用纸浆代棉花合成CMC

羧甲基纤维素(CMC)系天然纤维素的衍生物。它是由天然纤维素分子上引入强极性羧甲基钠而得到的。我们采用纸浆为原料替代棉花生产CMC,测试了其性能,并讨论了反应温度、反应时间和碱用量对粘度的影响。结果表明:此法简化了工艺,原料来源广泛,产品性能优良,成本低,能满足使用要求。     

荒漠草原生态恢复与重建：人工植被推动下水分介导的系统响应、生态阈值与互馈作用

荒漠草原(生态区)横贯我国西北地区东部,生态地位十分重要。近二十年来,通过封育禁牧、退耕还林(草),植被覆盖显著改善,但是生态系统质量和稳定性依然不高。由于长期将荒漠草原单纯视作草原的一部分,对其生态系统过渡性、脆弱性和复杂性本质特征认识不足,造成了荒漠草原生态学研究与区域生态建设实践之间不同程度的脱节。在分析荒漠草原生态区未来在我国生态安全格局中突出的但是被一定程度上忽视的地位的基础上,进一步归纳了荒漠草原生态系统的一般特征,指出了生态恢复与重建研究中存在的主要问题。进而以人工植被引入荒漠草原生态工程为案例,分析了人工植被驱动荒漠草原生态恢复与重建的过程与机制,归纳了“植被-水文-土壤”互馈作用驱动生态系统层级响应模式,并展望了今后的发展趋势与研究方向。     

真菌传杆状病毒组（Furovirus）内四种病毒的细胞病理学比较研究

本文研究丁真菌传杆状病毒组（Ｆｕｒｏｖｉｒｕｓ）四个病毒成员,即甜菜坏死黄脉病毒（ＢＮＹＶＶ）、甜菜土传病毒（ＢＳＢＶ）、花生丛生病毒印度株系（ＰＣＡ－Ｉ）以及非洲株系（ＰＣＡ－Ａ）和小麦土传花叶病毒（ＳＢＷＭＶ）所引起的细胞病理变化。这四种病毒在病毒粒子聚集的结构,是否引起细胞膜聚集及聚集的结构,过氧化物酶体泡状物的形成与否及结构均有差异。另外,同一种病毒的不同株系或分离物所引起的细胞病理变化也不相同。     

不同条件下两株溶磷菌溶磷量及葡萄糖脱氢酶基因表达与酶活分析北大核心CSCD

【目的】获得大豆根际土壤中溶磷能力较强的菌株,明确在菌株溶磷过程中葡萄糖脱氢酶(GDH)的作用特点及其基因的表达水平。【方法】利用溶磷圈方法分离与纯化溶磷菌株,采用Vitek 2系统和16S r RNA序列分析菌株的分类地位;测定2菌株的溶磷量、GDH活性,并根据GDH基因的保守区序列设计引物,克隆GDH基因,利用实时荧光定量PCR测定不同条件下基因的相对表达量。【结果】筛选出2株具有较强溶磷能力的溶磷菌,分别鉴定为Pseudomonas sp.和Enterobacter sp.,2菌株最高溶磷量分别为558μg/m L和478μg/m L;成功地克隆了2株溶磷菌的GDH基因,片段大小分别为2007 bp和2066 bp;2菌株在不同磷源、不同p H值培养基中GDH活性及基因表达量不同,菌株wj1在高磷条件下基因表达量最高,磷胁迫条件下基因表达量较低,而wj3在不同磷源条件下GDH基因表达量都较低。且GDH基因表达量及酶活的变化与wj3菌株溶磷量没有直接的关系。【结论】从大豆根际土壤中分离获得溶磷能力较强的菌株Pseudomonas sp.wj1和Enterobacter sp.Wj3,GDH活性及基因表达在2株菌溶磷过程中具有不同的作用特点,2菌株溶磷机制不完全相同。     

Evidence for an Important Role of WRKY DNA Binding Proteins in the Regulation of NPR1 Gene Expression

The Arabidopsis NPR1 gene is a positive regulator of inducible plant disease resistance. Expression of NPR1 is induced by pathogen infection or treatment with defense-inducing compounds such as salicylic acid (SA). Transgenic plants overexpressing NPR1 exhibit enhanced resistance to a broad spectrum of microbial pathogens, whereas plants underexpressing the gene are more susceptible to pathogen infection. These results suggest that regulation of NPR1 gene expression is important for the activation of plant defense responses. In the present study, we report the identification of W-box sequences in the promoter region of the NPR1 gene that are recognized specifically by SA-induced WRKY DNA binding proteins from Arabidopsis. Mutations in these W-box sequences abolished their recognition by WRKY DNA binding proteins, rendered the promoter unable to activate a downstream reporter gene, and compromised the ability of NPR1 to complement npr1 mutants for SA-induced defense gene expression and disease resistance. These results provide strong evidence that certain WRKY genes act upstream of NPR1 and positively regulate its expression during the activation of plant defense responses. Consistent with this model, we found that SA-induced expression of a number of WRKY genes was independent of NPR1.     

Trans‐3,5,4´‐trimethoxystilbene reduced gefitinib resistance in NSCLCs via suppressing MAPK/Akt/Bcl‐2 pathway by upregulation of miR‐345 and miR‐498

Despite initial dramatic efficacy of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (EGFR‐TKIs) in EGFR‐mutant lung cancer patients, subsequent emergence of acquired resistance is almost inevitable. Resveratrol and its derivatives have been found to exert some effects on EGFR‐TKI resistance in non‐small cell lung cancer (NSCLC), but the underlying mechanisms remain unclear. We screened several NSCLC cell lines with gefitinib resistance by MTT assay and analysed the miR‐345/miR‐498 expression levels. NSCLC cells were pre‐treated with a resveratrol derivative, trans‐3,5,4‐trimethoxystilbene (TMS) and subsequently challenged with gefitinib treatment. The changes in apoptosis and miR‐345/miR‐498 expression were analysed by flow cytometry and q‐PCR respectively. The functions of miR‐345/miR‐498 were verified by CCK‐8 assay, cell cycle analysis, dual‐luciferase reporter gene assay and immunoblotting analysis. Our results showed that the expression of miR‐345 and miR‐498 significantly decreased in gefitinib resistant NSCLC cells. TMS pre‐treatment significantly upregulated the expression of miR‐345 and miR‐498 increasing the sensitivity of NSCLC cells to gefitinib and inducing apoptosis. MiR‐345 and miR‐498 were verified to inhibit proliferation by cell cycle arrest and regulate the MAPK/c‐Fos and AKT/Bcl‐2 signalling pathways by directly targeting MAPK1 and PIK3R1 respectively. The combination of TMS and gefitinib promoted apoptosis also by miR‐345 and miR‐498 targeting the MAPK/c‐Fos and AKT/Bcl‐2 signalling pathways. Our study demonstrated that TMS reduced gefitinib resistance in NSCLCs via suppression of the MAPK/Akt/Bcl‐2 pathway by upregulation of miR‐345/498. These findings would lay the theoretical basis for the future study of TMS for the treatment of EGFR‐TKI resistance in NSCLCs.     

甲状腺激素对胸腺上皮细胞CK19蛋白表达的影响

目的探讨甲状腺激素对胸腺的发育的影响及可能的机制。方法将12只怀孕4d的大鼠随机分成A组和B组,A组正常饮水,B组孕鼠供以含有0．02％甲巯咪唑的饮水制备仔鼠甲状腺功能低下动物模型,将A组的仔鼠随机分成对照组和甲状腺素钠组,将B组的仔鼠随机分成甲低组和甲低＋甲状腺素钠组。甲状腺素钠组和甲低＋甲状腺素钠组于出生后15d给予腹腔注射甲状腺素钠（0．5mg／kg体重,1次／d）,连续给药25d。所有动物于出生后40d麻醉处死,测定仔鼠的胸腺重量及脏器指数;采用放射免疫技术测定仔鼠血清中三碘甲状腺原氨酸（triiodothyronine,T3）、四碘甲状腺原氨酸（tetraiodothyronine,T4）、促甲状腺激素（thyroid—stimulating hormone,TSH）水平,免疫组织化学技术检测胸腺上皮细胞细胞角蛋白19（cytokeratin 19,CK19）蛋白的表达量。结果与对照组比较,甲状腺素钠组仔鼠血清中T3、T4显著升高,TSH减少,胸腺重量增大;甲低组仔鼠血清中T3、T4明显降低,TSH显著增高,胸腺重量降低,胸腺上皮细胞CK19蛋白表达减少。与甲低组比较,甲低＋甲状腺素钠组仔鼠血清中T3、T4升高,TSH降低,胸腺指数增大,胸腺上皮细胞CK19蛋白的表达明显增多。结论甲状腺激素可以通过影响胸腺上皮细胞CK19的表达量,使胸腺发育或退化。     

水溶性有机物在水旱轮作土壤剖面中的分馏现象

水溶性有机物(DOM)是有机物质中最为活跃的组成部分,在陆地生态系统物质的迁移转化过程中起重要作用．通过田间试验和室内理化分析证明了DOM在土壤剖面迁移过程中存在明显的“分馏”现象,随着土层深度的增加,对照、施化肥和施污泥处理土壤DOM的浓度分别由145．8、117．7和114．8mg·kg^-1降到21．57、23．23和13．78mg·kg^-l;不施肥和施化肥处理的土壤DOM随着深度的增加,极性物质所占的比例分别由19．01％和18．47％增至34．97％与44．37％,呈上升趋势,而非极性组分所占比例相应降低;施污泥处理则出现相反的规律,极性组分由36．96％降到17．07％,非极性组分由63．04％增为82．93％．土壤DOM的生物降解率由上到下对照和施化肥处理分别由24．38％和24．00％增大到54．74％和53．81％,而施污泥处理的变化规律则相反,由53．19％降到30．75％．DOM的生物降解率与DOM中极性物质的含量呈正相关关系．紫外光谱进一步证实了这一结果．     

地下水位对黄河三角洲柽柳根系生长的影响

为揭示黄河三角洲柽柳根系生长特征对地下水位的响应规律,明确柽柳生长适宜的地下水位,在咸水矿化度（6 g/L）下,模拟设置0、0.3、0.6、0.9、1.2、1.5、1.8 m共7个地下水位。测定分析栽植柽柳土柱的水盐参数与根系生长指标。结果表明：在咸水矿化度下,地下水位可显著影响土壤水盐变化,从而影响柽柳根系的生长。随地下水位的降低,土壤含水量、含盐量和土壤溶液绝对浓度显著降低。在高水位（≤0.6 m）下,柽柳根系生长受水盐胁迫影响显著,柽柳根长、根径、侧根数、总生物量、侧根生物量、根系连接长度均较低,拓扑结构呈叉状分支;中水位（0.9 m）时,土壤水盐条件适宜,柽柳侧根数、根径、二级侧根和毛细根生物量达到最大值,拓扑结构由叉状分支向鱼尾形分支过渡;低水位（≥1.2 m）下,土壤水盐含量低,柽柳根系总生物量、主根生物量、一级侧根生物量和根系平均连接长度在1.2 m水位达到最大值后降低,拓扑结构呈鱼尾形分支。柽柳根系生长与地下水位密切相关,柽柳通过改变根系生长和调整构型来适应不同土壤水盐和地下水位条件。高水位（≤0.6 m）下柽柳以降低根系生长深度,增加分叉,调配各组织器官的生物量来适应水盐胁迫;中水位0.9 m下土壤水盐条件最适宜柽柳生长;低水位（≥1.2 m）下柽柳主要受土壤干旱胁迫而使根系向下生长,增加根系连接长度,以此扩大资源获取效率。柽柳根系生长及根系构型对咸水矿化度下不同地下水位表现出较强的适应性和可塑性。