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天然芸苔素属于甾体类植物内源生物活性物质,其骨架为甾醇,其中芸苔素内酯生物活性最强,被称为第六类植物激素,是高效、广谱、无毒的植物生长调节剂(PGR)。为更好地将芸苔素推广应用于农业生产,本文概括了芸苔素内酯的生物活性及在粮食、果蔬等作物上的应用。探讨了芸苔素内酯在提高种子活力,促进作物生长,大幅度促进产量提升以及品质改善,提升作物抗逆性,缓解农药对作物影响的研究概况及取得的进展,指出了芸苔素内酯的应用是作物增产增收的关键途径,同时,能够减少化肥、农药的施用量,减少作物种植成本与减轻环境污染,将带来显著的经济效益。 相似文献
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Antimicrobial peptides are a class of proteins with antibacterial functions. In this study, the anti-lipopolysaccharide factor isoform 3 gene (ALFPm3), encoding an antimicrobial peptide from Penaeus monodon with a super activity was expressed in Chlamydomonas reinhardtii, which would develop a microalga strain that can be used for the antimicrobial peptide production. To construct the expression cluster, namely pH2A-Pm3, the codon optimized ALFPm3 gene was fused with the ble reporter by 2A peptide and inserted into pH124 vector. The glass-bead method was performed to transform pH2A-Pm3 into C. reinhardtii CC-849. In addition to 8 μg/mL zeocin resistance selection, the C. reinhardtii transformants were further confirmed by genomic PCR and RT-PCR. Western blot analysis showed that the C. reinhardtii-derived ALFPm3 (cALFPm3) was successfully expressed in C. reinhardtii transformants and accounted for 0.35% of the total soluble protein (TSP). Furthermore, the results of antibacterial assay revealed that the cALFPm3 could significantly inhibit the growth of a variety of bacteria, including both Gram-negative bacteria and Gram-positive bacteria at a concentration of 0.77 μM. Especially, the inhibition could last longer than 24 h, which performed better than ampicillin. Hence, this study successfully developed a transgenic C. reinhardtii strain, which can produce the active ALFPm3 driven from P. monodon, providing a potential strategy to use C. reinhardtii as the cell factory to produce antimicrobial peptides. 相似文献
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黑胚病是小麦生产的重要籽粒病害,麦根腐平脐蠕孢(Bipolaris sorokiniana)是黑胚病的主要致病菌。为分析小麦抗黑胚病遗传规律并检测抗性位点,本研究以抗黑胚病小麦品系山农4143与感病品系宛原白1号的F7代重组自交系(RIL)群体为材料,于2018~2019年在3个试验点种植,采用“孢子液喷洒、套袋保湿”的方法进行接菌鉴定,用“主基因+多基因混合遗传模型”进行遗传分析,并挑选极端抗、感自交系构建混池、结合小麦660K SNP芯片进行混合分组分析(BSA)。研究结果显示小麦品系山农4143对黑胚病抗性符合“4对主基因加性-上位性遗传模型”,主基因遗传力为0.88~0.95;通过BSA检测到黑胚病抗性位点36个,分别位于1A、2B(6)、2D(2)、3A、3B(2)、3D、4A(6)、4D、5A(4)、5B(6)、5D(3)、7A、7B和7D共14条染色体上,A、B、D染色组上分别为13、 15和8个,36个位点中有18个为抗黑胚病新鉴定位点。本研究结果为小麦抗黑胚病位点的精细定位和抗性育种中分子标记的开发奠定了基础。 相似文献
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Usman Ijaz Michael Ayliffe Kedar Adhikari Harbans Bariana Urmil Bansal 《Plant pathology》2020,69(7):1227-1236
Uromyces viciae-fabae, rust of faba bean, parasitizes other legume crops such as lentils (Lens culinaris) and field peas (Pisum sativum) in some environments. In this study we examined the host range of two Australian isolates of U. viciae-fabae collected and purified from a faba bean crop and classified as U. viciae-fabae ex V. faba. Field pea (P. sativum), chickpea (Cicer arientinum), lupin (Lupinus spp.), lentil (L. culinaris), and mung bean (Vigna radiata) genotypes were tested with these isolates, as well as resistant and susceptible genotypes of the faba bean host. Race specificity for these two pathogen isolates was observed on Vicia faba, with two faba bean genotypes showing partial resistance. Both U. viciae-fabae isolates also colonized field pea seedlings and successfully produced uredinia under glasshouse conditions, despite this fungus not being known as a pathogen of Australian field pea crops. No sporulation of either isolate of U. viciae-fabae ex V. faba was observed on any of the remaining legume species tested. However, obvious differences in fungal growth were observed, ranging from small infection sites with very rare haustorium formation in mung bean to more extensive growth and the development of potential uredinial structures in chickpea. These observations are discussed in relation to the phylogenetic relationship of these host and nonhost species. 相似文献
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A. Susan M. K. Yadav S. Kar S. Aravindan U. Ngangkham S. Raghu S. R. Prabhukarthikeyan U. Keerthana S. C. Mukherjee J. L. Salam T. Adak A. Banerjee P. C. Rath 《Plant pathology》2019,68(3):537-546
Rice blast disease caused by the fungus Magnaporthe oryzae is one of the most devastating diseases causing huge losses worldwide. In the present study, major blast resistance genes were investigated in landraces originating from northeastern India. Based on phenotypic evaluation, 288 landraces were classified into three distinct groups: resistant (75), moderately resistant (127) and susceptible (86). The genetic frequencies of the 18 major blast resistance genes were between 6.2% and 27.4%, with only two genotypes possessing a maximum of nine blast resistance genes. The cluster and population structure analysis grouped the landraces into two groups. Through principal coordinate analysis, the scatter plots partitioned the resistant and moderately resistant landraces into different groups. Analysis of molecular variance showed maximum (96%) diversity within populations and least (4%) diversity between populations. Association analysis identified six markers, CRG4_2, RM72, tk59-2, pi21_79-3, RM1233 and RM6648, that are significantly associated with blast disease and explained a phenotypic variance of 1.1–6.5%. The associated genes could be used in marker-assisted rice breeding programmes for gene pyramiding to develop rice varietal resistance against blast disease. The present study represents a valuable blast resistance genetic resource that could be used for identification of new R genes, donors for blast resistance, and genomic studies. 相似文献
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我国云南、湖北和山东葡萄产区霜霉病菌对甲霜灵的抗性检测 总被引:1,自引:0,他引:1
为明确我国云南省宾川县、湖北省公安县和山东省烟台市葡萄产区霜霉病菌对甲霜灵的抗性发生态势,采用叶盘漂浮法测定了这3个产区共127株葡萄霜霉病菌对甲霜灵的抗性频率及抗性水平。结果显示,不同区域间病菌的抗性频率和抗性水平均存在差异。其中,湖北省公安县霜霉病菌的抗性频率和抗性水平均较高,抗性频率达92.0%,高抗菌株占76.0%,低抗菌株占16.0%,敏感菌株占8.0%;山东省烟台市霜霉病菌的抗性频率为74.0%,低抗菌株占64.0%,高抗菌株占10.0%,敏感菌株占26.0%;云南省宾川县霜霉病菌的抗性频率和抗性水平均较低,抗性频率为29.6%,敏感菌株占70.4%,低抗菌株占29.6%,无高抗菌株。 相似文献
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Peritrophic matrix/membrane (PM) critically prevents the midgut of insects from external invasion by microbes. The proteins in the peritrophic membrane are its major structural components. Additionally, they determine the formation and function of this membrane. However, the role of PM proteins in immune regulation is unclear. Herein, we isolated a novel PM protein (MdPM-17) from Musca domestica larvae. Further, the function of MdPM-17 in regulating host innate immunity was identified. Results showed that the cDNA of MdPM-17 full is 635 bp in length. Moreover, it consists of a 477-bp open reading frame encoding 158 amino acid residues. These amino acid residues are composed of two Chitin-binding type-2 domain (ChtBD2) and 19 amino acids as a signal peptide. Moreover, tissue distribution analysis indicates that MdPM-17 was enriched expressed in midgut, and moderate levels in the fat body, foregut, and malpighian tubule. Notably, MdPM-17 recombinant protein showed high chitin-binding capacity, thus belongs to the Class III PM protein group. MdPM-17 protein silencing via RNA interference resulted in the expression of antimicrobial peptide (defensin, cecropins, and diptericin) genes, and this occurred after oral inoculation with exogenous microbes Escherichia coli (Enterobacteriales:Enterobacteriaceae), Staphylococcus aureus (Bacillales:Staphylococcaceae), and Candida albicans (Endomycetales:Saccharomycetaceae)). Therefore, all the antimicrobial peptide (AMP) gene expression levels are high in MdPM-17-depleted larvae during microbial infection compared to controls. Consequently, these findings indicate that MdPM-17 protein is associated with the antibacterial response from the housefly. 相似文献