日本金龟子在中国适生区的预测

日本金龟子PopilliajaponicaNewman是一种重要的害虫 ,主要危害草坪和观赏植物。日本金龟子原产日本 ,现在已经分布于许多国家 ,并且造成了严重的经济损失。目前中国尚未有该虫分布。本文通过以计算机为基础的生态气候模型—CLIMEX ,利用气候数据来预测日本金龟子适合的地理分布区 ,预测结果是日本金龟子可以在中国大约 31个市、县地区生存 ,主要是沿海地区和长江流域 ,尤其是中国的中东部地区     

转 Bt基因抗虫棉对棉大卷叶螟抗性的研究

:转Bt基因抗虫棉对棉铃虫有很好的抗性,对棉大卷叶螟(SyleptaderogataFabricius)的抗性未见报道。作者研究表明,棉大卷叶螟在棉田为聚集分布型,低龄幼虫有集中为害习性;抗虫棉对其有很好的抗性,平均虫株率为2.2%,较常规棉中棉所12降低96.6%;百株虫量为133.8头,较常规棉降低88.4%。     

新疆野生果树及其分布格局

根据多年的野外调查和资料分析,首次较系统研究报道了新疆野生果树的种类、分布及现状,已知种类有102种(含变种、1亚种,不包括半野生果树),隶属10科,26属.新疆野生果树的种类分布北疆明显多于南疆.新疆野生果树的分布格局与地区的地理、气候等生态环境因子密切相关,呈现北疆多于南疆,西部比较丰富,山地多于平原的特点.从统计来看,分布在塔里木盆地的野生果树种类稍多于准噶尔盆地.就东西方向分布特点而论,无论是北疆还是南疆,野生果树多样性均表现为西部比较丰富,而东部比较贫乏,其原因主要是西部降水明显多于东部的.在新疆的几大山地中,天山山区的野生果树种类最为丰富,而昆仑山--阿尔金山和帕米尔高原最少,说明在干旱地区影响野生果树分布的生态因子中最重要的是水份条件.受降水条件的影响,新疆山地与平原野生果树物种多样性的差异十分明显,如塔里木盆地和准噶尔盆地中,包括若干重复出现的种在内,两大盆地仅有19种,而仅分布在天山山区的野生果树就有80种.     

猴头菌优良菌株筛选研究初报

通过对六个猴头菌菌株菌丝生长情况，子实体农艺性状和产量的比较试验发现，HN、RT和猴杰2号综合性状较优，适合新疆阿拉尔地区代料栽培。     

亚精胺对猕猴桃采后抗氧化酶活性的影响

 研究了不同亚精胺处理对猕猴桃采后抗氧化酶活性及保鲜效果的影响, 结果表明: 猕猴桃果实采后(8 ±2) ℃条件下贮藏12 d , SOD 活性达到高峰; POD、CAT、ASP 活性高峰相对SOD 推迟约13 d。不同亚精胺处理均不同程度地延缓了SOD 活性高峰的出现, 提高了SOD、CAT 的活性, 减少了MDA 的积累,降低了POD、ASP 的活性峰值, 延长了猕猴桃的贮藏保鲜期, 其中以Spd 与NAA 结合处理的效果最为显著。     

苹果梨中多酚氧化酶酶学特性的研究

 以苹果梨中的多酚氧化酶为研究对象, 对其酶的活性变化及其特性的研究表明, 苹果梨中的多酚氧化酶的最适pH 值是4. 6 , 最适温度是40 ℃; 亚硫酸氢钠、维生素C、柠檬酸对苹果梨中多酚氧化酶的抑制作用依次减弱, 硫酸钠几乎无抑制作用。不同底物和同底物不同浓度影响多酚氧化酶特性。     

滑菇优良品种筛选试验初报

本试验对 6个不同滑菇品种进行了菌丝体生长和制种观察 ;在栽培试验过程中进行了多点小试和中试 ,初选出Ph0 8号和Ph0 6号两个品种。Ph0 8的单盘产量比CK1高出 2 5 8% ,比CK2 高出 35 3% ;Ph0 6的单盘产量比CK1高出 2 1 5 % ,比CK2 高出 30 6 %。它们均属早生品种 ,适合辽宁地区的气候特点 ,在幼菇期菌盖呈半球形、桔红色、附着的粘液多 ,菌柄比对照短 ,菇体健壮 ,符合商品收购和产品加工的要求     

早熟、优质、耐贮梨新品种新梨7号选育研究

以库尔勒香梨为母本,早酥梨为父本,有性杂交选育成新梨７号品种。该品种同时兼备优质、早熟与耐贮藏性;该品种遗传了父本的早熟性,比父本更早熟１５~２０ｄ,盛花期~果实可食期约８０~９５ｄ,属于早熟品种;且遗传了母本品质性状的质地酥脆、耐贮、清香、阳面红晕,比母本果个大,果心小。果柄木质化,丰产抗风。新梨７号果实贮藏期的可溶性固形物、果实重量、果实硬度和果实前期腐烂率的变化与库尔勒香梨基本相似,但耐热能力高于母本。凡适宜香梨、早酥、苹果梨和巴梨种植的地区,都适宜该品种的种植。     

Metallothionein inhibits homocysteine-induced proliferation of rat vascular smooth muscle cells

AIM:To investigate the effect of metallothionein(MT) on proliferation of rat vascular smooth muscle cells (VSMCs) stimulated by homocysteine and its mechanism. METHODS:VSMCs proliferation was measured by [³-H]-TdR incorporation, mitogen-activated protein kinase(MAPK)activity were determined by immunoprecipitation method, the intracellular contents of MT and malondialdehyde (MDA)were assayed by -hemoglobin saturation method and TBA reaction, respectively, and lactate dehydrogenase (LDH) leakage was measured by NADH oxidation. RESULTS:Hcy(10^-6-10^-4 mmol/L) stimulated [³-H]-TdR incorporation by the VSMCs in a concentration-dependent manner. Compared with control, [³-H]-TdR incorporation in VSMCs treated with 0.1 mmol/L Hcy was increased by 4.2 fold (P＜0.01). Meanwhile, Hcy enhanced MAPK activity, MDA formation and LDH release (P＜0.01)in a concentration-dependent manner. Treatment of VSMCs with MT alone did not change above parameters, compared with control. However, MT (10^-6-10^-4 mol/L)attenuated significantly Hcy-stimulated proliferation of VSMCs (P＜0.01)in a concentration-dependent manner. And MT inhibited obviously Hcy-induced activation of MAPK activity, MDA formation and LDH release. Preincubation of VSMCs with 0.5 mmol/L ZnCl₂ for 6 h induced an increase cellular MT content by 5.7-fold (P＜0.01). The MT-overexpressed VSMCs resisted Hcy-stimulating action on MAPK activity, MDA formation and LDH leakage (P＜0.01). CONCLUSION:These results show that MT has an inhibitory effect on Hcy-induced VSMCs proliferation, and that MT could inhibit Hcy-stimulated MAPK activity and lipid peroxidation.     

Preparation of gfp-bcl-XL-contained recombinant adenovirus vector by the homologous recombination in bacteria

AIM: To prepare gfp-bcl-X_L-contained recombinant adenovirus(rAd-gfp-bcl-X_L).METHODS: Bcl-X_L gene was amplified from pEGFP-C₃-bcl-X_L, subcloned into shuttle plasmid and formed transfer plasmid of pAdTrack-CMV-bcl-X_L. Then pAdTrack-CMV-bcl-X_L was linealinzed with PmeI and co-transformed into BJ5183 bacteria with adenovirus genomic plasmid of pAdEasy-1. The identified recombinant adenovirus plasmid was digested with PacI and transfected into 293 cells to package recombinant adenovirus particles. The target gene was detected by PCR.RESULTS: There were about 35% positive recombinant bacterial clones after the co-transformation of pAdTrack-CMV-bcl-X_L and pAdEasy-1 into BJ5183. Recombinant adenovirus particle were produced and further amplified after the transfection of pAdEasy-1-gfp-bcl-X_L into 293 cells. PCR test indicated that the recombinant Ad contained bcl-X_L gene. The titer of the purified rAd-gfp-bcl-X_L was 6.5×10¹² PFU/L. CONCLUSIONS: The homologous recombination in bacteria is a convenient and high efficient method to prepare rAd-gfp-bcl-X_L. This affords a good gene transfer vector for the gene therapy in human’s diseases.