农药酶免疫分析技术研究进展

自从酶免疫分析原理提出后，近30年来已获得了巨大的进步，成为农药分析的一个非常重要的方法。本文对农药酶免疫分析技术的原理和测定程序进行了评述．并总结了近年酶免疫分析在农药领域研究中的应用，最后，对农药酶免疫分析技术存在的问题和发展趋势作了讨论。     

Gly-Gly肽和Gly-L-Leu肽在蛋鸡肠道内水解的研究

采用蛋鸡离体外翻肠段培养法,将小肠分为十二指肠、空肠前段、中段、后段和回肠五个部位肠段,洗净外翻。2种二肽培养液(Gly-Gly肽和Gly-L-Leu肽溶液)作为两组对照培养液,每种二肽培养液中添加肽酶抑制剂(Bestatin和Amastatin),作为试验培养液,39.5℃培养25min,每5min取样一次,测定培养液中的二肽含量。结果表明,培养5min后,含Gly-Gly肽的对照和试验培养液中均未能检测到完整Gly-Gly肽。而含Gly-L-Leu肽的对照培养液Gly-L-Leu肽的含量降低到16.75％,试验培养液则下降到43.40％。而试验培养液中Gly-L-Leu肽的含量10min后无显著降低(P>0.05)。各培养时段试验培养液Gly-L-Leu含量均显著高于对照培养液(P<0.05)。由此认为,离体肠囊在培养过程中能够迅速释放肠肽酶及一些生物活性物质,快速水解2种二肽。肽酶抑制剂(Bestatin和Amastatin)能抑制Gly-L-Leu的水解,但不能抑制Gly-Gly的水解。     

活化铁尾砂与镁改性生物炭配施对水稻幼苗生长及盐碱土性质的影响

为探究活化的高硅型铁尾砂与镁改性生物炭配施材料对水稻幼苗生长及盐碱土壤理化性质的影响以及改善盐碱地水稻生产力的可行性,本研究应用电子扫描显微镜对生物炭材料进行形貌结构观察,应用傅里叶变换红外光谱仪对生物炭材料进行官能团表征;开展盆栽实验,探究活化铁尾砂与生物炭材料配施对水稻幼苗的形态学和生理学的影响及对盐碱土的改善效果。结果表明,相比于其他生物炭材料,活化铁尾砂-镁改性生物炭材料孔隙较大,表面更加粗糙,对于养分的吸附能力强,表面的官能团丰富。盆栽实验中活化铁尾砂-镁改性生物炭配施组中水稻幼苗株高、根长、根冠比和干质量分别较对照组提高12.61%、191.49%、42.93%和100.00%;叶片的丙二醛和活性氧含量分别降低65.76%和46.46%;过氧化氢酶、超氧化物歧化酶、叶绿素和可溶性蛋白值分别升高117.35%、44.75%、55.00%和19.31%。施用活化铁尾砂-镁改性生物炭材料后,盐碱土的电导率降低,p H、总碳、总氮、土壤有效硅、总磷和总钾含量升高。研究证明活化铁尾砂-镁改性生物炭材料性能优越,并且活化铁尾砂与镁改性生物炭配施改善了盐碱土壤理化性质和养分含量,使水稻幼...     

微塑料对双酚A在鲤鱼肠道中累积及生长生理的影响

探明微塑料（MPs）对双酚A （BPA）在鱼类肠道中累积特征及鱼类生长生理的影响,本研究以黄河鲤鱼为模型生物,分析了0.5 μm聚苯乙烯微塑料（PS-MPs）与BPA联合作用下鲤鱼肠道中微塑料及BPA的累积特征、鲤鱼生长及其抗氧化酶活性,以及它们之间的响应关系。结果表明：联合处理下鲤鱼肠道中的PS-MPs含量随时间呈线性增加,且随投加的微塑料浓度增加而增加,而PS-MPs累积速率随时间呈先增加后减小趋势,其中在BPA+PS（L）处理（1 mg·L^-1 BPA+20 μg·L^-1 PS-MPs）下,0.25 d时鲤鱼肠道中PS-MPs累积速率达到峰值（373.81 μg·g^-1·d^-1）,BPA+PS（H）处理（1 mg·L^-1 BPA+100 μg·L^-1 PS-MPs）下,则是在0.125 d达到最高（644.00 μg·g^-1·d^-1）。与单一BPA暴露相比,联合暴露下鲤鱼肠道中BPA累积量增加,与BPA （1 mg·L^-1 BPA）处理相比,BPA+PS （L）和BPA+PS （H）处理下鲤鱼肠道中BPA含量分别提高了6.13%和9.74%,BPA累积速率分别增加了190.01%、373.80%。相较于对照处理,BPA处理和MPs与BPA联合处理均引起鲤鱼肠组织中超氧化物歧化酶（SOD）活性、过氧化氢酶（CAT）活性、还原型谷胱甘肽（GSH）含量、丙二醛（MDA）含量增加,使体质量下降幅度减缓,其中BPA、BPA+PS （L）和BPA+PS （H）处理下鲤鱼体质量（21 d）较对照处理分别下降1.22%、3.90%、4.33%。当微塑料投加量达到100 μg·mL^-1时,联合处理会增加鲤鱼肠道中SOD活性、CAT活性和GSH含量,抑制MDA产生,从而缓解MPs和BPA联合作用对鲤鱼造成的氧化损伤,并且减缓鲤鱼体质量下降。研究表明,微塑料的存在会增加双酚A在鲤鱼肠道中的累积,且两者联合作用对鲤鱼产生了协同毒理效应,导致鲤鱼生长速率减缓,体质量下降。     

Bioactive Peptides from Algae: Traditional and Novel Generation Strategies,Structure-Function Relationships,and Bioinformatics as Predictive Tools for Bioactivity

Over the last decade, algae have been explored as alternative and sustainable protein sources for a balanced diet and more recently, as a potential source of algal-derived bioactive peptides with potential health benefits. This review will focus on the emerging processes for the generation and isolation of bioactive peptides or cryptides from algae, including: (1) pre-treatments of algae for the extraction of protein by physical and biochemical methods; and (2) methods for the generation of bioactive including enzymatic hydrolysis and other emerging methods. To date, the main biological properties of the peptides identified from algae, including anti-hypertensive, antioxidant and anti-proliferative/cytotoxic effects (for this review, anti-proliferative/cytotoxic will be referred to by the term anti-cancer), assayed in vitro and/or in vivo, will also be summarized emphasizing the structure–function relationship and mechanism of action of these peptides. Moreover, the use of in silico methods, such as quantitative structural activity relationships (QSAR) and molecular docking for the identification of specific peptides of bioactive interest from hydrolysates will be described in detail together with the main challenges and opportunities to exploit algae as a source of bioactive peptides.     

Metabolic Profiling and In Vitro Assessment of the Biological Activities of the Ethyl Acetate Extract of Penicillium chrysogenum “Endozoic of Cliona sp. Marine Sponge” from the Red Sea (Egypt)

Marine sponge-derived endozoic fungi have been gaining increasing importance as promising sources of numerous and unique bioactive compounds. This study investigates the phytochemical profile and biological activities of the ethyl acetate extract of Penicillium chrysogenum derived from Cliona sp. sponge. Thirty-six compounds were tentatively identified from P. chrysogenum ethyl acetate extract along with the kojic acid (KA) isolation. The UPLC-ESI-MS/MS positive ionization mode was used to analyze and identify the extract constituents while 1D and 2D NMR spectroscopy were used for kojic acid (KA) structure confirmation. The antimicrobial, antioxidant, and cytotoxic activities were assessed in vitro. Both the extract and kojic acid showed potent antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa with MIC 250 ± 0.82 µg/mL. Interestingly, the extract showed strong antifungal activity against Candida albicans and Cryptococcus neoformans with MIC 93.75 ± 0.55 and 19.53 ± 0.48 µg/mL, respectively. Furthermore, KA showed the same potency against Fusarium oxysporum and Cryptococcus neoformans with MIC 39.06 ± 0.85 and 39.06 ± 0.98 µg/mL, respectively. Ultimately, KA showed strong antioxidant activity with IC₅₀ 33.7 ± 0.8 µg/mL. Moreover, the extract and KA showed strong cytotoxic activity against colon carcinoma (with IC₅₀ 22.6 ± 0.8 and 23.4 ± 1.4 µg/mL, respectively) and human larynx carcinoma (with equal IC₅₀ 30.8 ± 1.3 and ± 2.1 µg/mL, respectively), respectively. The current study represents the first insights into the phytochemical profile and biological properties of P. chrysoenum ethyl acetate extract, which could be a promising source of valuable secondary metabolites with potent biological potentials.     

外源阿魏酸抑制鲜切苹果褐变机制研究

苹果在鲜切过程中易因遭受机械损伤而引发褐变,严重影响其感官品质、风味和商品价值。采用不同浓度外源阿魏酸溶液对鲜切‘红富士’苹果进行浸泡处理,以研究其抑制鲜切苹果褐变的机制。结果表明：1、5、8、10 g/L 的阿魏酸浸泡处理均能有效抑制鲜切苹果褐变,10 g/L 阿魏酸浸泡处理10 min 对鲜切苹果褐变的抑制效果最优;10 g/L 阿魏酸处理显著提高了鲜切苹果超氧化物歧化酶（SOD）活性及1,1-二苯基-2-三硝基苯肼（DPPH）自由基、2,2-联氨-双-3-乙基苯并噻唑啉-6-磺酸（ABTS）阳离子自由基的清除率,抑制了贮藏后期多酚氧化酶（PPO）活性,降低了表儿茶素等单一酚的含量,提高了对香豆酸的含量;添加5 mg/mL 表儿茶素会促进苹果浆液褐变,而添加5、10、20、40 mg/mL 对香豆酸均能抑制苹果浆液褐变。综上所述,外源阿魏酸处理可通过提高SOD 活性、抗氧化能力、内源褐变抑制物含量以及降低褐变底物含量来减轻鲜切苹果褐变。     

黄芪多糖的超声波-闪式协同提取工艺优化及抗氧化活性研究

以黄芪为原料,采用超声波-闪式协同提取黄芪多糖。以黄芪多糖得率为评价指标,采用单因素试验和正交试验,确定最佳提取工艺。结果表明,超声波提取最佳工艺条件为：料液比1∶30（g/mL）,超声温度70 ℃,超声时间40 min,超声波功率500 W,在此条件下,黄芪多糖得率为7.11%;在对超声波提取工艺优化的基础上,协同闪式提取,最佳闪式提取工艺参数为：提取次数3 次,闪提时间100 s,提取电压160 V,在此条件下,黄芪多糖得率为11.03%;体外抗氧化活性试验结果表明：当黄芪多糖质量浓度为1.0 mg/mL 时,其对1,1-二苯基-2-三硝基苯肼（1,1-diphenyl-2-picrylhydrazyl,DPPH）自由基和2,2-联氨-双-3-乙基苯并噻唑啉-6-磺酸（2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid),ABTS）阳离子自由基的清除率分别为66.27%和58.27%。本研究获得了黄芪多糖的最佳提取方法,得到的黄芪多糖具有较强的抗氧化作用。该方法可为黄芪多糖的提取及开发应用提供参考。     

宁波苦丁有效成分提取方法的比较及其抗氧化活性的研究

采用水蒸气蒸馏法(SDE)、乙醇法(EE)、超声波法(UWE)、微波法(MAE)和超临界CO2萃取法(SCDE)提取宁波苦丁有效成分,得率分别为:0.048%、0.011%、0.631%、0.522%和0.935%,毛细管GC-MS法分别鉴定出10、9、12、9和20种成分,体外抗氧化活性测试均显示了抗氧化结果,活性强度依次为:超临界CO2萃取法＞超声波法＞水蒸气蒸馏法＞乙醇法＞微波法.     

玉米小斑病抗性种质鉴定及生理生化分析

以200份玉米优良自交系为材料,2022-2023年夏分别进行小斑病菌的田间接种,综合两年数据共鉴定出高抗小斑病的玉米自交系3份,分别为K22、CML50和齐319;筛选到包括Mo17在内的抗性玉米自交系24份。选取K22和B73两个具有不同抗性水平的玉米自交系进行小斑病菌的室内接种。结果表明,48 h和72 h时,自交系K22叶片的病斑数、病斑面积和病斑面积比等各项指标均显著优于自交系B73,进一步验证田间鉴定的准确性。48 h或72 h时,高抗小斑病自交系K22与感病对照B73相比,5种防御酶活性增加14.32%～70.45%。