iTRAQ-Based Proteomic Reveals Cell Cycle and Translation Regulation Involving in Peanut Buds Cold Stress

Russian Journal of Plant Physiology - Cold stress is one major threats to field crops. The cold tolerant ability is a key limiting factor for the popularization of peanut (Arachis hypogaea L.) in...     

A green and effective method for the determination of metalaxyl enantiomers in tobacco and soil by supercritical fluid chromatography–tandem mass spectrometry

We reported a new methodology for the stereoselective determination of metalaxyl enantiomers in tobacco and soil. The QuEChERS (quick, easy, cheap, effective, rugged, and safe) method was used for the extraction and clean-up of the tobacco and soil samples. Separation of the metalaxyl enantiomers was performed on an ACQUITY UPC2 Trefoil CEL1 chiral column coupled with supercritical fluid chromatography with tandem mass spectrometry (SFC-MS/MS), and the run time was only 5 minutes. Under the optimized conditions, the recoveries for the enantiomers were between 78.2% and 93.3% with intraday relative standard deviations (RSDs) ranging from 1.1% to 5.4%. The limit of detection (LOD) for the enantiomers in tobacco and soil varied from 0.005 to 0.007 mg/kg, and the limit of quantitation (LOQ) ranged from 0.017 to 0.020 mg/kg. In this method, only a small amount of methanol was consumed to obtain a rapid stereoselective separation. This proposed method showed good accuracy and precision and might be suitable for fast enantioselective determination of metalaxyl in food and environmental samples. The developed method was further validated by application to the analysis of authentic samples.     

Sl‐lncRNA15492 interacts with Sl‐miR482a and affects Solanum lycopersicum immunity against Phytophthora infestans

Long non‐coding RNAs (lncRNAs) are involved in the resistance of plants to infection by pathogens via interactions with microRNAs (miRNAs). Long non‐coding RNAs are cleaved by miRNAs to produce phased small interfering RNAs (phasiRNAs), which, as competing endogenous RNAs (ceRNAs), function as decoys for mature miRNAs, thus inhibiting their expression, and contain pre‐miRNA sequences to produce mature miRNAs. However, whether lncRNAs and miRNAs mediate other molecular mechanisms during plant resistance to pathogens is unknown. In this study, as a positive regulator, Sl‐lncRNA15492 from tomato (Solanum lycopersicum Zaofen No. 2) plants affected tomato resistance to Phytophthora infestans. Gain‐ and loss‐of‐function experiments and RNA ligase‐mediated 5′‐amplification of cDNA ends (RLM‐5′ RACE) also revealed that Sl‐miR482a was negatively involved in tomato resistance by targeting Sl‐NBS‐LRR genes and that silencing of Sl‐NBS‐LRR1 decreased tomato resistance. Sl‐lncRNA15492 inhibited the expression of mature Sl‐miR482a, whose precursor was located within the antisense sequence of Sl‐lncRNA15492. Further degradome analysis and additional RLM‐5′ RACE experiments verified that mature Sl‐miR482a could also cleave Sl‐lncRNA15492. These results provide a mechanism by which lncRNAs might inhibit precursor miRNA expression through antisense strands of lncRNAs, and demonstrate that Sl‐lncRNA15492 and Sl‐miR482a mutually inhibit the maintenance of Sl‐NBS‐LRR1 homeostasis during tomato resistance to P. infestans.     

三江平原七星河流域湿地植物多样性及影响因素

湿地植物多样性是生物多样性的重要组成部分,在维护湿地生态功能和湿地生态系统稳定性方面发挥着极其重要的作用。为研究七星河流域湿地植物的多样性,选择七星河流域的七星河国家级自然保护区和三环泡国家级自然保护区,分别于2016年和2017年,对该流域内湿地植物进行了实地植物样方调查,共计调查194个样方,利用TWINSPAN进行了样方群落划分,并采用广义线性模型分析了影响植物多样性的影响因素。结果表明七星河流域湿地植物共有532种,隶属于80科,212属,主要群落类型为湿苔草-隐果苔草群丛;狭叶甜茅群丛;萍蓬草-狐尾藻群丛;漂筏苔草群丛;小叶章-臌囊苔草群丛;甜茅-芦苇群丛;芦苇群丛;貉藻群丛等,狭叶甜茅群丛物种多样性较单一,芦苇群丛的物种多样性较丰富。广义线性模型分析结果得出物种多样性与植被密度密切相关,植被密度越大,物种的多样性越小。为七星河流域物种多样性研究提供了重要的基础数据。     

微花蛛毛苣苔在中国云南的发现及其补充描述

中越边境喀斯特地区是全球生物多样性热点地区,也是生物多样性保护的关键区域,近年来在该地区发现了多个蛛毛苣苔属植物的新种。微花蛛毛苣苔于2001年在越南北部喀斯特地区首次采集到标本,直到2018年才被发表出来,由于发表时仅基于一号花发育未成熟的标本,所以该物种的诸多形态特征仍不清楚。作者开展中越边境喀斯特地区植物多样性调查时,在我国云南东南部发现了微花蛛毛苣苔,并采集到花发育成熟的植株,对其进行了解剖观察和测量,现对该物种进行补充描述,并提供墨线图和野外生态照片以资辨认。微花蛛毛苣苔与腺花蛛毛苣苔在光滑无毛而反折的花萼以及被腺毛的花冠等形态上最相似,但不同之处在于微花蛛毛苣苔的叶上面幼时被褐色蛛丝状绵毛,后变近无毛,花序顶生,花冠长9～12 mm,蒴果直,不旋扭,长1.2～2.8 cm。微花蛛毛苣苔在滇东南的发现,说明中国南部喀斯特地区和越南北部喀斯特地区构成了一个完整的植物区系地理单元。     

限制性内切酶Mlu I蛋白及其硒代衍生物的制备

【背景】限制性内切酶Mlu I是一种常用的工具酶,在分子生物学领域发挥着重要的作用,其三维结构尚未被解析。【目的】在大肠杆菌中克隆表达、纯化重组Mlu I蛋白及其硒代蛋白,并进行结晶条件的研究。【方法】构建重组表达载体pET28b-Mlu I,在大肠杆菌BL21(DE3)pLysS中诱导表达,利用亲和层析和凝胶过滤层析纯化重组Mlu I蛋白和硒代Mlu I蛋白。对蛋白进行质谱检测、圆二色谱检测以及酶活检测,利用坐滴法进行结晶条件的筛选。【结果】构建了重组表达载体pET28b-Mlu I并纯化获得达到结晶纯度的蛋白,通过质谱检测确定硒代Mlu I蛋白中的8个甲硫氨酸全部被取代,结合酶活测试及圆二色谱检测确定了硒代对Mlu I蛋白的活性、结构无明显影响。采用坐滴法进行初步的晶体生长研究,重组蛋白目前已在1种条件下获得针状晶体并进行初步衍射,获得分辨率在0.32 nm左右的衍射数据。【结论】Mlu I蛋白及硒代Mlu I蛋白纯化体系的构建和结晶条件的研究,可为下一步解析Mlu I三维结构、作用机制的探讨及定向改造奠定基础。     

DNA水凝胶的制备及应用

脱氧核糖核酸(Deoxyribonucleic acid,DNA)不仅可作为生物遗传的物质基础,又以其可编程性、功能多样性、生物相容性和生物可降解性等优点,在生物材料的构建方面表现出巨大的潜力。DNA水凝胶是一种主要由DNA参与形成的三维网状聚合物材料,同时因其保留的DNA生物性能与自身骨架的机械性能的完美融合使得它成为近年来最受关注的新兴功能高分子材料之一。目前,基于各种功能核酸序列或通过结合不同的功能材料制备的单组分或多组分DNA水凝胶,已广泛用于生物医学、分子检测及环境保护的研究或应用领域中。文中主要总结了近十几年来DNA水凝胶制备方法上的研究进展,探讨了DNA水凝胶的分类策略,并进一步综述了DNA水凝胶在药物运输、生物传感、细胞培养等方面的应用研究。最后对DNA水凝胶未来的发展方向以及可能面临的挑战进行了展望。     

Ptk2b deletion improves mice folliculogenesis and fecundity via inhibiting follicle loss mediated by Erk pathway

Ptk2b has been found playing critical roles in oocyte maturation and subsequent fertilization in vitro. But what is the exact in vivo function in reproduction still elusive. Here, by constructing Ptk2b mutant mice, we found Ptk2b was not essential for mice fertility, unexpectedly, contrary to previously reported in vitro findings, we found Ptk2b ablation significantly improved female fecundity. Follicle counting indicated that the number of primordial follicles and growing follicles in matured mice was significantly increased in the absence of Ptk2b, whereas the primordial follicle formation showed no defects. We also found this regulation was in an autophosphorylation independent pathway, as autophosphorylation site mutant mice (PTK2B^Y402F) show no phenotype in female fertility. Further biochemistry studies revealed that Ptk2b ablation promotes folliculogenesis via Erk pathway mediate follicle survival. Together, we found a novel biological function of Ptk2b in folliculogenesis, which could be potentially used as a therapeutic target for corresponding infertility.