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Exploring a Novel Metallophosphoesterase for Polycarbonate Degradation via Transcriptome Analysis 通过转录组分析探索聚碳酸酯降解的新型金属磷酸酯酶
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138330
Hyun-Woo Kim , Jieun Lee , Seongmin Kim , Seung-Do Yun , Ki Jung Kim , Min-Ju Seo , Hyeoncheol Francis Son , Dong-Jun Lee , Chungoo Park , Won Seok Chi , Soo-Jin Yeom
Polycarbonate (PC), a widely used thermoplastic, poses significant environmental challenges due to its persistence and the release of bisphenol A (BPA), a known xenoestrogen. Here, we report the isolation of Bacillus subtilis JNU01 (BsJNU01), capable of utilizing PC as its sole carbon source. Through transcriptomic analysis, we identified metallophosphoesterase from BsJNU01 (BsMPPE), the first reported metallophosphoesterase capable of degrading polycarbonate by catalyzing the hydrolysis of carbonate ester bonds. This enzyme operates under mild aqueous conditions (30 °C, pH 7), releasing 30 μmol of BPA as a monomer and demonstrating effective PC degradation under environmentally friendly conditions. PC biodegradation was confirmed by Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance (NMR), and gas chromatography-mass spectrometry (GC-MS). Furthermore, surface and mechanical analyses revealed significant degradation and structural changes in PC films following BsMPPE treatment, with toughness showing a 40–70 % decrease compared to untreated PC films. This study represents a breakthrough in microbial plastic degradation, establishing a sustainable biocatalytic platform for PC recycling and upcycling technologies.
聚碳酸酯(PC)是一种广泛使用的热塑性塑料,由于其持久性和双酚a(一种已知的雌性激素)的释放,对环境构成了重大挑战。在这里,我们报道了枯草芽孢杆菌JNU01 (BsJNU01)的分离,能够利用PC作为其唯一的碳源。通过转录组学分析,我们从BsJNU01 (BsMPPE)中鉴定出金属磷酸酯酶,这是第一个报道的能够通过催化碳酸酯酯键水解来降解聚碳酸酯的金属磷酸酯酶。该酶在温和的水环境(30°C, pH 7)下工作,以单体形式释放30 μmol的BPA,并在环境友好的条件下有效降解PC。通过傅里叶变换红外光谱(FT-IR)、核磁共振(NMR)和气相色谱-质谱(GC-MS)证实了PC的生物降解。此外,表面和力学分析显示,经过BsMPPE处理的PC膜有明显的降解和结构变化,与未处理的PC膜相比,韧性下降了40-70%。本研究代表了微生物塑料降解的突破,为PC回收和升级回收技术建立了可持续的生物催化平台。
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引用次数: 0
Sex-and stage-specific effect of prenatal exposure to organophosphate esters with children's physical growth patterns and adiposity rebound timing: Modification by breastfeeding 产前暴露于有机磷酸酯对儿童身体生长模式和肥胖反弹时间的性别和阶段特异性影响:通过母乳喂养修正
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138309
Xing Wang , Juan Tong , Han Li , Mengjuan Lu , Yuan Liu , Hong Gan , Yifan Wang , Menglong Geng , Xuejiao Qie , Xiulong Wu , Hui Gao , Beibei Zhu , Shuman Tao , Xingyong Tao , Shuangqin Yan , Guopeng Gao , Xiaoyan Wu , Kun Huang , Yunxia Cao , Fangbiao Tao

Introduction

Exploring the stage-specific effects of prenatal exposure to organophosphate esters (OPEs) on offspring growth and developmental trajectories is critical for early-life health management.

Methods

Based on 2519 mother-child dyads from the Ma'anshan Birth Cohort, we examined the concentrations of OPEs in maternal urine during the three trimesters. Seventeen follow-up visits were made to the children, and physical data were collected. A grouped trajectory model was used to fit the growth trajectories.

Results

First-trimester bis(2-butoxyethyl) phosphate (BBOEP) was inversely associated with the children's adiposity rebound (AR) timing (β = −0.33, 95 % CI: −0.65, −0.01), and the ORs (95 % CIs) for early age at AR for each doubling of BBOEP and dibutyl phosphate (DBP) were 1.07 (1.00, 1.14) and 1.12 (1.03, 1.22), respectively. BBOEP increased the risk of a high-stable BMI-for-age z score (BMIz) group (OR = 1.18, 95 % CI: 1.01, 1.39), whereas tris(2-chloroethyl) phosphate (TCEP) and bis(2-ethylhexyl) phosphate reduced this risk. Diphenyl phosphate (OR = 0.74, 95 % CI: 0.59, 0.94) and aromatic OPEs (OR = 0.70, 95 % CI: 0.54, 0.90) reduced the odds of an extreme-high body fat group. TCEP also reduced the risk of a high body fat percentage group (p < 0.05). There appeared to be sex and ester bond differences in these associations, and breastfeeding could counteract the association between the OPEs and growth trajectories. No mixed effects of OPEs on BMIz trajectories were found.

Conclusions

The present study identified a heterogeneous association between OPE exposure during pregnancy and AR timing and physical growth patterns in offspring. Future studies are needed involving more regions and populations, with consideration of other developmentally toxic compounds, to obtain more reliable and comprehensive results.
探讨产前暴露于有机磷酸酯(OPEs)对后代生长和发育轨迹的阶段特异性影响对早期生命健康管理至关重要。方法对来自马鞍山出生队列的2519对母子进行3个月的尿液OPEs浓度检测。对这些儿童进行了17次随访,并收集了身体数据。采用分组轨迹模型拟合生长轨迹。结果孕早期双(2-丁氧乙基)磷酸酯(BBOEP)与儿童肥胖反弹(AR)时间呈负相关(β = -0.33, 95% CI: -0.65, -0.01), BBOEP和磷酸二丁酯(DBP)每增加一倍的早期AR的or (95% CI)分别为1.07(1.00,1.14)和1.12(1.03,1.22)。BBOEP增加了高稳定年龄bmi - z评分(BMIz)组的风险(OR = 1.18, 95% CI: 1.01, 1.39),而三(2-氯乙基)磷酸(TCEP)和二(2-乙基己基)磷酸降低了这一风险。磷酸二苯酯(OR = 0.74, 95% CI: 0.59, 0.94)和芳香OPEs (OR = 0.70, 95% CI: 0.54, 0.90)降低了极高体脂组的几率。TCEP还降低了高体脂率组的风险(p <;0.05)。在这些联系中似乎存在性别和酯键的差异,母乳喂养可以抵消OPEs和生长轨迹之间的联系。没有发现OPEs对BMIz轨迹的混合影响。结论:本研究发现妊娠期间暴露于OPE与子代AR时间和身体生长模式之间存在异质性关联。未来的研究需要涉及更多的地区和人群,并考虑到其他发育毒性化合物,以获得更可靠和全面的结果。环氧乙烷作为常见的阻燃剂,已被证明会引起健康问题。怀孕期间接触这种物质不仅影响产妇健康,甚至可能危及后代的生长发育。因此,关注怀孕期间暴露于OPEs与后代生长之间的关系至关重要。我们的研究结果可能会呼吁更多的孕妇在怀孕期间进行自我保护,并提供母乳喂养作为干预措施,以改善环境引起的危害,为后代创造良好的生长环境。本研究也为未来的公共卫生政策制定提供了依据,并为未来的研究提供了新的视角。
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引用次数: 0
Rapid detection of microplastics and nanoplastics in seconds by mass spectrometry 质谱法快速检测微塑料和纳米塑料
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138322
Mengyuan Xiao , Yongqing Yang , Hanin Alahmadi , Allison Harbolic , Gina M. Moreno , Terry Yu , Jerry Liu , Alex Guo , Genoa R. Warner , Phoebe A. Stapleton , Hao Chen
Microplastics (MPs) and nanoplastics (NPs) are pervasive pollutants and their analyses by traditional mass spectrometric methods require time-intensive sample preparation (e.g., extraction, digestion, and separation). This study presents a rapid and novel method for detecting MPs and NPs using flame ionization mass spectrometry (FI-MS) in which a dried sample (e.g., powder, soil and tissue) is directly burnt or heated with a flame in front of the MS inlet. FI-MS enables decomposition and ionization of various plastics such as polyethylene terephthalate (PET) and polystyrene (PS), allowing for analysis to be completed as fast as 10 seconds per sample. As a demonstration of application of this technique, PET contaminants in 1 L of bottled water or in 0.65 L of apple juice contained in plastic bottles were quickly detected from a filter paper after sample filtration and brief drying. A 0.89 mg soil sample spiked with 6000 ppm PET microplastics was measured to contain 4.98 µg of PET (5595 ppm, quantitation error: 6.8 %). Strikingly, PS nanoplastics (200 nm size) in mouse placentas were successfully identified and quantified, highlighting the method's ability to analyze biological tissue without tedious sample preparation. Overall, this study demonstrates the high potential of FI-MS for real-world sample analysis of MPs and NPs in environmental, biological, or consumer product samples.
微塑料(MPs)和纳米塑料(NPs)是普遍存在的污染物,用传统的质谱方法分析它们需要耗费大量时间进行样品制备(如提取、消化和分离)。本研究提出了一种利用火焰离子化质谱(FI-MS)快速检测 MPs 和 NPs 的新方法,即将干燥样品(如粉末、土壤和组织)直接在质谱入口前用火焰燃烧或加热。FI-MS 可使聚对苯二甲酸乙二醇酯(PET)和聚苯乙烯(PS)等各种塑料分解和离子化,每个样品的分析可在 10 秒钟内完成。作为该技术的应用示范,1 升瓶装水或 0.65 升塑料瓶装苹果汁中的 PET 污染物在经过水过滤和短暂干燥后,可从滤纸上快速检测出来。在 0.89 毫克土壤样品中添加 6,000 ppm PET 微塑料后,测得其中含有 4.98 微克 PET(5,595 ppm,定量误差:6.8%)。引人注目的是,小鼠胎盘中的 PS 纳米塑料(200 nm 大小)也被成功鉴定和定量,凸显了该方法无需繁琐的样品制备即可分析生物组织的能力。总之,这项研究证明了 FI-MS 在实际样品分析环境、生物或消费品样品中的 MPs 和 NPs 方面的巨大潜力。
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引用次数: 0
Differential effects of environmentally relevant concentrations of ibuprofen on denitrification and nitrous oxide emissions in river sediments 布洛芬环境相关浓度对河流沉积物反硝化和氧化亚氮排放的差异影响
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138326
Tongyue Zhuo , Sibo Zhang , Zhong Zhang, Yanpeng Cai
The increasing presence of ibuprofen in aquatic ecosystems poses significant challenges to their biogeochemical functions, including nitrogen transformations. In this study, we employed 15N-labeling techniques to investigate the effects of environmentally relevant concentrations of ibuprofen (0–10,000 ng L−1) on denitrification and the associated nitrous oxide (N2O) emissions in river sediments over a 60-day period. The results revealed a hump-shaped response in denitrification rates to ibuprofen addition across a range of nitrate concentrations (1–60 mg N L−1), with rates peaking near 200 ng L−1 ibuprofen, followed by inhibition at certain higher concentrations, leading to a reduction of up to 25.8 % compared to the treatment without ibuprofen. Kinetic analysis showed that the maximum denitrification rate followed the same hump-shaped trend, despite a decrease in nitrate affinity with increasing ibuprofen concentrations. The abundance of denitrifying bacteria mirrored the pattern observed in denitrification rates across different ibuprofen concentrations. However, increasing ibuprofen concentrations consistently accelerated N2O production rates. Microbial analysis suggests that the increase in N2O production genes was faster than for reduction genes, while the decrease was slower with increasing ibuprofen concentrations. This study highlights the hump-shaped response of denitrification rates and the consistent increase in N2O emissions induced by ibuprofen, offering insights for developing environmental management strategies to mitigate ibuprofen and nitrogen pollution, as well as reducing N2O emissions.
布洛芬在水生生态系统中日益增加的存在对其生物地球化学功能(包括氮转化)构成了重大挑战。在这项研究中,我们采用15n标记技术研究了环境相关浓度的布洛芬(0-10,000 ng L-1)在60天内对河流沉积物中反硝化和相关氧化亚氮(N2O)排放的影响。结果显示,在硝酸盐浓度范围内(1-60 mg N - L-1),添加布洛芬对脱氮速率有驼峰状响应,在200 ng L-1布洛芬附近速率达到峰值,随后在某些较高浓度下受到抑制,与不添加布洛芬的处理相比,脱氮速率降低了25.8%。动力学分析表明,随着布洛芬浓度的增加,硝酸盐亲和力降低,但最大反硝化速率呈相同的驼峰型趋势。反硝化细菌的丰度反映了不同布洛芬浓度下反硝化率的变化规律。然而,增加布洛芬浓度持续加速N2O的生成速率。微生物分析表明,N2O产生基因的增加速度快于还原基因,而随着布洛芬浓度的增加,N2O产生基因的减少速度较慢。该研究强调了布洛芬引起的反硝化速率的驼峰响应和N2O排放的持续增加,为制定环境管理策略以减轻布洛芬和氮污染以及减少N2O排放提供了见解。
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引用次数: 0
Plastic additives in the diet: Occurrence and dietary exposure in different population groups 饮食中的塑料添加剂:在不同人群中的发生和饮食暴露
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138317
Julio Fernández-Arribas, Teresa Moreno, Ethel Eljarrat
A total diet study focused on exposure to plastic additives has been performed on 109 food samples. Plasticizers were detected in 85 % of analyzed samples with total concentrations ranging between not detected (nd) and 22.0 µg/g wet weight (ww). Non-phthalate plasticizers (NPPs), such as acetyl tributyl citrate (ATBC) or di(2-ethylhexyl) adipate (DEHA), were detected predominantly in baby foods (nd-3.38 µg/g ww) and meat (nd-15.0 µg/g ww), respectively. Significant differences (p ≤ 0.001) were observed across foods with different packaging types regarding the presence of ATBC and DEHA. ATBC was primarily detected in foods packaged in glass containers, meanwhile DEHA is mainly related to fresh food wrapped in plastic materials. Additionally, transference assays in selected ready to cook meals and fresh vegetables were performed, with NPPs exhibiting a higher transference from packaging to food than other compounds. The data obtained have been used for an assessment of estimated daily intake (EDI) of plastic additives in infants (6–12 months), toddlers (1–3 years), and adults (>18 years), resulting in values ranging 0.29–516 µg/kg body weight (bw)/day. Human risk related to baby food consumption, expressed as hazard quotients (HQs), was found with di(2-ethylhexyl) phthalate (DEHP) in the infant population sub-group.
对109个食品样本进行了一项以塑料添加剂暴露为重点的全面饮食研究。85%的分析样品中检测到增塑剂,总浓度范围在未检测到(nd)和22.0µg/g湿重(ww)之间。非邻苯二甲酸酯增塑剂(NPPs),如乙酰柠檬酸三丁酯(ATBC)或己酸二(2-乙基己基)二(DEHA),主要在婴儿食品中检测到(nd-3.38µg/g ww)。肉(nd-15.0µg/g ww)。在不同包装类型的食品中观察到ATBC和DEHA存在显著差异(p≤0.001)。ATBC主要在玻璃包装的食品中检测到,DEHA主要在塑料包装的新鲜食品中检测到。此外,在选定的即食饭菜和新鲜蔬菜中进行了转移试验,与其他化合物相比,NPPs从包装到食物的转移率更高。所获得的数据已用于评估婴儿(6-12个月)、幼儿(1-3岁)和成人(18岁)塑料添加剂的估计每日摄入量(EDI),得出的数值范围为0.29-516µg/kg体重(bw)/天。与婴儿食品消费相关的人类风险,以危险商(hq)表示,在婴儿人群亚组中发现邻苯二甲酸二(2-乙基己基)酯(DEHP)。
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引用次数: 0
On-site tracking of trace Aflatoxin B1 in food waste composting via a portable colorimetric sensing platform with nanozymes 基于纳米酶的便携式比色传感平台对食物垃圾堆肥中痕量黄曲霉毒素B1的现场跟踪
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138333
Yating Lu , Fuqing He , Xu Zhu , Jing Tang , Yue Lu , Jiajia Wang , Jiangfang Yu , Li Chen , Xingyang Cheng , Tianhao Liu , Lin Tang
Rapid, on-site accurate tracking of harmful mycotoxin in food waste composting is essential to provide instant content information for efficient supervision. However, on-site analytical tools especially colorimetric sensors currently suffer from low sensitivity/selectivity and poor environment robustness, posing hurdles for their applications. In this work, we have proposed a portable paper-based colorimetric sensor to detect the representative mycotoxin (aflatoxin B1, AFB1) in the composting process, where the superior catalytic velocity (6-fold higher than the natural enzyme) and well-regulated catalytic activity of nanozyme by the aptamers ensure the high sensitivity (a wide linear range: 0.1–1000 ng/mL; an ultra-low limit of detection: 0.082 ng/mL) and good selectivity of the colorimetric sensing, respectively. The smartphone-based platform exhibits high accuracy with the relative standard deviation within 3.67 % compared commercial enzyme-linked immunosorbent assay. Finally, on-site tracking of the AFB1 content in food waste during the composting process with or without the oxidant (potassium persulfate) has been carried out using the developed colorimetric sensor. It is concluded that reducing the AFB1 generation in the food waste is more meaningful than the compost treatment. This study offers a promising method for in situ analysis of trace AFB1 in food waste compost to ensure environmental and human health safety.
快速,现场准确跟踪食物垃圾堆肥中的有害真菌毒素对于提供即时含量信息以进行有效监管至关重要。然而,现场分析工具特别是比色传感器目前存在灵敏度/选择性低和环境鲁棒性差的问题,给其应用带来了障碍。在这项工作中,我们提出了一种便携式纸基比色传感器,用于检测堆肥过程中的代表性真菌毒素(黄曲霉毒素B1, AFB1),其中适体具有比天然酶高6倍的催化速度和良好的调节纳米酶的催化活性,确保了高灵敏度(宽线性范围:0.1-1000 ng/mL;超低检出限:0.082 ng/mL),比色感应选择性好。与市售酶联免疫吸附法相比,基于智能手机的平台具有较高的准确性,相对标准偏差在3.67%以内。最后,利用开发的比色传感器对堆肥过程中食物垃圾中AFB1的含量进行了现场跟踪,无论是否添加氧化剂(过硫酸钾)。综上所述,减少食物垃圾中AFB1的产生比堆肥处理更有意义。本研究为食物垃圾堆肥中痕量AFB1的原位分析提供了一种有前景的方法,以确保环境和人类健康安全。
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引用次数: 0
Methodological guidance to the batch preparation of graphene-based sensor for low-cost and high-performance Cd2+ and Pb2+ detection 批量制备石墨烯基传感器的方法指导,用于低成本、高性能的 Cd2+ 和 Pb2+ 检测
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138331
Wenshuai Ye , Ning Liu , Sicheng Li , Guo Zhao , Gang Liu
The cost-effective, disposable, batch-prepared electrochemical sensors with high sensitivity and accurate detection are essential to the rapid on-site detection of heavy metals in soil and water. Here, we report a one-step laser additive manufacturing technique for the batch fabrication of electrochemical sensors. With the systematic optimization of multiple laser parameters (including laser power, engraving speed, and frequency), highly sensitive laser-induced porous graphene (LIPG) electrodes were fabricated to detect Cd2+ and Pb2+ efficiently. Followingly, with the modification of Nafion and bismuth-film, the obtained Bi/Nafion/LIPG electrode showed excellent repeatability, stability, selectivity, and outstanding detection limits of 0.25 µg/L for Cd2+ and 0.41 µg/L for Pb2+, respectively. As-prepared Bi/Nafion/LIPG electrode also works in actual soil and water samples, with an average recovery of 99.61 and 99.90 for Cd2+ and Pb2+. Furthermore, from the perspective of the laser photothermal effect, the important influence of laser parameters on the physical and chemical properties of LIPG was analyzed, confirming that the laser photothermal effect has a superimposed cumulative effect on the surface of the PI film. This study provides a new methodical guidance for the rapid and batch preparation of LIPG electrodes with the advantages of low-cost, disposable, high-sensitivity, and flexibility, which can promote the on-site electrochemical detection of heavy metals in soil and water.
高效、一次性、批量制备、灵敏度高、检测准确的电化学传感器对于土壤和水中重金属的快速现场检测至关重要。本文报道了一种用于批量制造电化学传感器的一步激光增材制造技术。通过对多个激光参数(包括激光功率、雕刻速度和频率)的系统优化,制备了高灵敏度的激光诱导多孔石墨烯(LIPG)电极,用于高效检测Cd2+和Pb2+。随后,通过对Nafion和铋膜的修饰,得到的Bi/Nafion/LIPG电极具有良好的重复性、稳定性和选择性,对Cd2+和Pb2+的检出限分别为0.25µg/L和0.41µg/L。制备的Bi/Nafion/LIPG电极也适用于实际土壤和水样,对Cd2+和Pb2+的平均回收率分别为99.61和99.90。进一步,从激光光热效应的角度分析了激光参数对LIPG物理化学性质的重要影响,证实了激光光热效应在PI膜表面具有叠加累积效应。本研究为快速批量制备具有低成本、一次性、高灵敏度、柔性等优点的LIPG电极提供了新的方法指导,可促进土壤和水中重金属的现场电化学检测。
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引用次数: 0
A CCT protein GmCIC5 activates GmP5CS to regulate proline accumulation and cadmium tolerance in vegetable soybean CCT蛋白GmCIC5激活GmP5CS调控菜用大豆脯氨酸积累和耐镉性
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138319
Bin Wang , Ruiqiu Fang , Guwen Zhang , Na Liu , Zhijuan Feng , Yuanpeng Bu , Yaming Gong
Cadmium (Cd) toxicity poses a severe environmental threat, leading to substantial declines in crop growth and productivity worldwide. Accumulation of proline is recognized as a critical adaptive response in plants facing heavy metal stress. However, the precise mechanisms regulating Cd-induced proline accumulation remain elusive. Here, we discovered that a Cd-induced CCT5 gene in vegetable soybean, designated as GmCIC5, plays a pivotal role in regulating proline biosynthesis by activating the transcription of the proline biosynthesis gene, GmP5CS. Under greenhouse conditions, silencing GmCIC5 plants exhibited heightened sensitivity to Cd stress and suppressed root growth after 15 days of 30 mg/L CdCl2 treatment. Furthermore, qRT-PCR and ChIP-qPCR revealed that GmCIC5 directly targeted GmP5CS. Consequently, the GmCIC5 knockdown plants showed drastically reduced levels of GmP5CS transcripts and proline accumulation. Overexpression of GmP5CS largely suppressed the Cd hypersensitivity phenotype of GmCIC5 knockdown plants, suggesting that GmCIC5-mediated Cd tolerance was dependent on proline. Taken together, our results indicated that GmCIC5 is a novel regulator of Cd stress tolerance through proline biosynthesis, which may provide new insights into the molecular mechanisms of plant responses to Cd stress and offer a theoretical foundation for breeding Cd-resistant crops.
镉(Cd)毒性造成了严重的环境威胁,导致全球作物生长和生产力大幅下降。脯氨酸的积累是植物在重金属胁迫下的重要适应性反应。然而,调节cd诱导脯氨酸积累的精确机制仍然难以捉摸。在这里,我们发现cd诱导的菜用大豆CCT5基因GmCIC5通过激活脯氨酸生物合成基因GmP5CS的转录,在调节脯氨酸生物合成中起关键作用。在温室条件下,30 mg/L CdCl2处理15 d后,沉默GmCIC5植株对Cd胁迫的敏感性提高,根系生长受到抑制。此外,qRT-PCR和ChIP - qPCR显示GmCIC5直接靶向GmP5CS。因此,GmCIC5基因敲除植株的GmP5CS转录本和脯氨酸积累水平显著降低。GmP5CS的过表达在很大程度上抑制了GmCIC5敲除植株的Cd超敏表型,表明GmCIC5介导的Cd耐受依赖于脯氨酸。综上所述,GmCIC5是一种通过脯氨酸生物合成调控Cd胁迫的新基因,这可能为植物对Cd胁迫响应的分子机制提供新的认识,并为选育抗Cd作物提供理论基础。
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引用次数: 0
Denitrification dominates nitrate attenuation and nitrous oxide effluxes under water table fluctuations 在地下水位波动下,反硝化作用主导硝酸盐衰减和氧化亚氮流出
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138325
Lin Zhang , Helin Wang , Xiaohan Liu , Hongbin Zhan , Uwe Schneidewind , Stefan Krause , Menggui Jin , Xing Liang , Yanfeng Liu , Ping Li
Agricultural soils in riparian zones near rivers often experience frequent water table fluctuations, which can lead to increased nitrogen losses and greenhouse gas emissions via the nitrogen biogeochemical processes. However, the influence of water table fluctuations on the multiple nitrogen transformation processes that dominate nitrate attenuation and nitrous oxide (N2O) effluxes remains poorly understood. In this study, the dynamic changes in depth-dependent nitrate attenuation and soil N2O effluxes, and the responses of microbial communities influenced by water table fluctuations were studied using a series of large column experiments. Our results revealed that dissolved oxygen (DO) concentrations at a depth of −10 cm in sand columns with three different grain sizes (fine→medium→coarse) oscillated, producing oxidizing conditions during drainage and reducing conditions during imbibition periods. DO micro-sensors installed in a layered (sand and sandy loam) column as well as in two sandy loam columns with different regimes in induced water table changes all revealed steady hypoxic conditions. The diversity of the microbial community was significantly correlated with total nitrogen, total organic carbon, and nitrate concentrations, as well as potential denitrification rates. The dominant microbial populations related to the nrfA gene were Methanothrix and Sedimentibacte, whereas those related to denitrification (nirK, nirS, and nosZ) were Pseudomonas and Sulfuricaulis. These findings improve our understanding of the effects of water table fluctuations on groundwater nitrate loss in riparian corridors.
靠近河流的河岸地带的农业土壤经常经历频繁的地下水位波动,这可能通过氮生物地球化学过程导致氮损失和温室气体排放增加。然而,地下水位波动对主导硝酸盐衰减和氧化亚氮(N2O)外排的多种氮转化过程的影响仍知之甚少。本研究采用大型柱形实验,研究了深度依赖的硝酸盐衰减和土壤N2O外排的动态变化,以及微生物群落对地下水位波动的响应。结果表明,3种不同粒度(细→中→粗)的砂柱在−10 cm深度处溶解氧(DO)浓度振荡,在排水期间产生氧化状态,在吸胀期间产生还原状态。安装在层状(砂和砂壤土)柱中的DO微传感器以及在诱导地下水位变化的不同制度下安装在两个砂壤土柱中的DO微传感器都显示出稳定的缺氧条件。微生物群落多样性与总氮、总有机碳、硝态氮浓度及潜在反硝化速率呈显著相关。与nrfA基因相关的优势菌群为Methanothrix和Sedimentibacte,与反硝化相关的优势菌群(nirK、nirS和nosZ)为Pseudomonas和sulphicaulis。这些发现提高了我们对地下水位波动对河岸走廊地下水硝酸盐损失的影响的理解。
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引用次数: 0
Persistent free radicals in the environment 环境中持久的自由基
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-04-17 DOI: 10.1016/j.jhazmat.2025.138332
Linjun Qin , Wuyuxin Zhu , Lili Yang , Minghui Zheng , Guorui Liu
Environmentally persistent free radicals (EPFRs) are environmental pollutants whose potential DNA damage and apoptosis toxicity may be mediated by reactive oxygen species (ROS). The currently available knowledge of their environmental characteristics and transformation mechanisms is not sufficient to understand the environmental behaviors and health effects of EPFRs and should be further expanded. This review offers a comprehensive review of the current state of EPFRs, including characterization methods, formation mechanisms, and environmental behavior of EPFRs. Electron paramagnetic resonance (EPR) spectroscopy directly probes EPFRs in environmental matrices. EPFRs can be simply categorized by g value, but structure confirmation solely by EPR is challenging because the complexity of environmental matrices results in the absence of a hyperfine splitting spectrum. Combined advanced EPR and multi-spectroscopic methods enable the structural identification of EPFRs in environmental samples. The environmental behavior and ecological impacts of EPFRs have been progressively studied. This review highlights the important role of EPFRs in natural environments and emphasizes the necessity of further research on EPFRs.
环境持久性自由基(environmental persistent free radicals, EPFRs)是一种环境污染物,其潜在的DNA损伤和细胞凋亡毒性可能由活性氧(reactive oxygen species, ROS)介导。目前对其环境特征和转化机制的现有知识不足以了解epfr的环境行为和健康影响,应进一步扩大。本文综述了epfr的研究现状,包括epfr的表征方法、形成机制和环境行为。电子顺磁共振(EPR)光谱直接探测环境基质中的epfr。epfr可以通过g值简单地分类,但仅通过EPR来确认结构是具有挑战性的,因为环境矩阵的复杂性导致缺乏超精细分裂光谱。结合先进的EPR和多光谱方法,可以对环境样品中的epfr进行结构鉴定。epfr的环境行为和生态影响的研究日益深入。本文综述了epfr在自然环境中的重要作用,并强调了进一步研究epfr的必要性。
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引用次数: 0
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Journal of Hazardous Materials
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