C-S-H中Al3+离子的固溶对表面吸附碱量的影响

研究了Al3+离子的固溶对C-S-H表面吸附Na+离子量的影响.实验结果表明,Al3+离子固溶于C-S-H结构中将使C-S-H表面所带的负电量增大,因而也就增大了C-S-H表面对Na+离子的吸附能力.     

The Three-component One-pot Synthesis of 4,6-Diarylpyrimidin-2(1h)-ones and 9-Phenyl-8-oxa-10,12-diaza-tricyclo[7.3.1.0~(2,7)]trideca-2(7),3,5-trien-11-one

1 Results Pyrimidinones (PMs) are a class of important heterocycles which have been well documented throughout the literature due to their biological importance. They exhibit a wide range of pharmaceutical and therapeutic properties[1].A rapid and efficient one-pot method for the synthesis of 4,6-diarylpyrimidin-2(1H)- ones and related heterocycles is described.The condensation of acetophenone derivatives,aldehydes and urea in the presence of sulfamic acid was employed to synthesize a variety of pyrimid...     

间套种植对根系土壤酶及养分复合系统的影响研究

通过池栽试验研究了玉米∥蚕豆、玉米∥鹰咀豆及3种单作作物生长盛期的根系空间分布特征,以及不同种植模式对土壤酶活性、养分含量空间分布的影响。结果表明,玉米∥蚕豆和玉米∥鹰咀豆地上生物量较对照均有不同程度的提高;0cm～30cm土层中玉米∥蚕豆根干重占总根重的比例较单作对照高10 78%,玉米∥鹰咀豆较对照低5 78%;根密度在垂直方向上可划分为4个类型区,0cm～20cm为高密度区、20cm～40cm为中密度区、40cm～60cm为低密度区、60cm以下为稀密度区;土壤酶活性可划分为4个层次:亚活跃层(0cm～10cm)、活跃层(10cm～30cm)、过渡层(30cm～40cm)和稳定层(40cm以下);根密度与土壤pH、有机质含量、全磷含量、全氮含量、有效磷含量呈显著或极显著相关。表3,参3。     

木材在机械加工中崩茬的控制

在木材的机械加工过程中，崩茬是比较容易出现的制造缺陷，如何有效的控制崩茬问题的出现是非常重要的。本文主要分析崩茬的原因以及平行四边形法则在控制崩茬问题上的应用。     

试论"代表先进社会生产力发展要求"是对历史唯物主义的新发展

中国共产党始终代表中国先进生产力的发展要求的论断,是站在历史唯物主义的角度,揭示出我们党兴旺发达的根本动力.     

近代中国科学技术落后的思考

中国曾经创造出遥遥领先于西方一千多年的灿烂的古代科学技术．但是，从１７、１８世纪以后，中国科学技术却开始滑坡，被此时取得高速发展的西方科学技术远远地抛到了后面．这一历史大换位，成为人们关注的问题．本文通过纵向和横向比较，综述了近代中国落后的史实，探析了落后的历史经济原因、政治原因和政策原因．警示今人记取史训，努力振兴中国现代科技     

Nuclear localization and signalling activity of phosphoinositidase C beta in Swiss 3T3 cells.

The hydrolysis of phosphatidylinositol 4,5-bisphosphate (PtdInsP2) is a widespread receptor-coupled signalling system at the plasma membrane of most eukaryotic cells. The existence of an entirely separate nuclear phosphoinositide signalling system is suggested from evidence that purified nuclei synthesize PtdInsP2 and phosphatidylinositol 4-phosphate (PtdInsP) in vitro and that a transient decrease in the mass of these lipids occurs when Swiss 3T3 cells are cultured in the presence of insulin-like growth factor-1 (IGF-1). These IGF-1-dependent changes in inositol lipids coincide with an increase in nuclear diacyglycerol and precede translocation to the nucleus and activation of protein kinase C (refs 5, 6). Circumstantial evidence that links these changes with mitosis comes from the isolation of a 3T3 clone that expresses the type-1 IGF receptor and binds IGF-1 peptide but does not respond mitogenically or show transient mass changes in nuclear inositol lipids. A key question is how IGF-1 initiates the rapid breakdown of PtdInsP and PtdInsP2 in the nucleus. Here we present evidence that nuclei of 3T3 cells contain the beta-isozyme of phosphoinositidase C, whereas the gamma-isozyme is confined to the cytoplasm and that IGF-1 treatment stimulates exclusively the activity of nuclear phosphoinositidase C.     

Prediction of the structure of a receptor-protein complex using a binary docking method.

To validate procedures of rational drug design, it is important to develop computational methods that predict binding sites between a protein and a ligand molecule. Many small molecules have been tested using such programs, but examination of protein-protein and peptide-protein interactions has been sparse. We were able to test such applications once the structures of both the maltose-binding protein (MBP) and the ligand-binding domain of the aspartate receptor, which binds MBP, became available. Here we predict the binding site of MBP to its receptor using a 'binary docking' technique in which two MBP octapeptide sequences containing mutations that eliminate maltose chemotaxis are independently docked to the receptor. The peptides in the docked solutions superimpose on their original positions in the structure of MBP and allow the formation of an MBP-receptor complex. The consistency of the computational and biological results supports this approach for predicting protein-protein and peptide-protein interactions.