶的菌株中克隆得到葡萄糖氧化酶基因片段,将该片段与p MD20-T载体连接后转化至大肠埃希菌DH5α中,测序并进行序列比对分析。结果表明,该克隆片段属于氧化还原酶超家族,且与同属氧化还原酶超家族中的Aspergillus niger strain BT18葡萄糖氧化酶相似度达到92%。从蛋白质预测的三级结构可以看出有FAD和NAG结合位点,说明该GOD片段理论上可以表达出GOD的主要功能。可以推断该克隆的基因片段为葡萄糖氧化酶基因片段。     

A 38 nt region and its flanking sequences within gag of Friend murine leukemia virus are crucial for splicing at the correct 5′ and 3′ splice sites

The genome of the Friend murine leukemia virus (Fr‐MLV) contains a 5′ splice site (5′ss) located at 205 nt and a 3′ss located at 5489 nt. In our previous studies, it was shown that if the HindIII–BglII (879–1904 bp) fragment within gag is deleted from the proA8m1 vector, which carries the entire Fr‐MLV sequence, then cryptic splicing of env‐mRNA occurs. Here, attempts were made to identify the genomic segment(s) in this region that is/are essential to correct splicing. First, vectors with a serially truncated HindIII–BglII fragment were constructed. The vector, in which a 38 bp fragment (1612–1649 bp) is deleted or reversed in proA8m1, only produced splice variants. It was found that a 38 nt region within gag contains important elements that positively regulate splicing at the correct splice sites. Further analyses of a series of vectors carrying the 38 bp fragment and its flanking sequences showed that a region (1183–1611 nt) upstream of the 38 nt fragment also contains sequences that positively or negatively influence splicing at the correct splice sites. The SphI–NdeI (5140–5400 bp) fragment just upstream of the 3′ss was deleted from vectors that carried the 38 bp fragment and its flanking sequences, which yielded correctly spliced mRNA; interestingly, these deleted vectors showed cryptic splicing. These findings suggest that the 5140–5400 nt region located just upstream of the 3′ss is required for the splicing function of the 38 nt fragment and its flanking sequences.     

Experimental selection of long‐term intracellular mycobacteria

Some intracellular bacteria are known to cause long‐term infections that last decades without compromising the viability of the host. Although of critical importance, the adaptations that intracellular bacteria undergo during this long process of residence in a host cell environment remain obscure. Here, we report a novel experimental approach to study the adaptations of mycobacteria imposed by a long‐term intracellular lifestyle. Selected Mycobacterium bovis BCG through continuous culture in macrophages underwent an adaptation process leading to impaired phenolic glycolipids (PGL) synthesis, improved usage of glucose as a carbon source and accumulation of neutral lipids. These changes correlated with increased survival of mycobacteria in macrophages and mice during re‐infection and also with the specific expression of stress‐ and survival‐related genes. Our findings identify bacterial traits implicated in the establishment of long‐term cellular infections and represent a tool for understanding the physiological states and the environment that bacteria face living in fluctuating intracellular environments.