爱媛28’香橙砧与枳砧在南平市引种表现与评价

2017年引进早熟杂柑品种‘爱媛28’香橙砧和枳砧苗分别在大棚设施和露天进行试种,栽培4年调查比较两个砧木组合的生长表现、丰产性与果实品质,结果表明：‘爱媛28’香橙砧树表现生长势强,冠幅、树高、茎粗、结果枝、秋梢等生长量指标显著大于枳砧树,3a树初产1436 kg/667㎡,4a树2523kg/667㎡,显著高于枳砧4a树初产1809kg/667㎡;大棚种植香橙砧4a树果实10月下旬TSS11-12%,12月中旬TSS可达15%,与枳砧相当,可滴定酸比枳砧略高,两者固酸比均达18以上,口感风味极佳,两者单果重、果形指数、果皮厚度、可食率无显著性差异;未密封大棚4a树体经受2020年寒冬极端低温考验无明显冻害,抗旱抗寒能力中等,易感黑点病和流胶病,大棚种植能很好预防黑点病。综合评价爱媛28枳砧和香橙砧均适合在南平市种植,香橙砧比枳砧早期丰产性稳产性好,收益更高,香橙砧‘爱媛28’设施种植较枳砧更具优势。     

甘蓝型油菜MYB28转录因子对根肿菌和水杨酸的响应特征

MYB转录因子参与植物的生长发育和逆境胁迫过程,在植物防御相关信号反应中起着重要的调控作用。 为了明确MYB28在油菜与根肿菌互作中的作用,对感病甘蓝型油菜中双11中MYB28家族基因在根肿菌接种以及 水杨酸处理后的表达模式进行了分析。不同组织表达模式分析显示,相比于根和叶,BnaMYB28 在茎和种子中的表 达水平更高;BnaMYB28 基因在根肿菌和外源水杨酸处理下均有不同程度的表达响应,外源水杨酸处理下Bna⁃ MYB28-1 和BnaMYB28-3 上调表达,BnaMYB28-2 表达则受抑制。根肿菌侵染后,BnaMYB28-1 在整个侵染期表达 量均显著上调,但在加入水杨酸后表达被显著抑制;BnaMYB28-3 表达量在接菌后7 d和28 d显著上调,在关键皮层 侵染期（接菌后14 d）表达量与对照组相比没有变化,但在施加水杨酸处理后表达量显著上调。综上,外源水杨酸能 正向调控BnaMYB28-1 和BnaMYB28-3 表达,BnaMYB28-3 可能通过水杨酸信号路径参与油菜与根肿菌的互作。     

四种短体线虫的形态和分子生物学鉴定

 采用形态学和分子生物学方法对来自荷兰的藏橐吾和铃兰、泰国的高山榕、缅甸的香蕉等种苗(球)分别鉴定出玻利维亚短体线虫Pratylenchus bolivianus、铃兰短体线虫P. convallariae、咖啡短体线虫P. coffeae和斯佩奇短体线虫 P. speijeri。对这4种线虫的形态特征进行较为详细的描述后,认为头环、口针、侧区、生殖系统和尾形等形态特征是种类鉴定的重要依据;进一步利用引物28S-D2A/28S-D3Br扩增测序得到上述4种线虫的28S rRNA基因D2/D3区序列,序列分析发现玻利维亚短体线虫从欧洲到美洲的不同种群之间的遗传距离变异较小,仅为0~0.007;铃兰短体线虫同一种群不同个体之间的遗传变异较大,为0.006~0.029;咖啡短体线虫不同种群之间的平均遗传距离为0.013;斯佩奇短体线虫不同种群之间的平均遗传距离为0.010;咖啡短体线虫P. coffeae和斯佩奇短体线虫P. speijeri亲缘关系很近,二者种间平均遗传距离仅为0.026。本研究再次证明线虫28S rRNA基因D2/D3区基因序列可作为短体线虫种间鉴定的依据。     

车用28V高性能铁氧体永磁发电机的设计

对车用28V铁氧体永磁发电机进行了结构设计,确定出永磁体体积及发电机转子和定子的结构参数,设计了由基准电路、取样电路、触发电路等组成的三相半控桥式整流稳压电路,对设计的发电机及稳压电路进行了试验分析,验证了设计的合理性.     

Classification of Tomicus Species

Both morphological characters and a portion of of 28S rDNA sequences were used to identifying Tomicus species.The specimens were classed into groups with the following characters: 1) granules or punctures on interstria 2 on the declivity of the elytra;2) length of the elytral interstrial hairs and hairs arising from punctures;3) arrangement of pronotal punctures and hairs.These characters could be clearly examined under a binocular microscope at 30×magnification and they were applicable and valuable for the forest entomologists to identify Tomicus species.The phylogenetic tree established with difference in 28S rDNA sequence of D2 region revealed that the specimens of each group identified by morphological characters were also grouped together.The genetic distances of intra-species, inter-species and inter-genus were not overlapped. Genetic divergence of 28S rDNA was also useful for identifying Tomicus species.     

2013年粳稻4t实仓储藏一年后优势菌种的分离与鉴定

稻谷极易受到微生物的侵染,粮食微生物的活动不仅会影响到粮食的安全储藏,导致粮食腐坏变质,还会严重影响食用者的身体健康.采用GB 4789.15-2010对稻谷进行传统培养,并从中分离得到两株优势菌株.对分离出的优势菌株进行形态学观察,观察菌株在不同生长时期的形态及菌丝、孢子形态,初步判定两菌株均为曲霉.同时运用聚合酶链式反应对两菌株的ITS及28S片段进行扩增,扩增得517bp的ITS片度及560 bp的28S片段,将基因序列在Genbank中进行相似性比对,最终确定两菌株为溜曲霉(Aspergillus tamarii)和亮白曲霉(Aspergillus candidus).     

河北省长针线虫新纪录种松长针线虫Longidorus pinus Xu,Ye,Wang&Zhao的形态与分子鉴定

2018 年,在河北省保定市园林植物紫荆（Cercis chinensis）根围分离到一种长针线虫。经形态 学观察和 28S rDNA D2D3 区序列分析,将其鉴定为松长针线虫（Longidorus pinus Xu, Ye, Wang & Zhao）。 其雌虫主要形态特征为：雌虫体长 3 048~3 464 μm,唇区明显缢缩,宽 9.5~10.5 μm,侧器囊袋状,齿尖 针长 66.0~69.5 μm,导环距体前端 27.5~30.0 μm,尾长 31~33 μm,短圆锥形,尾长与肛门处体宽比值＝ 1.5~1.6。松长针线虫河北种群 28S rDNA D2D3 区与 GenBank 数据库的山西种群进行序列比对,相似性为 99.2%~99.9%。松长针线虫是河北省长针线虫新纪录种。紫荆是松长针线虫的新寄主。     

MicroRNA-145 inhibits epithelial-mesenchymal transition in human renal cancer A-498 cells by ADAM28

AIM: To investigate the inhibitory effect of microRNA-145 (miR-145) on epithelial-mesenchymal transition (EMT) in renal cancer A-498 cells. METHODS: The A-498 cells were transfected with miR-145 mimics (M145) and mimic negative control(MNC), which served as M145 group and MNC group, respectively. Mock control (MC) group was set up using untreated A-498 cells. The expression level of miR-145 in each group was detected by RT-qPCR. Transwell assay was used to detect the invasion ability of the cells. The protein expression of vimentin, E-cadherin and ADAM28 was determined by Western blot. Bioinformatic method was used to predict the target genes of miR-145. Antagonistic effect of ADAM28 over-expression on the inhibition of EMT by miR-145 was detected by Western blot. The relationship between miR-145 and ADAM28 was analyzed by dual-luciferase reporter assay. RESULTS: The expression level of miR-145 in M145 group was significantly up-regulated than that in MC group (P<0.05). The number of invasive cells in M145 group was 12.78±3.37, which was significantly lower than that in MC group (P<0.05). ADAM28 may be the target gene of miR-145. Compared with MC group, the protein expression of vimentin and ADAM28 in M145 group was significantly decreased (P<0.05), while the protein expression of E-cadherin was significantly increased (P<0.05).After ADAM28 over-expression, the protein expression of vimentin in the A-498 cells of M145 group was significantly increased (P<0.05), and the protein expression of E-cadherin was significantly decreased (P<0.05). The results of dual-lucife-irasei reporter assay showed that ADAM28 was a downstream target gene of miR-145. CONCLUSION: miR-145 may inhibit the expression of EMT-related proteins through the downstream target gene ADAM28 and inhibit the EMT process of renal cancer A-498 cells.     

罗氏沼虾白斑综合征病毒囊膜蛋白VP28基因的克隆及分析

根据已公布的罗氏沼虾白斑综合征病毒(WSSV)囊膜蛋白VP28基因序列设计一对特异性引物,从疑似患白斑病毒病的罗氏沼虾(Macrobrachium rosenbergii)中提取总DNA,并以此为模板,经PCR扩增、克隆并测序后将该片段通过GenBank比对,证实为WSSV的VP28基因;与20个已公布的WSSV VP28进行同源性比较,结果显示:从中国对虾、斑节对虾、南美白对虾、日本对虾、波纹龙虾提取的病毒株聚为一类,印度对虾WSSV VP28为另一类,罗氏沼虾WSSV VP28又单独为一类。根据测序结果推测VP28蛋白的二级结构在氨基酸的7～29区间可能为跨膜螺旋区,且该区域高度保守。