早熟、高产转基因抗虫常规棉品种——湘K25

概述了湘K25的选育经过，介绍了湘K25的特征特性、产量、纤维品质和抗病、抗虫等特点，并总结了其关键栽培技术。     

白屈菜CmFAD2基因的克隆及植物转化载体构建

通过对白屈菜低温应答过程的转录组分析发现膜脂不饱和化相关基因的表达在一定过程中发生变化,脂肪酸去饱和酶基因FAD2在随温度的变化趋势为正"V"型,且表达量变化显著。利用NCBI等在线软件对序列进行相关生物学信息分析,并对白屈菜FAD家族成员FAD2基因的完整开放阅读框(ORF)进行克隆,并命名为CmFAD2。选用克隆载体pMD-19-T,转化大肠杆菌DH5α,测序验证序列正确性及完整性。将目的基因与植物表达载体pRI-201-AN连接构建重组DNA pRI-201-AN-Cm FAD2,电击法转化农杆菌LBA4404,利用菌液PCR法验证成功。该基因可作为药用植物抗寒品种创制的候选基因。     

贵州省食用菌产业现状与可持续性发展分析

笔者分析了贵州省食用菌产业特点与产业优势,认为贵州食用菌产业在自然条件、交通条件以及政策条件等方面均具有较大优势;全省食用菌规模逐渐扩大,品牌效应凸显。进一步总结了贵州省食用菌产业存在的问题,即缺乏行业规范,产品结构较为单一,行业人才匮乏。继而提出了贵州省食用菌产业可持续性发展建议,即加大食用菌产业的开发程度,加强科技支撑及专业人才培养,政府统筹,建立行业标准,重视菌渣的综合开发利用,以实现本省食用菌产业的后发赶超和可持续性发展。     

株行距及穴苗数的配置对寒地水稻产量和品质的影响

为明确垦稻26和龙粳31高产优质栽培的株行距和穴苗数处理,采取裂区设计进行试验研究。结果表明,最优群体因品种而异,垦稻26在株距10cm、行距30cm、5苗/穴产量最佳,龙粳31则以株距13.3cm、行距27cm、9苗/穴产量最佳;垦稻26在5苗/穴、行株距30cm×10cm处理,有利于提高稻米的碾磨品质,不利于改善稻米的外观品质,营养品质较低,利于改善稻米的食味品质,且食味评分值高达86.5,显著高于最低处理;龙粳31在5苗/穴、行株距27cm×13.3cm处理,碾磨品质较高,不利于营养品质和外观品质的改善,食味品质得到明显改善,食味评分值高达86.0,与最低处理差异达显著水平。因此,高产优质栽培要因品种选择适宜的穴苗数和株行距,是实现水稻高产优质最为快捷、最为经济有效的措施。     

The M43 domain-containing metalloprotease RcMEP1 in Rhizoctonia cerealis is a pathogenicity factor during the fungus infection to wheat

Wheat(Triticum aestivum L.) is an important staple crop for global human. The necrotrophic fungus Rhizoctonia cerealis is the causal pathogen of sharp eyespot, a devastating disease of wheat. Herein, we identified RcMEP1, a zinc metalloproteaseencoding gene from R. cerealis genomic sequences, and characterized its pathogenesis function. RcMEP1 expressed at markedly-high levels during R. cerealis infection process to wheat. The predicted protein RcMEP1 comprises of 287 amino acid residues and contains a signal peptide and a M43 metalloprotease domain harboring the active site motif(HEVGHWLGLYH). The assays of Agrobacterium tumefaciens-mediated transient expression in Nicotiana benthamiana leaves indicated that RcMEP1 is an apoplastic elicitor of cell death, and that the predicted signal peptide functions and is required for secretion and cell death-induction. The purified RcMEP1 protein and its M43 domain peptide were individually able to induce plant cell death and H2 O2 accumulation, and to inhibit expression of host chitinases when infiltrated into wheat and N. benthamiana leaves, while the M43 domain-deleting peptide and negative control lacked the capacity. Moreover, compared with the control pretreatment, the purified RcMEP1 protein or its M43-domain peptide resulted in enhanced pathogenesis in the inoculated wheat, whereas the M43 domain-deleting peptide failed. These results suggest that RcMEP1 acted as an important pathogenicity factor during R. cerealis infection to wheat and that its signal peptide and M43 domain are required for the secretion and pathogenesis of RcMEP1. This study provides insights into pathogenesis role of M43 domain-containing metalloproteases during R. cerealis infection to wheat.     

优质、高产转基因抗虫棉杂交种苏杂668的选育与栽培技术

本文概述了苏杂668的选育过程，阐明了苏杂668的特征特性、产量水平、纤维品质和抗性表现，并提出其高产栽培技术措施。     

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.     

IWOS系统在配网故障处理中的应用

随着我国经济社会的不断发展,全社会用电量不断上升,对电网的可靠性、安全性和电能质量也提出越来越高的要求。由于历史原因,配网建设欠账较多,总体基础薄弱,发展落后于主网,区域、城乡之间发展不均衡,水平差异大,存在明显短板。随着电动汽车、分布式电源、微电网、储能装置的快速发展,对配电网的安全性、经济性、互动性、适应性提出越来越高的要求。在国家电网公司建设“大运行”体系、推进地调县调一体化进程背景下,建设安全智能的配网自动化系统成为当务之急,但现有配网线路大多存在着技术、设备落后等问题,自动化水平不高,难以直接建成大规模的配网自动化系统。     

心尖锚的力学分析

设计了一种六齿镍钛合金锚钩用于封堵器等二尖瓣、三尖瓣返流修复系统的心尖固定,并对其力学特性进行研究.通过分析心脏结构及解剖数据,确定锚钩形状和可控尺寸设计变量,利用Solidworks建立锚钩3D模型,运用Abaqus软件对23个不同尺寸锚钩模型的入鞘过程进行有限元计算,分析锚钩入鞘过程中的最大入鞘力、最大冯米塞斯应变和入鞘轨迹的影响因素.制作了一种规格锚钩实物,与计算结果进行对比分析.结果表明:鞘部长度、鞘部角度及齿宽对应力、应变的影响最大,可以通过减小鞘部长度、鞘部角度及齿宽,有效降低最大应力、应变值;厚度、曲率半径及齿宽对入鞘力起到决定性作用,而根长和角度对入鞘力的影响很小;轴向刺入深度主要通过控制鞘部长度及鞘部角度来定义,径向刺入深度则由曲率半径的大小所决定.研究可为需心尖固定的心脏介入产品设计提供一定的借鉴意义.     

基于电动汽车生态系统的中国电动汽车发展

电动汽车的推广依赖于整个电动汽车生态系统,只有整个健康的生态系统才能有效促进电动汽车的发展。电动汽车生态系统包括政府的推动、电动汽车用户的意愿、充电运营公司的运营方式、供电公司的运营方式和电动汽车动力电池的回收等,其中各个环节相互影响。从电动汽车的各个生态环节的目前研究现状及对电动汽车发展的影响进行研究,得出电动汽车发展需要注意的几个问题。