Phytoremediation of Metals Using Transgenic Plants

An ideal plant for environmental cleanup can be envisioned as one with high biomass production, combined with superior capacity for pollutant tolerance, accumulation, and/or degradation, depending on the type of pollutant and the phytoremediation technology of choice. With the use of genetic engineering, it is feasible to manipulate a plant's capacity to tolerate, accumulate, and/or metabolize pollutants, and thus to create the ideal plant for environmental cleanup. In this review, we focus on the design and creation of transgenic plants for phytoremediation of metals. Plant properties important for metal phytoremediation are metal tolerance and accumulation, which are determined by metal uptake, root-shoot translocation, intracellular sequestration, chemical modification, and general stress resistance. If we know which molecular mechanisms are involved in these tolerance and accumulation processes, and which genes control these mechanisms, we can manipulate them to our advantage. This review aims to give a succinct overview of plant metal tolerance and accumulation mechanisms, and to identify possible strategies for genetic engineering of plants for metal phytoremediation. An overview is presented of what has been achieved so far regarding the manipulation of plant metal metabolism. In fact, both enhanced metal tolerance and accumulation have been achieved by overproducing metal chelating molecules (citrate, phytochelatins, metallothioneins, phytosiderophores, ferritin) or by the overexpression of metal transporter proteins. Mercury volatilization and tolerance was achieved by introduction of a bacterial pathway. The typical increase in metal accumulation as the result of these genetic engineering approaches is 2-to 3-fold more metal per plant, which could potentially enhance phytoremediation efficiency by the same factor. As for the applicability of these transgenics for environmental cleanup, results from lab and greenhouse studies look promising for several of these transgenics, but field studies will be the ultimate test to establish their phytoremediation potential, their competitiveness, and risks associated with their use.     

Addition of nickel to Murashige and Skoog medium in plant tissue culture activates urease and may reduce metabolic stress

Nickel has been identified as an essential element for plant growth. The lack of nickel and the inclusion of cobalt leads to absence of urease activity in plants grown on MS medium in tissue culture. To avoid leaf damage and metabolic stress, nickel should be included in tissue culture growth media.     

Cesium Doped NiOx as an Efficient Hole Extraction Layer for Inverted Planar Perovskite Solar Cells

Organic–inorganic hybrid perovskite solar cells have resulted in tremendous interest in developing next generation photovoltaics due to high record efficiency exceeding 22%. For inverted structure perovskite solar cells, the hole extraction layers play a significant role in achieving efficient and stable perovskite solar cell by modifying charge extraction, interfacial recombination losses, and band alignment. Here, cesium doped NiO_x is selected as a hole extraction layer to study the impact of Cs dopant on the optoelectronic properties of NiO_x and the photovoltaic performance. Cs doped NiO_x films are prepared by a simple solution‐based method. Both doped and undoped NiO_x films are smooth and highly transparent, while the Cs doped NiO_x exhibits better electron conductivity and higher work function. Therefore, Cs doping results in a significant improvement in the performance of NiO_x‐based inverted planar perovskite solar cells. The best efficiency of Cs doped NiO_x devices is 19.35%, and those devices show high stability as well. The improved efficiency in devices with Cs:NiO_x is attributed to a significant improvement in the hole extraction and better band alignment compared to undoped NiO_x. This work reveals that Cs doped NiO_x is very promising hole extraction material for high and stable inverted perovskite solar cells.     

Active Edge Sites Engineering in Nickel Cobalt Selenide Solid Solutions for Highly Efficient Hydrogen Evolution

An effective multifaceted strategy is demonstrated to increase active edge site concentration in Ni_0.33Co_0.67Se₂ solid solutions prepared by in situ selenization process of nickel cobalt precursor. The simultaneous control of surface, phase, and morphology result in as‐prepared ternary solid solution with extremely high electrochemically active surface area (C _dl = 197 mF cm^?2), suggesting significant exposure of active sites in this ternary compound. Coupled with metallic‐like electrical conductivity and lower free energy for atomic hydrogen adsorption in Ni_0.33Co_0.67Se₂, identified by temperature‐dependent conductivities and density functional theory calculations, the authors have achieved unprecedented fast hydrogen evolution kinetics, approaching that of Pt. Specifically, the Ni_0.33Co_0.67Se₂ solid solutions show a low overpotential of 65 mV at ?10 mV cm^?2, with onset potential of mere 18 mV, an impressive small Tafel slope of 35 mV dec^?1, and a large exchange current density of 184 µA cm^?2 in acidic electrolyte. Further, it is shown that the as‐prepared Ni_0.33Co_0.67Se₂ solid solution not only works very well in acidic electrolyte but also delivers exceptional hydrogen evolution reaction (HER) performance in alkaline media. The outstanding HER performance makes this solid solution a promising candidate for mass hydrogen production.     

镍胁迫下安氏伪镖水蚤SSH文库的构建及铁蛋白cDNA的克隆与差异表达

为探讨镍胁迫下桡足类的分子响应机制,以安氏伪镖水蚤为研究对象,利用抑制性消减杂交(suppression subtractive hybridization,SSH)技术,构建了镍胁迫下安氏伪镖水蚤SSHcDNA文库,并随机挑取生长菌落140个克隆子,进行菌液PCR鉴定,计算文库重组率为98.6％,文库容量为1.12×106 cfu.将重组子测序,经BLAST一致性搜索比对分析发现,有一重组片段含有铁蛋白保守结构域,该片段大小为859 bp,连续编码170个氨基酸残基,Gen-Bank登录号为JK312601.半定量PCR证实,镍胁迫24 h后,安氏伪镖水蚤中铁蛋白表达显著上调.本文库的成功构建及铁蛋白cDNA片段的获得为进一步研究镍胁迫下桡足类的分子响应机制奠定了基础.     

Acacia nilotica L. Bark Removes Toxic Elements from Solution: Corroboration from Toxicity Bioassay Using Salix viminalis L. in Hydroponic System

The present investigation deals with the advantages and potential of the Acacia nilotica bark as an adsorbent of toxic metals. Bark (1 g) when added to 100 ml of aqueous solution containing 10 μg ml^-1 metal solution exhibited different metal adsorption values for different metals. The order of metal adsorption being Cr ≥ Ni > Cu > Cd > As > Pb. A similar trend of metal adsorption was observed when the bark is reused (1^st recycle) Cr> Ni > Cu > Cd > Pb and also in the column sorption. In order to verify the metal removal property of A. nilotica bark, toxicity bioassay with Salix viminalis stem cuttings in hydroponic system augmented with Cd, Cr, and Pb together with A. nilotica bark powder was carried out. The results of toxicity bioassay confirmed the metal adsorption property of the bark powder. The functions of toxicity studies include leaf area, root length and number of new root primordia produced per stump. The leaf area, root length, and the number of new root primordia increased considerably in the presence of A. nilotica bark. The order of metal toxicity for leaf area and new root primordial is Cd > Cr > Pb. However, for root length the order of metal toxicity is Cr > Cd > Pb. The metal budgets of the leaf and root confirmed that the bark powder had adsorbed substantial amount of toxic metals and thus alleviates the toxicity imposed by the various tested elements. Hence, the utility of A. nilotica bark in developing and designing innovative technology for the clean up of toxic elements in aqueous solutions and possible scope for its use in phytoremediation are discussed.     

Metal uptake by iron-efficient and inefficient oats

Metal uptake by oats depending on plant responses to Fe-deficiency stress was investigated. Coker 227 oats classified as Fe-efficient and TAM 0–312 oats as Fe-inefficient cultivars (Hopkins et al., 1992) were grown either alone or in combination in three sandy soils using a pot experiment. These soils were from a field trial with sludge-borne metals applications leading to an increased metal content. Plant shoots were harvested one month after growth. Because soil pH increased from 5.4 to 6.8, shoot Fe level decreased in the Fe-inefficient TAM 0–312 oats compared to Coker 227 oats when plants were grown alone. In combination, TAM 0–312 oats had a negative impact on the availability of Fe in the Fe-efficient Coker 227 oats. Especially, Coker 227 and TAM 0–312 shoots showed chlorosis in mixed culture with high Zn and Mn content in the soil (soil B). However, Fe content in TAM 0–312 shoots in mixed culture did not increase compared to monoculture in all soils. In metal-contaminated soils, TAM 0–312 oats grown alone obtained less Zn and Cd than Coker 227 oats. Additionally at soil pH 6.8, shoot Ni and Mn levels were also lower in TAM 0–312 oats than in Coker 227 oats. Shoot Zn, Cd, and Ni levels decreased in Coker 227 oats from mixed cultures, and were not different compared to those in TAM 0–312 oats. Cu uptake was similar in all treatments except for the mixed culture in soil B. Coker 227 oats have been found to release a phytosiderophore whereas TAM 0–312 did not (Brown et al., 1991). Results indicated that phytosiderophores may lead to a higher Zn, Cd and Ni supply in the rhizosphere of Coker 227 oats and to higher metal contents in their shoots than in TAM 0–312 oats which did not activate such mechanisms.     

Experimental Assessment of Using Soluble Humic Substances for Remediation of Heavy Metal Polluted Soils

Since heavy metals are nondegradable and strongly bonded in soils, remediation of heavy metal polluted soils by extraction is difficult and current extraction techniques require harsh chemicals such as ethylenediaminetetraacetic acid (EDTA). However, use of EDTA is environmentally problematic because of costs, persistence, toxicity and deterioration of soil structure. Therefore, the potential of soluble natural humic substances (HS) to extract heavy metals from contaminated soils is tested as an environmentally friendly substitute for EDTA. A strongly polluted, calcareous urban soil (CRC soil) and a moderately polluted agricultural soil (CUP soil) were extracted at neutral pH in batch mode by three HS solutions from beech and Norway spruce litter (Beech-HS and Spruce-HS) and processed cow slurry (Bio-HS), all containing 25 mM dissolved organic carbon (DOC). After 10 extractions with a solution to soil ratio of 5:1 (L/kg), 8% to 39% of the total Cd, Cu, Ni and Pb soil contents, lowest for Ni and highest for Cu/Pb, were extracted. Natural and processed HS samples had comparable capacities to extract the heavy metals. A comparison of 100 mM DOC of Bio-HS and EDTA as extractants for Cu from the CRC soil showed extraction of 67% by EDTA and 41% by Bio-HS, indicating somewhat higher efficiency of EDTA than of HS. Sequential extraction of the CRC soil after Bio-HS and EDTA extraction showed removal of exchangeable, carbonate- and metal oxide-bound Cu but also of some residual Cu. It is therefore concluded that HS appears to be an attractive and promising alternative to EDTA as remediation agent for heavy metal polluted soils provided cheap HS of good quality is easily available.     

Ni2+对不同发育阶段斜纹夜蛾虫体血淋巴能量物质的影响

研究了饲料中不同浓度的Ni2+(140mg/kg)对连续3个世代斜纹夜蛾Spodoptera litura Fabricius6龄末幼虫、蛹和成虫血淋巴中能量物质总糖、蛋白质和脂肪含量及血淋巴中热量值的影响。结果表明,Ni2+胁迫1个世代,6龄末幼虫、蛹和成虫血淋巴中的总糖含量均低于对照,而血淋巴中的蛋白质含量则在低浓度Ni2+胁迫下增高,在高浓度Ni2+胁迫下降低;只有受120mg/kg Ni2+胁迫的6龄末幼虫血淋巴的脂肪含量高于对照,而蛹和成虫血淋巴中的脂肪含量及热量值均低于对照。在Ni2+胁迫的第2、3代,6龄末幼虫、蛹和成虫血淋巴中的总糖、蛋白含量和热量值与饲料中Ni2+浓度的反应关系均表现为低浓度Ni2+胁迫增加而高浓度Ni2+胁迫降低的趋势;然而,血淋巴中的脂肪含量随饲料中Ni2+浓度的增加而降低。因此,重金属Ni2+对S.litura能量物质的影响与虫体内能量物质的种类和虫体的发育阶段有一定的关联。