Cyclohexanones

环己酮
  • 文章类型: Journal Article
    背景:氧化还原酶的大规模生物催化应用需要用于氧化还原辅因子的成本有效且有效的再生的系统。这些是工业生物生产的主要瓶颈和重要的成本因素。在这项工作中,来自伯克霍尔德氏菌的转化酶和Baeyer-Villiger单加氧酶基因共表达到大肠杆菌WΔcscR和大肠杆菌BL21(DE3),使环己酮有效地生物转化为聚合物前体,使用蔗糖作为氧化还原辅因子再生的电子源的ε-己内酯,速率与葡萄糖相当。大肠杆菌WΔcscR具有能够利用蔗糖的天然csc调节子,并且通过抑制基因(cscR)的缺失而失调,因此,即使在浓度低于6mM(2gL-1)时也能吸收蔗糖。另一方面,大肠杆菌BL21(DE3),它被广泛用作表达宿主,不包含csc调节子。
    结果:这里,我们展示了一个概念的证明,其中两个大肠杆菌宿主的转化酶共表达足以有效利用蔗糖以维持环己酮的Baeyer-Villiger氧化中的辅因子再生。使用大肠杆菌WΔcscR,获得了37UgDCW-1的比活性,证明该菌株适用于重组基因共表达和随后的全细胞生物转化。此外,将相同的共表达盒转移并用大肠杆菌BL21(DE3)进行研究,显示17UgDCW-1的比活性。最后,使用来自集胞藻S02的光合作用来源的蔗糖与表达BVMO的大肠杆菌WΔcscR的生物转化在3小时后显示环己酮的完全转化,特别是在周质中表达转化酶基因的菌株。
    结论:结果表明,蔗糖可以作为驱动重组大肠杆菌菌株全细胞生物转化的替代电子源,为可持续化学生产开辟了新的策略。
    BACKGROUND: The large-scale biocatalytic application of oxidoreductases requires systems for a cost-effective and efficient regeneration of redox cofactors. These represent the major bottleneck for industrial bioproduction and an important cost factor. In this work, co-expression of the genes of invertase and a Baeyer-Villiger monooxygenase from Burkholderia xenovorans to E. coli W ΔcscR and E. coli BL21 (DE3) enabled efficient biotransformation of cyclohexanone to the polymer precursor, ε-caprolactone using sucrose as electron source for regeneration of redox cofactors, at rates comparable to glucose. E. coli W ΔcscR has a native csc regulon enabling sucrose utilization and is deregulated via deletion of the repressor gene (cscR), thus enabling sucrose uptake even at concentrations below 6 mM (2 g L-1). On the other hand, E. coli BL21 (DE3), which is widely used as an expression host does not contain a csc regulon.
    RESULTS: Herein, we show a proof of concept where the co-expression of invertase for both E. coli hosts was sufficient for efficient sucrose utilization to sustain cofactor regeneration in the Baeyer-Villiger oxidation of cyclohexanone. Using E. coli W ΔcscR, a specific activity of 37 U gDCW-1 was obtained, demonstrating the suitability of the strain for recombinant gene co-expression and subsequent whole-cell biotransformation. In addition, the same co-expression cassette was transferred and investigated with E. coli BL21 (DE3), which showed a specific activity of 17 U gDCW- 1. Finally, biotransformation using photosynthetically-derived sucrose from Synechocystis S02 with E. coli W ΔcscR expressing BVMO showed complete conversion of cyclohexanone after 3 h, especially with the strain expressing the invertase gene in the periplasm.
    CONCLUSIONS: Results show that sucrose can be an alternative electron source to drive whole-cell biotransformations in recombinant E. coli strains opening novel strategies for sustainable chemical production.
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  • 文章类型: Journal Article
    这篇综述描述了新的有机催化方法,用于对映选择性构建螺茚坦和螺色满,以及这些方法在天然产物全合成中的应用。我们开发了分子内Friedel-Craftstype1,4-加成,其中底物是间苯二酚衍生物和通过烷基链连接的2-环己烯酮。在基于辛可尼丁的伯胺(30mol%)的存在下,以水和对溴苯酚为添加剂,反应顺利进行。在这些条件下获得了具有高对映选择性的各种螺环茚烷。该反应用于首次完全合成不寻常的原吗啡生物碱(-)-米拉胺,其中包括对映选择性螺环化和酮醛的双还原胺化的关键步骤,以在合成结束时形成哌啶环。米雷米汀的全合成是通过将前体中的甲氧基选择性去甲基化成米拉胺来实现的。接下来,开发了一种包含四取代立体中心的螺色满的高对映选择性有机催化构建方法。分子内氧-迈克尔加成是由双功能金鸡纳生物碱硫脲催化剂催化的。获得了多种包含四取代立体中心的螺色满化合物,其对映体选择性最高可达99%对映体过量。将该反应应用于(-)-(R)-Cordiachromene的不对称形式合成。
    This review describes novel organocatalytic methods for the enantioselective construction of spiroindans and spirochromans and the application of the methods to the total synthesis of natural products. We developed an intramolecular Friedel-Craftstype 1,4-addition in which the substrates were a resorcinol derivative and 2-cyclohexenone linked by an alkyl chain. The reaction proceeded smoothly in the presence of a cinchonidine-based primary amine (30 mol%) with water and p-bromophenol as additives. A variety of spiroindanes were obtained with high enantioselectivity under these conditions. The reaction was applied in the first total synthesis of the unusual proaporphine alkaloid (-)-misramine, which included the key steps of enantioselective spirocyclization and double reductive amination of the keto-aldehyde to form a piperidine ring toward the end of the synthesis. The total synthesis of misrametine was achieved by selective demethylation of the methoxy group from the precursor to misramine. Next, a method for highly enantioselective organocatalytic construction of spirochromans containing a tetrasubstituted stereocenter was developed. An intramolecular oxy-Michael addition was catalyzed by a bifunctional cinchona alkaloid thiourea catalyst. A variety of spirochroman compounds containing a tetrasubstituted stereocenter were obtained with excellent enantioselectivity of up to 99% enantiomeric excess. The reaction was applied to the asymmetric formal synthesis of (-)-(R)-cordiachromene.
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  • 文章类型: Journal Article
    具有人源化肝脏的嵌合小鼠模型(Hu-HEP小鼠)提供了研究人类嗜肝病毒疾病的独特工具,包括病毒感染,病毒发病机理,和抗病毒治疗。这里,我们描述了在NRG衍生的富马酸乙酰乙酸水解酶(FAH)敲除小鼠中研究乙型肝炎感染的详细方案与人肝细胞(FRG-HuHEP小鼠)。该程序包括(1)FRG小鼠的维持和基因分型,(2)脾内注射原代人肝细胞(PHH),(3)2-(2-硝基-4-氟甲基苯甲酰基)-1,3-环己二酮(NTBC)药物减少循环以改善人肝细胞再增殖,(4)人血白蛋白检测,(5)HBV感染和检测。该方法是简单的,并允许高重现的FRG-HuHEP小鼠的HBV感染和治疗研究的产生。
    Chimeric mouse models with a humanized liver (Hu-HEP mice) provide a unique tool to study human hepatotropic virus diseases, including viral infection, viral pathogenesis, and anti-viral therapy. Here, we describe a detailed protocol for studying hepatitis B infection in NRG-derived fumarylacetoacetate hydrolase (FAH) knockout mice repopulated with human hepatocytes (FRG-Hu HEP mice). The procedures include (1) maintenance and genotyping of the FRG mice, (2) intrasplenic injection of primary human hepatocytes (PHH), (3) 2-(2-nitro-4-fluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC) drug reduction cycling to improve human hepatocyte repopulation, (4) human albumin detection, and (5) HBV infection and detection. The method is simple and allows for highly reproducible generation of FRG-Hu HEP mice for HBV infection and therapy investigations.
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  • 文章类型: Journal Article
    背景:淀粉样β(Aβ)斑块的形成是阿尔茨海默病(AD)的关键神经病理学标志之一。近红外(NIR)探针显示出体内和体外Aβ斑块成像的巨大潜力。基于二氰基异佛尔酮(DCIP)的Aβ探针由于其优异的性质而吸引了相当多的关注。然而,DCIP探头仍然有一些缺点,例如短发射波长(<650nm)和与Aβ结合后的低荧光强度。显然,需要进一步的修饰以提高它们的发光效率和灵敏度。
    结果:我们设计并合成了四种新型吡咯烷-烷基氨基取代的DCIP衍生物(6a-d),作为β-淀粉样蛋白(Aβ)聚集体的显像剂。化合物6c对Aβ聚集体的响应比其他三种化合物更好(6a,6b和6d)及其前体DCIP。计算的检测极限低至0.23μM。对于SH-SY5Y和HL-7702细胞,化合物6c在测试浓度下没有显示细胞毒性。此外,化合物6c被成功地应用于监测活的SH-SY5Y细胞和APP/PS1转基因小鼠中的Aβ聚集体。转基因小鼠脑中的保留时间比年龄匹配的野生型小鼠长得多。
    结论:结果表明,化合物6c具有良好的穿透血脑屏障的能力,能有效区分APP/PS1转基因小鼠和宽型小鼠。这代表了其在基础和生物医学研究中用于Aβ检测的有希望的应用。
    BACKGROUND: The formation of amyloid-β (Aβ) plaques is one of the key neuropathological hallmarks of Alzheimer\'s disease (AD). Near-infrared (NIR) probes show great potential for imaging of Aβ plaques in vivo and in vitro. Dicyanoisophorone (DCIP) based Aβ probes have attracted considerable attention due to their exceptional properties. However, DCIP probes still has some drawbacks, such as short emission wavelength (<650 nm) and low fluorescence intensity after binding to Aβ. It is clear that further modification is needed to improve their luminescence efficiency and sensitivity.
    RESULTS: We designed and synthesize four novel pyrrolidine-alkylamino-substituted DCIP derivatives (6a-d) as imaging agents for β-amyloid (Aβ) aggregates. Compound 6c responds better to Aβ aggregates than the other three compounds (6a, 6b and 6d) and its precursor DCIP. The calculated detection limit is to be as low as 0.23 μM. Compound 6c shows no cytotoxicity in the tested concentration for SH-SY5Y and HL-7702 cells. Additionally, compound 6c is successfully applied to monitor Aβ aggregates in live SH-SY5Y cells and APP/PS1 transgenic mice. The retention time in the transgenic mice brain is much longer than that of age-matched wild-type mice.
    CONCLUSIONS: The results indicates that compound 6c had an excellent ability to penetrate the blood-brain barrier and it could effectively distinguish APP/PS1 transgenic mice and wide-type mice. This represents its promising applications for Aβ detection in basic and biomedical research.
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  • 文章类型: Journal Article
    BACKGROUND: Tyrosinaemia type I is a rare hereditary metabolic disease caused by deficiency of the enzyme involved in the breakdown of tyrosine. Since the use of nitisinone in addition to diet in 1992, survival rates have increased significantly, but more and more socio-emotional problems have become apparent. The aim of the study was the assessment the relationship between variations in serum tyrosine and phenylalanine levels and measurements of socio-emotional functioning and determination of patients\' IQs.
    OBJECTIVE: was the assessment the relationship between variations in serum tyrosine and phenylalanine levels and measurements of socio-emotional functioning and determination of patients\' IQs.
    METHODS: Twelve children were studied, from a single centre, born between 1994 and 2012, treated with nitisinone and a low-phenylalanine and -tyrosine diet. The psychological evaluation was conducted using the parent form of the Child Behaviour Checklist (CBCL)/4-18. Additionally, the patients\' IQs were measured using the Stanford-Binet 5 (SB5) Intelligence Scale. Statistical analyses were performed using PAWS software suite version 26. We found that phenylalanine variability over time correlated with measures of emotional and behavioural functioning. This relationship holds true for externalising behaviour, associated with the experience of maladjustment and aggression. Total score intellectual and cognitive function was within the norm for all patients.
    CONCLUSIONS: To maintain better quality of life for patients and their families in terms of emotional and behavioural functioning, it may be important to avoid spikes (significant fluctuations) in phenylalanine levels. Regular, detailed psychological evaluations are recommended to detect potential problems and implement interventions aimed at achieving the best possible individual development and realise the intellectual and behavioural potential, thereby improving the patient\'s and her family\'s quality of life.
    UNASSIGNED: Tyrozynemia typu 1 (TT1) to rzadka wrodzona choroba metaboliczna spowodowana deficytem enzymu biorącego udział w przemianie tyrozyny. Odkąd w 1992 r. w leczeniu oprócz diety zastosowano nityzynon, rokowanie co do przeżycia diametralnie się poprawiło, jednak coraz częściej zaczęto dostrzegać problemy społeczno-emocjonalne oraz zastanawiać się nad przyczynami ich występowania.
    UNASSIGNED: Określenie związku między zmiennością w stężeniach tyrozyny i fenyloalaniny w surowicy ze wskaźnikami funkcjonowania społeczno-emocjonalnego oraz ocena IQ pacjentów.
    UNASSIGNED: Badaniem objętych było 12 dzieci z Kliniki Pediatrii, Żywienia i Chorób Metabolicznych IP CZD urodzonych w latach 1994–2012, leczonych nityzynonem oraz dietetycznie. Badanie psychologiczne przeprowadzono przy użyciu Kwestionariusza Child Behavioral Checklist CBCL/4–18 w wersji dla rodziców. IQ u pacjentów określano za pomocą Skali Inteligencji Stanford-Binet 5 (SB5). Do analizy danych zastosowano pakiet statystyczny PASW wersja 26.
    UNASSIGNED: Stwierdzono, że zmienność czasowa fenyloalaniny koreluje ze wskaźnikami funkcjonowania emocjonalno-behawioralnego. Związek ten dotyczy grupy zachowań eksternalizacyjnych, związanych z przeżywaniem niedostosowania oraz agresji. Zdolności intelektualne i poznawcze na poziomie wyniku ogólnego u wszystkich badanych pacjentów mieszczą się w granicach normy.
    UNASSIGNED: W leczeniu TT1, w celu zachowania lepszego komfortu osób badanych oraz ich rodzin w wymiarze funkcjonowania emocjonalno-behawioralnego, istotne może być unikanie skoków (dużych wahań) w stężeniu fenyloalaniny. Wskazane jest systematyczne, szczegółowe badanie psychologiczne, aby jak najwcześniej uchwycić występujące problemy i wdrożyć interwencję terapeutyczną, aby uzyskać najlepszy z możliwych indywidualny rozwój i najlepiej wykorzystać potencjał intelektualny i behawioralny, a tym samym zwiększyć jakość życia pacjenta oraz jego rodziny.
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  • 文章类型: Journal Article
    生理参数,如生长,Chla内容,估计了实验蓝藻龙葵的光合性能HKAR-22,以评估光合有效辐射(PAR)和紫外线(UV)辐射的累积效应。紫外线屏蔽分子的最大诱导,MAAs,在PAR+UV-A+UV-B(PAB)辐射处理条件下观察到。UV/VIS吸收光谱和HPLC-PDA检测主要证实了在332.3nm处具有最大吸收(λmax)和1.47分钟的保留时间(RT)的MAA-shinorine(SN)的存在。为了进一步验证SN的存在,HRMS,利用FTIR和NMR。紫外线胁迫提高了体内ROS清除和体外酶促抗氧化能力。SN表现出实质性和浓度依赖性的抗氧化能力,这是利用2,2-二苯基-1-吡啶-肼基(DPPH)确定的,2,2'-嗪双-(3-乙基苯并噻唑啉-6-磺酸盐(ABTS),铁还原力(FRAP)和超氧自由基清除试验(SRSA)。使用B3LYP能量模型和6-311G++(d,p)暗示了基集进行量子化学计算,以系统地研究SN的抗氧化性质。还研究了抗氧化反应中涉及的主要途径以及影响化合物抗氧化潜力的基本分子描述符。结果有利于SN作为用于药妆制剂的活性成分的潜力。
    The physiological parameters such as growth, Chl a content, and photosynthetic performance of the experimental cyanobacterium Anabaenopsis circularis HKAR-22 were estimated to evaluate the cumulative effects of photosynthetically active radiation (PAR) and ultraviolet (UV) radiation. Maximum induction of UV-screening molecules, MAAs, was observed under the treatment condition of PAR + UV-A + UV-B (PAB) radiations. UV/VIS absorption spectroscopy and HPLC-PDA detection primarily confirmed the presence of MAA-shinorine (SN) having absorption maxima (λmax) at 332.3 nm and retention time (RT) of 1.47 min. For further validation of the presence of SN, HRMS, FTIR and NMR were utilized. UV-stress elevated the in vivo ROS scavenging and in vitro enzymatic antioxidant capabilities. SN exhibited substantial and concentration-dependent antioxidant capabilities which was determined utilizing 2,2-diphenyl-1-picryl-hydrazyl (DPPH), 2,2\'-azinobis-(3-ethylbenzothiazoline-6-sulfonate (ABTS), ferric reducing power (FRAP) and superoxide radical scavenging assay (SRSA). The density functional theory (DFT) method using B3LYP energy model and 6-311G++(d,p) basis set was implied to perform the quantum chemical calculation to systematically investigate the antioxidant nature of SN. The principal pathways involved in the antioxidant reactions along with the basic molecular descriptors affecting the antioxidant potentials of a compound were also studied. The results favor the potential of SN as an active ingredient to be used in cosmeceutical formulations.
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  • 文章类型: Journal Article
    转移性乳腺癌的骨转移通常由于破骨细胞活性而导致溶骨性病变,促进骨破坏和肿瘤进展。生物活性真菌分离株,4-乙酰基-蒽醌醇B(4-AAQB)和赤霉素A,具有多种药理和生物活性。然而,它们对乳腺癌骨转移治疗的影响尚不清楚.我们的研究旨在研究4-AQB或赤霉素A对乳腺癌骨转移的影响。4-AQB和赤霉素A对乳腺癌诱导的破骨细胞生成的影响,乳腺癌迁移,促转移细胞因子(TGF-β)和标志物(MMP-9)的产生,以及潜在的MAPK信号转导进行了评估。结果表明,4-AAQB和赤霉素A可有效抑制乳腺癌诱导的破骨细胞生成和迁移,并通过Erk或JNK信号转导减少TGF-β和MMP-9的产生,特别是在乳腺癌细胞或乳腺癌细胞诱导的破骨细胞中。基于这些发现,4-AQB或赤霉素A在预防乳腺癌骨转移方面显示出希望。
    Bone metastasis in metastatic breast cancer commonly results in osteolytic lesions due to osteoclast activity, promoting bone destruction and tumor progression. The bioactive fungal isolates, 4-acetyl-antroquinonol B (4-AAQB) and erinacine A, have diverse pharmacological and biological activities. However, their effects on breast cancer bone metastasis treatment remain unclear. Our study aimed to examine the impact of 4-AAQB or erinacine A on breast cancer metastases in bone. The effects of 4-AAQB and erinacine A on breast cancer-induced osteoclastogenesis, breast cancer migration, production of prometastatic cytokine (TGF-β) and marker (MMP-9), as well as potential MAPK signaling transductions were assessed. The results revealed that 4-AAQB and erinacine A effectively suppressed breast cancer-induced osteoclastogenesis and migration, and reduced TGF-β and MMP-9 production via Erk or JNK signaling transductions, specifically in breast cancer cells or in breast cancer cells-induced osteoclasts. Based on these findings, either 4-AAQB or erinacine A showed promise in preventing breast cancer metastases in bone.
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  • 文章类型: Journal Article
    甲基磺草酮是一种用于农业生产的除草剂;然而,其稳定性和长期残留对土壤健康和后续作物构成生态风险。在这项研究中,菌株AmycolatopsisniveaLa24被鉴定为能够在48小时内完全降解50mg·L-1甲基磺胺草酮。它对各种环境表现出广泛的适应性,并且可以降解三种磺酰脲类除草剂(烟磺隆,甲基氯胺隆,和西诺磺隆)。非目标代谢组学和质谱表明,La24菌株通过靶向β-二酮键和硝基基团来分解甲基磺草酮母体分子,导致产生五种可能的降解产物。差异表达基因在脂肪酸降解中显著富集,氨基酸代谢,和其他途径,和谷胱甘肽代谢中的差异代谢物,精氨酸/脯氨酸代谢,半胱氨酸/蛋氨酸代谢,和其他途径。此外,通过异源表达证实,硝基还原酶直接参与了甲基磺草酮的降解,NDMA依赖性甲醇脱氢酶会增加对甲基磺草酮的抗性。最后,提出了La24在甲基磺草酮降解过程中的细胞内反应。这项工作为全面了解甲基磺草酮生物降解机理提供了见解,大大扩大了污染物降解的资源,并提供了更可持续的解决方案来解决土壤中的除草剂污染的潜力。
    Mesotrione is a herbicide used in agricultural production; however, its stability and long-term residues pose ecological risks to soil health and subsequent crops. In this research, the strain Amycolatopsis nivea La24 was identified as capable of completely degrading 50 mg∙L-1 mesotrione within 48 h. It exhibited a broad adaptability to various environment and could degrade three sulfonylurea herbicides (nicosulfuron, chlorimuron-methyl, and cinosulfuron). Non-target metabonomic and mass spectrometry demonstrated that La24 strain broke down the mesotrione parent molecule by targeting the β-diketone bond and nitro group, resulting in the production of five possible degradation products. The differentially expressed genes were significantly enriched in fatty acid degradation, amino acid metabolism, and other pathways, and the differentially metabolites in glutathione metabolism, arginine/proline metabolism, cysteine/methionine metabolism, and other pathways. Additionally, it was confirmed by heterologous expression that nitroreductase was directly involved in the mesotrione degradation, and NDMA-dependent methanol dehydrogenase would increase the resistance to mesotrione. Finally, the intracellular response of La24 during mesotrione degradation was proposed. This work provides insight for a comprehensive understanding of the mesotrione biodegradation mechanism, significantly expands the resources for pollutant degradation, and offers the potential for a more sustainable solution to address herbicide pollution in soil.
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  • 文章类型: Journal Article
    Mesotrione,作为一种广泛使用的除草剂,以可检测的量存在于环境中,造成严重损害。这里,我们的目的是研究甲基磺草酮对Caco-2细胞的影响以及菊苣酸减轻其毒性的可能性。因此,我们分析了这两种化合物的细胞毒性和选定的氧化应激参数,两种测试化合物与细胞膜的凋亡和相互作用以及它们在细胞内的积累。在细胞毒性研究中,观察到甲基磺草酮的刺激活性,同时,观察到菊苣酸的抑制作用。这种作用与氧化应激分析和细胞凋亡测量的结果有关。关键酶(谷胱甘肽过氧化物酶,与对照相比,暴露于菊苣酸的Caco-2细胞中的过氧化氢酶和超氧化物歧化酶)更高。用甲基磺草酮处理不诱导Caco-2细胞的凋亡。通过使用HPLC方法测量研究的化合物向Caco-2细胞的渗透,结果表明甲基磺草酮具有较高的渗透能力。在两种化合物的影响下,细胞膜表面的电荷分布发生了变化。考虑到有益和潜在有毒食品成分的相互作用,应该指出的是,尽管观察到了有利的趋势,菊苣酸不能克服这种农药的毒性和癌症刺激作用。
    Mesotrione, as a widely used herbicide, is present in the environment in detectable amounts, causing serious damage. Here, we aimed to investigate the effect of mesotrione on Caco-2 cells and the possibility of its toxicity mitigation by cichoric acid. Therefore, we analyzed the cytotoxicity of both these compounds and the selected oxidative stress parameters, apoptosis and interaction of both the tested compounds with the cell membrane and their accumulation within the cells. In cytotoxicity studies, the stimulating activity of mesotrione was observed, and simultaneously, the inhibitory effect of cichoric acid was noticed. This effect was related to the results of oxidative stress analysis and apoptosis measurements. The activity level of key enzymes (glutathione peroxidase, catalase and superoxide dismutase) in Caco-2 cells exposed to cichoric acid was higher as compared to that of the control. The treatment with mesotrione did not induce apoptosis in the Caco-2 cells. The penetration of the studied compounds into the Caco-2 cells was measured by using an HPLC methodology, and the results indicate mesotrione\'s high penetration capacity. The distribution of charge on the surface of the cell membranes changed under the influence of both compounds. Considering the mutual interactions of beneficial and potentially toxic food ingredients, it should be noted that, despite the observed favorable trend, cichoric acid is not able to overcome the toxic and cancer-stimulating effects of this pesticide.
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  • 文章类型: Journal Article
    土壤和水中不需要的农用化学品残留物的存在对人类健康和环境都构成了风险。农药在土壤中的行为取决于农药的理化性质和土壤类型。这项研究检查了玉米除草剂tembotrione在上层(UGPZ)土壤中的吸附-解吸和浸出行为,跨(TGPZ)和印度中部恒河平原地区。使用丙酮提取土壤样品,然后用二氯甲烷分配,而使用二氯甲烷的液-液萃取用于水性样品。tembotrione及其代谢产物TCMBA的残留,{2-氯-4-(甲基磺酰基)-3-[(2,2,2-三氟乙氧基)甲基]苯甲酸},使用液相色谱-串联质谱法进行定量。数据显示,tembotrione吸附随pH和溶解有机物的增加而降低,但随盐度的增加而增加。最大吸附发生在pH4,0.01m柠檬酸钠和4g/LNaCl,相应的Freundlich常数分别为1.83、2.28和3.32。滞后指数<1表明吸附比解吸更快。在不同流动条件下的浸出研究表明,UGPZ土壤中的迁移率最小,而TGPZ土壤中的迁移率高。与地下水普遍性得分分别为4.27和4.81一致。土壤改良剂按以下顺序降低了tembotrione的迁移率:未改>小麦秸秆灰>小麦秸秆>农场肥料>堆肥。还评估了tembotrione向TCMBA的转化及其在土壤柱中的迁移率。
    The presence of undesired agrochemicals residues in soil and water poses risks to both human health and the environment. The behavior of pesticides in soil depends both on the physico-chemical properties of pesticides and soil type. This study examined the adsorption-desorption and leaching behavior of the maize herbicide tembotrione in soils of the upper (UGPZ), trans (TGPZ) and middle Gangetic plain zones of India. Soil samples were extracted using acetone followed by partitioning with dichloromethane, whereas liquid-liquid extraction using dichloromethane was used for aqueous samples. Residues of tembotrione and its metabolite TCMBA, {2-chloro-4-(methylsulfonyl)-3-[(2,2,2-trifluoroethoxy) methyl] benzoic acid}, were quantified using liquid chromatography-tandem mass spectrometry. The data revealed that tembotrione adsorption decreased with increasing pH and dissolved organic matter but increased with salinity. The maximum adsorption occurred at pH 4, 0.01 m sodium citrate and 4 g/L NaCl, with corresponding Freundlich constants of 1.83, 2.28 and 3.32, respectively. The hysteresis index <1 indicated faster adsorption than desorption. Leaching studies under different flow conditions revealed least mobility in UGPZ soil and high mobility in TGPZ soil, consistent with groundwater ubiquity scores of 4.27 and 4.81, respectively. Soil amendments decreased tembotrione mobility in the order: unamended > wheat straw ash > wheat straw > farm yard manure > compost. The transformation of tembotrione to TCMBA and its mobility in soil columns were also assessed.
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