水稻根系育种研究进展

水稻（Oryza sativa L.）根系对水稻的生长发育及产量形成具有至关重要的作用。根据目前水稻根系育种的研究现状，分析了水稻根系育种对提高产量、改变形态特征和生理特性的重要性，并对其研究前景进行了分析和展望。     

人参皂苷Rb1对微血管自律性舒缩活动及大鼠心肌微血管内皮细胞内钙瞬时变化的影响

探讨人参皂苷Rb1(GSRb1)对人合谷穴区皮内微血管自律性舒缩活动振幅及大鼠心肌微血管内皮细胞(RMMECs)内游离钙离子瞬时变化的影响。利用激光多普勒血流测定仪结合离子导入仪检测微血管自律性舒缩活动的振幅。利用激光共聚焦显微镜、钙离子荧光探针Fluo-3AM检测ATP引起的RMMECs细胞内钙离子的变化及Rb1对其的影响。结果表明:试验确定了能够引起RMMECs细胞内游离钙离子释放的ATP的最低量为0.5μg·mL-1,瞬时升高差异显著的剂量是0.7μg·mL-1,能够影响RMMECs细胞内钙离子变化的GSRb1的最低量为8μg·mL-1。RMMECs经8μg·mL-1 GSRb1孵育后,能够刺激细胞内游离钙离子释放的ATP的最低量升高为1.5μg·mL-1。本研究说明,提高微血管自律运动振幅的中药成分GSRb1能够通过对RMMECs胞内钙离子的影响,提高RMMECs对ATP的耐受能力(ATP的刺激量由0.5μg·mL-1升高到1.5μg·mL-1)。     

试验统计方法课程教学改革探索与实践

介绍了试验统计方法课程的基本理论体系和教学目标,指出了试验统计方法课程教学中存在的主要问题,并提出了课程教学改革理念及思路,以为试验统计方法课程教学改革提供参考。     

110kV数字化变电站扩建主变的关键技术问题

文章针对某主变扩建项目在施工调试工程中遇到的110 kV过程层A/B网交换机VLAN划分问题,部分GOOSE链路、SV链路怎么完善等关键技术问题进行分析,并给出了合理的解决方案,保证了某变电站扩建3号主变压器的顺利投运,解决了该站即将面临的主变过载问题;提高了该站的运行可靠性及供电可靠性。     

快速灵敏的甘蔗线条花叶病毒免疫学检测体系的建立

 甘蔗花叶病广泛存在于我国甘蔗种植区,严重影响甘蔗产业的高质量发展。近年来甘蔗线条花叶病毒在蔗区肆虐,尽管针对其的血清学检测技术已经建立,但是快速、准确、高通量的检测方法亟待发掘。本研究制备了^SCSMVCP的抗血清,特异性高,与引起甘蔗花叶病的另两种病原 (高粱花叶病毒和甘蔗花叶病毒) 间没有血清学交叉反应。基于该多克隆抗体,建立了直接抗原包被的ELISA、斑点杂交、Western blot和基于多抗的免疫试纸条检测技术。开发的免疫试纸条检测技术能快速、准确、高通量应用于田间病毒鉴定。本文提供了基于血清学的快速、准确、高通量,且便捷的甘蔗线条花叶病毒检测技术,有助于我国蔗区甘蔗花叶病的监测与防控。     

Protective effect of curcumin analogue L6H4 on diaphragm of type 2 diabetic rats

AIM: To investigate the protective effect of curcumin analogue L6H4 on diaphragm of type 2 diabetic rats.METHODS: SPF male Sprague-Dawley rats (n=40) were randomly divided into 5 groups: normal control (NC) group, high fat (HF) group, high fat+L6H4 treatment (FT) group, diabetes mellitus (DM) group and DM+L6H4 treatment (DT) group. The rats in the later 4 groups were fed with high-fat diet. After 4 weeks of high-fat diet fee-ding, the rats in DM and DT groups were intraperitoneally injected with streptozotocin to induce type 2 diabetes melliutus. The rats in FT and DT groups were given L6H4 by gavage for 8 weeks. Blood glucose and blood lipid levels were detected biochemically. Fasting serum insulin (FINS) level was measured by radioimmunoassay and insulin resistance index (HOMA-IR) was calculated. Serum adiponectin (APN) level was measured by ELISA. The morphological changes of the diaphragm were observed under light and transmission electron microscopes. Lipid deposition and the activity of succinate dehydrogenase (SDH) and NADH-tetrazolium reductase (NADH-TR) were observed by enzyme histochemical staining. The content of malondialdehyde (MDA) and the activity of superoxide dismutase (SOD) in the diaphragm were measured by thiobarbituric acid method and hydroxylamine method, respectively. The protein expression of adiponectin receptor 1 (AdipoR1) in the diaphragm was determined by immunohistochemistry and Western blot. RESULTS: The levels of blood lipids, blood glucose, FINS and HOMA-IR in HF and DM groups were higher than those in NC group, but decreased after L6H4 treatment. The serum APN level in HF and DM groups was lower than that in NC group, but increased after treatment with L6H4. The muscle fibers of the diaphragm were shrunk, fat particles accumulated in the muscle fibers, and the mitochondria were slightly swollen in HF and DM groups. The diaphragmatic fibrosis was obvious in DM group. These lesions were relieved after L6H4 treatment. Compared with NC group, the level of MDA and the activity of SDH and NADH-TR in the diaphragm were increased in HF and DM groups, but decreased after treatment with L6H4. The activity of SOD and the expression of AdipoR1 in the diaphragm were lower than those in NC group, but increased after L6H4 treatment.CONCLUSION: The curcumin analogue L6H4 exerts a protective effect on diaphragm in type 2 diabetic rats. The strengthened protein expression of AdipoR1, the increased serum level of APN, and anti-lipid peroxidation may be involved in the process.     

云南省食用菌产业技术标准体系建设研究

分析了食用菌标准化现状，归纳目前食用菌标准体系存在的主要问题，提出云南省食用菌标准体系建设的原则与依据，按照产前、产中、产后划分标准类别，构建云南省食用菌产业技术标准体系。     

奶牛TNMD基因的克隆与原核表达

从奶牛组织中克隆Tenomodulin(TNMD)基因的cDNA序列,采用双酶切后连接表达载体pGEX-4T-1,转入大肠杆菌BL21中进行诱导表达。结果表明,TNMD基因的序列全长为957 bp,通过双酶切构建的表达载体pGEX-TNMD在BL21大肠杆菌中成功表达了分子量为59.68 kDa的融合蛋白。