5 resultados para Ricinus communis L.

em Chinese Academy of Sciences Institutional Repositories Grid Portal


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植物-微生物联合修复是利用微生物作为植物修复重金属土壤的一种强化手段,在弥补单纯植物及微生物修复技术不足的同时,利用植物和微生物的共存体系提高植物修复效率。本研究考察了向日葵(Helianthus annuus L.),芥菜(Brassica juncea L.),紫花苜蓿(Medicago sativa L.)和蓖麻(Ricinus communis L.)对Cd、Pb的富集特征,并筛选出向日葵作为富集植物;探讨了向日葵根系分泌物在重金属胁迫下的变化;通过重金属耐受菌株与向日葵的配伍对Cd、Pb污染土壤进行联合修复,结果如下: 液体培养实验结果表明,四种植物对Cd、Pb富集能力明显不同,其中向日葵对两种重金属的提取效果较好。四种植物对重金属的富集量随着浓度的增加而增加,而富集系数随重金属浓度的增加而减小,转移系数同重金属浓度及地上部/地下部生物量比值呈现一定的相关性;Cd、Pb复合处理中,一种重金属的存在会在不同程度上影响植物对另一种重金属的吸收;此外,不同植物及重金属处理中根际区域的酸碱度及氧化还原电位呈现负相关性。 砂培实验结果表明,向日葵对重金属的富集规律基本同液体培养实验相似。富集系数与重金属浓度和培养时间呈现线性相关关系。复合处理中,当Cd和Pb在适当浓度比例时,向日葵可以增加对某一重金属的吸收效率。向日葵的根系分泌物组成因重金属的存在而明显减少,根系分泌物中的草酸、酒石酸、苹果酸、柠檬酸、乙酸及丁二酸含量随着不同浓度Cd、Pb而发生不规则变化。 在以根系分泌物作为唯一营养来源筛选重金属耐受菌株实验中,细菌和真菌对Cd及Pb的耐性及吸附效率不同。总体上看,微生物生物量随重金属浓度升高而降低,而重金属吸附量随浓度升高而增加,重金属复合毒性也减少了微生物对单一重金属的吸收;另外,培养基中酸碱度因微生物种类及重金属浓度而有所差异。 将筛选出的优势微生物与向日葵配伍处理Cd、Pb污染土壤的实验中,由于Cd、Pb污染模式及菌株种类的不同,微生物对向日葵吸收重金属的强化效果呈现很大差异,其中真菌对植物吸收重金属的强化能力较细菌强;同时,根系分泌物中6种有机酸的含量在不同处理中变化较大;在处理单一Cd或Pb污染的时候选用菌株B1、F1或混合菌B1+B2、F1+F2、B2+F1、B1+F2与向日葵配伍修复的效果较好;混合菌F1+F2、B1+F2、B2+F1的添加能较好的强化Cd、Pb复合污染中向日葵吸收重金属的能力。

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A novel biodegradable aliphatic poly(L-lactide-co-carbonate) bearing pendant acetylene groups was successfully prepared by ring-opening copolymerization of L-lactide (LA) with 5-methyl-5-propargyloxycarbonyl-1,3-dioxan-2-one (PC) in the presence of benzyl alcohol as initiator with ZnEt2 as catalyst in bulk at 100 degrees C and subsequently used for grafting 2-azidoethyl beta-D-glucopyranoside and 2-azidoethyl beta-lactoside by the typical "click reaction," that is Cu(I)-catalyzed cycloaddition of azide and alkyne. The density of acetylene groups in the copolymer can be tailored by the molar ratio of PC to LA during the copolymerization. The aliphatic copolymers grafted with sugars showed low cytotoxicity to L929 cells, improved hydrophilic properties and specific recognition and binding ability with lectins, that is Concanavalin A (Con A) and Ricinus communis agglutinin (RCA). Therefore, this kind of sugar-grafted copolymer could be a good candidate in variety of biomedical applications.

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In this study. lectin-conjugated gold nanoparticles (GNPs) were prepared by standard biotin-streptavidin chemistry. The lectin-conjugated GNPs call be used as ail indicator for studying the interaction of lectin with glycosyl complex on living cellular Surfaces due to the high affinity of the lectin with saccharides. The interactions of two well-known lectins (Ricinus communis agglutinin and concanavalin A) and three different cell lines (HeLa, 293, and 293T) were selected here to establish this assay. Highly binding affinity of R. communis agglutinin with cells was demonstrated by conventional microscopic and UV-visible spectroscopic Studies. In addition, the binding process can be inhibited by galactose, giving further proof of the binding mechanism. (c) 2009 Elsevier Inc. All rights reserved.

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本文以芦苇野生亲本和耐盐变异体为材料,比较了两者在形态、生理生化以及分子生物学特性上的差异,对耐盐变异体抗盐能力提高的机理作了初步的探讨。为了适应推广芦苇耐盐变异体的需要,进行了耐盐变异体快速繁殖的研究,建立了两种诱导丛生芽的技术系统。对耐盐变异体芦苇在滩涂上的利用作了有益的尝试。结果总结如下: 1.通过对芦苇野生亲本和耐盐变异体的基因组DNA用随机引物扩增分析,发现两者的基因组DNA在序列上存在着一定的差异,并克隆测序了几个对变异体而言是特异的标记序列。 2.生化分析发现,在盐胁迫下,两者在可溶性蛋白上存在着差异,芦苇耐盐变异体在胁迫下分别在20~30 kD和43~66.2 kD之间各有一条特异的蛋白带表达。而且变异体盐胁迫下在同工酶的表达上也与野生亲本有着显著的区别。 3.生理测定发现,芦苇耐盐变异体在200 mmol/L NaCl胁迫下光合作用要比野生亲本强,叶绿素测定的结果与此相吻合,在此浓度的胁迫下,变异体叶绿素含量受影响较小,而野生亲本的叶绿素含量明显降低。对两者胁迫前后的离子含量测定发现,虽然K+含量最多,但是植株内离子含量变化最大且增加最多的离子是Na+,而且变异体内Na~+增加的量比野生亲本高得多。另一个变化较大的是游离脯氨酸的含量,其变化情况类似于Na~+,在胁迫后脯氨酸含量增加明显,而且变异体内的增加量比野生亲本高。对变异体进一步的胁迫反应证实了Na+和脯氨酸含量变化与胁迫反应的密切联系。推测它们的这些变化与变异体抗盐能力提高密切相关。 4.将芦苇耐盐变异体的种子苗切去种壳和种子根,以此作为外植体,通过筛选大量的激素组合,最终建立了两种快繁技术系统(MP-A和MP-B)进行丛生芽诱导。两个系统都包含预处理和诱导两个主要步骤,其中预处理培养基激素组合是相同的(NAA 2~5 mg/L + 2,4-D 0.05 ~ 0.1 mg + BA 1mg/L,而诱导处理的培养基激素组合不同,分别为:MP-A的诱导处理的激素组合是将预处理的激素组合中的2,4-D去除即可;MP-B诱导处理的激素组合为1mg/L NAA + 0.05 ~0.1mg/L 2,4-D + 2~5mg/L BA. 两个系统都获得显著的丛生芽诱导效果。 5.在滩涂水产养殖中引入芦苇种植、发现耐盐芦苇能有效地降低水体污染和病害,实验了两种模式的种养殖方式:围隔模式和混合模式,初步结果表明混合模式效果较好。这一初中初步验证了芦苇对海水养殖的价值,对开发滩涂具有很大的意义,具有创新性。

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The adsorption Of DL-homocysteine (Hcy) and L-homocysteine thiolactone (HTL) on Au(1 1 1) electrode was investigated in 0.1 M HClO4 by cyclic voltammetry and in situ scanning tunneling microscopy (STM). Hcy and HTL molecules formed highly ordered adlayers on Au(1 1 1) surface. High-resolution STM images revealed the orientation and packing arrangement in the ordered adlayers. Hcy molecules formed (2root3 x 3root3)R30degrees adlayer structure and H-bonds between carboxyl groups were assumed to be responsible for the origin of tail-to-tail or head-to-head molecular arrangement, while HTL molecules formed (4 x 6) adlayer structure, and two different orientations and appearances in the ordered adlayer were found. Structural models were proposed for the two adlayers.