大气CO2浓度升高对不同层次水稻土有机碳稳定性的影响

研究大气CO₂浓度升高对不同层次土壤有机碳(SOC)稳定性的影响对深入理解高浓度CO₂下SOC转化具有重要意义.以FACE(Free Air Carbon-dioxide Enrichment)平台长期定位试验水稻土为研究对象,通过SOC物理分级及矿化培养试验,研究大气CO₂浓度升高对稻田SOC含量、颗粒有机质(POM)含量、SOC矿化强度和酶活性变化的影响,探讨CO₂浓度升高对不同层次稻田SOC稳定性的影响.结果表明:大气CO₂浓度升高对表层SOC含量无显著影响,但使表层土壤POM-C显著增加了93.7%,同时使表层土壤蔗糖酶和多酚氧化酶活性分别提高了61.1%和83.7%,从而降低了表层SOC稳定性;大气CO₂浓度升高对深层SOC含量及其稳定性均无显著影响.研究结果将有助于评估土壤固定和储备碳的能力,为今后温室效应下农田管理提供科学依据.     

新疆棉田土壤质量综合评价方法

以新疆主要棉区为研究对象,测定了哈密、博乐、昌吉、奎屯、石河子、阿克苏及喀什棉田土壤耕层的pH、盐分、有机质、全氮、速效磷、速效钾及Cr、Cu、Zn、As、Pb 共计11个指标,综合分析土壤理化性质和重金属含量,采用土壤质量综合指数(SQI)对新疆主要棉区棉田土壤质量进行综合评价.结果表明: 新疆棉区棉田土壤呈碱性,pH均值为7.87,盐分含量均值为3.44 g·kg^-1,为轻度盐化土壤,有机质和全氮含量均偏低,速效磷、速效钾含量较为丰富,与第二次全国土壤普查数据相比,土壤pH、盐分含量、有机质和全氮均呈下降趋势,土壤速效磷明显增长,部分地区土壤速效钾呈现出不同程度的升高趋势;Cr、Cu、Zn、As、Pb 5种重金属含量分别为45.88、40.66、68.30、12.88、16.68 mg·kg^-1,均未超过国家二级标准,但与新疆土壤元素背景值相比,Cu、Zn、As均有累积现象.当重金属内梅罗综合污染指数(PN)小于0.5时,土壤理化性质越好,土壤综合质量越好.土壤有机质、全氮、Cu、Zn和As是影响新疆棉区棉田土壤质量的重要因素.新疆棉区棉田土壤质量总体属于中等水平,昌吉、奎屯质量最高,SQI为0.52,阿克苏质量最低,SQI为0.31,不同棉区土壤质量呈现为:北疆>东疆>南疆.     

新鲜土壤样品储存温度和时间对不同形态氮素的影响

土壤氮素形态及含量具有重要的生态学研究意义,而土壤样品的储存对土壤氮素含量的准确测定有很大影响.为了选择合理的土壤样品储存方法,本研究以福建省建瓯市万木林保护区罗浮栲林土壤为研究对象,测定在不同温度(25、4和-20 ℃)、不同储存时间(0、7和30 d)下土壤铵态氮、硝态氮、总氮、可溶性有机氮、氨基酸氮含量和微生物生物量氮,以及冷冻后常温培养过程中的氮素含量.结果表明: 在7 d的储存时间内,除氨基酸氮以外,常温培养样品下其余的氮素含量均有所增加;与新鲜样品相比,冷藏、冷冻样品的所有氮素含量之间均无显著性差异,且氮素含量变化较常温培养下更加稳定.因低温储存样品有刺激氮矿化的效果,在30 d储存时间内,与新鲜样品相比,除可溶性有机氮外,冷藏、冷冻样品的所有氮素含量均显著升高;两种冷储存方法之间无显著差异.因此,新鲜样品带回实验室后应及时处理;如需要冷储藏,时间不要超过半个月.如果需要较长的储存时间,则需将样品放置于更低的温度(-40或-80 ℃).在对储存土壤样品进行培养试验之前,需要进行预培养处理.在预培养过程中,除硝态氮含量呈现先下降再迅速升高的趋势外,其余氮素均随着培养时间逐渐趋近于新鲜土壤样品含量,在培养一周左右恢复到与新鲜土壤样品氮含量最为接近的状态.结合已有研究,对野外取样和风干样品需要5～14 d的预培养,冷储存样品预培养时间不应少于一周.     

快速展示糖苷水解酶活性架构单点突变导致结合力变化的电泳技术

酶分子在长期进化过程中形成一系列氨基酸残基组成的活性架构,参与底物的识别、结合与催化过程,而活性架构中相应氨基酸残基是如何影响酶分子结合底物的能力,进而影响酶分子的催化效率,一直是酶分子理性改造研究的热点.利用亲和电泳技术,可以快速展示内切纤维素酶Tr Cel12A和木聚糖酶Tl Xyn A活性架构中不同突变体的催化活性及其迁移率的变化,进而通过在不同底物浓度凝胶中蛋白质相对迁移率变化程度的定量回归分析,发现由氨基酸单点突变导致蛋白质迁移率的相对变化,可以定量表征酶分子突变前后结合底物能力的变化.亲和电泳测定的有效阻滞常数Kb值与等温滴定量热法和荧光光谱法测定的相关参数比较具有明显相关性.由于亲和电泳技术在测定酶分子与底物的结合能力时具有简便、快速、灵敏的特点,因而可作为常规生化实验室常规普筛技术来检测突变文库中系列突变体导致结合力的变化.     

Specific cancer stem cell-therapy by albumin nanoparticles functionalized with CD44-mediated targeting

Background

Cancer stem cells (CSCs) are highly proliferative and tumorigenic, which contributes to chemotherapy resistance and tumor occurrence. CSCs specific therapy may achieve excellent therapeutic effects, especially to the drug-resistant tumors.

Results

In this study, we developed a kind of targeting nanoparticle system based on cationic albumin functionalized with hyaluronic acid (HA) to target the CD44 overexpressed CSCs. All-trans-retinoic acid (ATRA) was encapsulated in the nanoparticles with ultrahigh encapsulation efficiency (EE%) of 93% and loading content of 8.37%. TEM analysis showed the nanoparticles were spherical, uniform-sized and surrounded by a coating layer consists of HA. Four weeks of continuously measurements of size, PDI and EE% revealed the high stability of nanoparticles. Thanks to HA conjugation on the surface, the resultant nanoparticles (HA-eNPs) demonstrated high affinity and specific binding to CD44-enriched B16F10 cells. In vivo imaging revealed that HA-eNPs can targeted accumulate in tumor-bearing lung of mouse. The cytotoxicity tests illustrated that ATRA-laden HA-eNPs possessed better killing ability to B16F10 cells than free drug or normal nanoparticles in the same dose, indicating its good targeting property. Moreover, HA-eNPs/ATRA treatment decreased side population of B16F10 cells significantly in vitro. Finally, tumor growth was significantly inhibited by HA-eNPs/ATRA in lung metastasis tumor mice.

Conclusions

These results demonstrate that the HA functionalized albumin nanoparticles is an efficient system for targeted delivery of antitumor drugs to eliminate the CSCs.

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Biodegradation of lignin by <Emphasis Type="Italic">Pseudomonas</Emphasis> sp. Q18 and the characterization of a novel bacterial DyP-type peroxidase

Lignin valorization can be obtained through cleavage of selected bonds by microbial enzymes, in which lignin is segregated from cellulose and hemicellulose and abundant phenolic compounds can be provided. In this study, Pseudomonas sp. Q18, previously isolated from rotten wood in China, was used to degrade alkali lignin and raw lignocellulosic material. Gel-permeation chromatography, field-emission scanning electron microscope, and GC–MS were combined to investigate the degradation process. The GC–MS results revealed that the quantities of aromatic compounds with phenol ring from lignin increased significantly after incubation with Pseudomonas sp. Q18, which indicated the degradation of lignin. According to the lignin-derived metabolite analysis, it was proposed that a DyP-type peroxidase (PmDyP) might exist in strain Q18. Thereafter, the gene of PmDyP was cloned and expressed, after which the recombinant PmDyP was purified and the enzymatic kinetics of PmDyP were assayed. According to results, PmDyP showed promising characteristics for lignocellulosic biodegradation in biorefinery.