用呋喃丹防治蝼蛄试验

通过采用呋喃丹每床 (2 0m2 )施用 0、10 0、2 0 0、4 0 0g防治蝼蛄的试验 ,第一天防治效果达 79.7% ,第三天平均蝼蛄死亡 2 .3头·m-2 ,第四天很少发现死亡虫尸。试验表明 :每床施用 10 0g即可达到较好的防治效果 ;呋喃丹防治地下害虫对苗木不产生药害。     

Further observations of almond stem pitting 1

Two disorders of almond, know as 'stem pitting’and‘graft union necrosis (black line)', were described years ago from Puglia (southern Italy). The etiology of these diseases was uncertain, the causal agent unknown and reliable diagnostic methods were not available. Investigations were therefore carried out to identify Prunus species and/or cultivars as possible indicators for a quick and reliable diagnosis. In 1990, two different almond sources (cv. Filippo Ceo) affected by black line and stem pitting were budded onto seedlings of P. persica, P. cerasifera, P. amygdalus cv. Don Carlo, GF305, self-rooted cuttings of GF677 (P. persica×P. amygdalus) and onto Don Carlo and GF305 seedlings that had been already grafted with almond cvs Genco, Tuono and Filippo Ceo. At least two inoculated plants were inspected each year for the presence of symptoms on the woody cylinder after removal of the cortex. Stem pitting developed on P. persica and P. cerasifera seedlings during the first year after graft inoculation. On the grafted plants that had been inoculated, pitting and grooving of the wood were much more pronounced in cvs Filippo Ceo and Genco, with a higher incidence when GF305 was used as rootstock. Clear symptoms were observed (from the first year in cvs Tuono and Genco), regardless of the rootstock, all along the junction line and often not associated with pitting of the rootstock and scion.     

青藏高原东北部酸模属植物种子萌发特性的研究

研究了青藏高原东北部高寒地区蓼科酸模属(Rumex)5种植物种子特征，结果表明发芽温度范围、发芽适温、发芽所需的天数以及发芽率对种子萌发特性有不同的影响。     

Effect of EGFP gene transfection on the cell cycle distribution of primary cultured human chondrocytes

AIM: To investigate the effect of enhanced green fluorescence protein (EGFP) gene transfection on the cell cycle distribution of primary cultured human chondrocytes in order to establish a tracking method of cultured human nasoseptal chondrocytes. METHODS: pEGFP-N1 plasmid was amplified in E.coli, and purified by high purity kit. Primary cultured human chondrocytes,which were initially obtained from the nasoseptal cartilage, were cultured in vitro and transferred with pEGFP-N1 by means of electroporation with Amaxa nucleofector device. Transfering process and transient expression were evaluated by laser scanning confocal microscope (LSCM), the transfer efficiency and the cell cycle distribution were evaluated by flow cytometry. RESULTS: There was significant expression of EGFP at 24 h after transferring. The transfection efficiency of pEGFP-N1 into primary cultured human chondrocytes reached 35.37％ at 48 h. It didn't affect the process of cell adherance and had no effect on the cell cycle distribution. CONCLUSION: Primary cultured human chondrocytes, which were transfected with pEGFP, are alive in vitro, and the transferring process doesn't affect the cell cycle distribution. These results suggest that pEGFP-N1 is an ideal transient expression vector for primary cultured human chondrocytes and it might be a well tracer in construction tissue engineered cartilage.     

Roles of the Kv1.2, Kv1.5, Kv2.1 potassium channels in hypoxia pulmonary vasoconstriction

AIM: To determine the role of Kv1.2, Kv1.5, Kv2.1 in the hypoxia pulmonary vasoconstriction (HPV). METHODS: Male Wistar rats were divided into two groups: normoxic group and hypoxic group. The single smooth muscle cell was obtained from pulmonary artery of Wistar rats with acute enzymatic digestion method. The conventional whole-cell patch clamp technique was used to record the resting membrane potential (Em) and the potassium currents of voltage-gated potassium channel (IKv) in rat pulmonary arterial smooth muscle cells (PASMC). Intracellular application of Kv1.2/Kv1.5/Kv2.1 antibodies (1∶125) was conducted through the whole-cell patch clamp system. RESULTS: ① Em of PASMC was depolarized after 24 h hypoxia compared with that of control cells . IKv of PASMC was decreased after 24 h hypoxia, . ② The mixture of Kv1.2/Kv1.5/Kv2.1 antibodies depolarized Em and inhibited IKv in PASMC from normoxic rat, whereas the mixture of Kir2.1/Kir2.3/Kir4.1 antibodies had no effects on them. ③ The mixture of Kv1.2/Kv1.5/Kv2.1 antibodies and the mixture of Kir2.1/Kir2.3/Kir4.1 antibodies had no effects on IKv and Em from rats hypoxic for 24 h. CONCLUSION: Kv1.2, Kv1.5, Kv2.1 might be oxygen sensitive potassium channels which mediated HPV.     

Gene expression of 5α-reductase (type 2) in reproductive gland of pubertal diabetic rats

AIM: To study the molecular mechanism of reproduction dysfunction in pubertal diabetic rat, the level of 5α-reductase (type 2) mRNA in testis, epididymis and prostate in diabetic rat was detected. METHODS: The gene expression of 5α-reductase (type 2) was detected by Northern blot. RESULTS: In the caput of the epididymis, the expression of 5α-reductase (type 2) mRNA of D and ID groups was less than that of C group. CONCLUSION: The decreased expression of 5α-reductase (type 2) results in the decreased production of dihydrotestosterone, which influences the development and function of reproduction system in pubertal rats.     

不同刈割强度下羊草转录组研究

刈割是一种重要的草地管理措施,刈割留茬高度直接影响草地生产力及群落结构,在牧草生产中具有重要意义。为研究羊草在不同刈割强度下的转录响应,利用Illumina HiSeq-PE150高通量测序技术,对不同刈割留茬高度(0,2,4,8,12 cm)处理下羊草再生叶片进行了转录组测序。共得到139767803条读长(reads),41.94 Gb原始数据。经过过滤、质控与从头组装后,总共得到转录本270207条,总长度为191.6 Mb。通过与多种数据库比对得到48097条单基因簇(Unigene)注释结果。筛选出了所有刈割强度处理与不刈割对照组显著差异基因共2579条,经过生物信息分析,将其定位到碳水化合物代谢、损伤应答、过氧化氢分解、植物激素信号转导等功能与代谢通路。利用聚类方法得到了随着刈割强度增强,表达量规律变化的基因,分别富集到了过氧化物酶体、光合作用等代谢途径。对羊草在不同刈割高度下的转录组进行了研究,为草本植物分子生物学研究提供了宝贵的数据资源,对于解析羊草响应刈割的分子调控机制及相关基因挖掘具有重要指导意义。     

旱、盐胁迫下黄芪种子萌发及其对水杨酸的响应

通过测定不同浓度聚乙二醇(PEG)和NaCl胁迫下膜荚黄芪(Astragalus membranaceus)和蒙古黄芪(A.membranaceus var.mongholicus)种子的最终发芽率、发芽势、简化活力指数、苗长、根长、苗干重、根干重等指标,以及不同施用方式和浓度的水杨酸(SA)对重度PEG和NaCl胁迫下两种黄芪种子最终发芽率的影响,旨在研究两种黄芪种子对PEG和NaCl胁迫响应方式的异同及SA对两种黄芪种子在重度PEG和NaCl胁迫下保护效果的差异。结果表明,低浓度PEG和NaCl只能促进膜荚黄芪种子萌发。在-0.5 MPa PEG和-0.7 MPa NaCl处理下,蒙古黄芪种子的活力指数显著优于膜荚黄芪种子(P0.05)。SA浸种能促进重度PEG和NaCl胁迫下两种黄芪种子的最终发芽率。蒙古黄芪种子的耐胁迫性高于膜荚黄芪种子。两种黄芪种子对SA的响应方式有区别。SA浸种处理优于拌种处理。     

棘孢木霉葡聚糖酶基因Glu1的克隆及原核表达

从棘孢木霉(Trichoderma asperellum)ACCC30536中克隆获得一个葡聚糖酶基因Glu1,其cDNA全长984bp,编码327个氨基酸。该葡聚糖酶属于Glyco-hydro-12家族,推测为β-1,4-葡聚糖酶,与深绿木霉IMI 206040的Glycohydro-12家族蛋白(XP_013940397.1)有91%相似性,且亲缘关系较近。运用qRT-PCR技术检测9种诱导条件下棘孢木霉Glu1基因的表达水平,结果表明,Glu1基因能参与棘孢木霉对山新杨(Populus davidiana×P.alba var.pyramidlis)或杨树病原菌的识别。构建原核表达载体并获得重组蛋白rGlu1。酶活特性分析结果表明,该酶最适pH为4.5,最适温度为45℃,且酶活性随诱导时间延长逐渐升高,在5h达到稳定。