Monitoring the activation of neuronal nitric oxide synthase in brain tissue and cells with a potentiometric immunosensor

An all solid state potentiometric immunosensor (ASPI) has been developed to study the activation process of neuronal nitric oxide synthase (nNOS), the enzyme involved in the synthesis of nitric oxide generated under physiological conditions. At first, an all solid state H⁺-selective ISE was fabricated with the carboxylated poly(vinyl chloride) (PVC-COOH) film containing H⁺ ionophore, antibody was then immobilized on the polymer layer. The immunocomplex formation was detected by monitoring pH change due to interaction between urease labeled secondary antibody and antigen. Experimental parameters such as the amount of phosphorylated nNOS immobilized on the electrode surface and pH responses due to the antibody–antigen reaction were studied in detail. The calibration plot of the potentiometric potential vs. phosphorylated nNOS concentration exhibited a linear relationship in the range of 3.4–340.0 μg/ml. The calibration sensitivity of the phosphorylated nNOS immunosensor was −0.073 ± 0.002 mV/μg ml⁻¹. The detection limit of nNOS was determined to be 0.2 μg/ml based on five-time measurements (95% confidence level, k = 3, n = 5). The reliability of the immunosensor was examined with rat brain tissues as well as neuronal cells, and the results shown were good, implying a promising approach for a novel electrochemical immunosensor platform with potential applications to clinical diagnosis.     

A novel carbonyl reductase from Pichia stipitis for the production of ethyl (S)-4-chloro-3-hydroxybutanoate

An NADPH-dependent carbonyl reductase (PsCR) gene from Pichia stipitis was cloned. It contains an open reading frame of 849 bp encoding 283 amino acids whose sequence had less than 60% identity to known reductases that produce ethyl (S)-4-chloro-3-hydroxybutanoates (S-CHBE). When expressed in Escherichia coli, the recombinant PsCR exhibited an activity of 27 U/mg using ethyl 4-chloro-3-oxobutanoate (COBE) as a substrate. Reduction of COBE to (S)-CHBE by transformants in an aqueous mono-phase system for 18 h, gave a molar yield of 94% and an optical purity of the (S)-isomer of more than 99% enantiomeric excess.     

The crystal structure of BlmI as a model for nonribosomal peptide synthetase peptidyl carrier proteins

Carrier proteins (CPs) play a critical role in the biosynthesis of various natural products, especially in nonribosomal peptide synthetase (NRPS) and polyketide synthase (PKS) enzymology, where the CPs are referred to as peptidyl‐carrier proteins (PCPs) or acyl‐carrier proteins (ACPs), respectively. CPs can either be a domain in large multifunctional polypeptides or standalone proteins, termed Type I and Type II, respectively. There have been many biochemical studies of the Type I PKS and NRPS CPs, and of Type II ACPs. However, recently a number of Type II PCPs have been found and biochemically characterized. In order to understand the possible interaction surfaces for combinatorial biosynthetic efforts we crystallized the first characterized and representative Type II PCP member, BlmI, from the bleomycin biosynthetic pathway from Streptomyces verticillus ATCC 15003. The structure is similar to CPs in general but most closely resembles PCPs. Comparisons with previously determined PCP structures in complex with catalytic domains reveals a common interaction surface. This surface is highly variable in charge and shape, which likely confers specificity for interactions. Previous nuclear magnetic resonance (NMR) analysis of a prototypical Type I PCP excised from the multimodular context revealed three conformational states. Comparison of the states with the structure of BlmI and other PCPs reveals that only one of the NMR states is found in other studies, suggesting the other two states may not be relevant. The state represented by the BlmI crystal structure can therefore serve as a model for both Type I and Type II PCPs. Proteins 2014; 82:1210–1218. © 2013 Wiley Periodicals, Inc.     

Drosophila katanin-60 depolymerizes and severs at microtubule defects

Microtubule (MT) length and location is tightly controlled in cells. One novel family of MT-associated proteins that regulates MT dynamics is the MT-severing enzymes. In this work, we investigate how katanin (p60), believed to be the first discovered severing enzyme, binds and severs MTs via single molecule total internal reflection fluorescence microscopy. We find that severing activity depends on katanin concentration. We also find that katanin can remove tubulin dimers from the ends of MTs, appearing to depolymerize MTs. Strikingly, katanin localizes and severs at the interface of GMPCPP-tubulin and GDP-tubulin suggesting that it targets to protofilament-shift defects. Finally, we observe that binding duration, mobility, and oligomerization are ATP dependent.     

志留纪笔石Oktavitesexcentricus(Bjerreskov,1975)的古生物学特征及地层意义*

陕西紫阳地区在古地理上位于扬子台地西北缘,区域内志留纪地层发育,其中志留系兰多维列统(Llandovery)特列奇阶(Telychian)笔石相地层出露较为完整,笔石带较为连续。Oktavites excentricus(Bjerreskov,1975)是特列奇阶Oktavites spiralis笔石带重要的伴生分子,在世界范围内广泛分布。文中通过对紫阳地区一系列特列奇阶剖面研究后认为,Oktavites excentricus较短的化石延限和广泛的古地理分布使其具备地层对比潜力,这将为Oktavites spiralis笔石带的进一步细分提供依据。同时,Oktavites excentricus胞管为典型的奥氏笔石式,其笔石体的盘旋方式又与稍晚的Cyrtograptus lapworthi(Tullberg,1883)(笔石带化石,弓笔石类的早期代表)十分接近,因此,对该种的演化过程的研究也为讨论弓笔石的起源过程提供了更多参考。     

Lateral Organ Boundaries Domain 19 (LBD19) negative regulate callus formation in Arabidopsis

Plant Cell, Tissue and Organ Culture (PCTOC) - Callus is a remarkable regeneration tissue. The genes correlated with root development can be involved in regulating callus development in higher...     

黄猄蚁对橡胶盔蚧种群消长的影响

调查西双版纳地区黄猄蚁OecophyllasmaragdinaFabricius对橡胶盔蚧Parasaissetianigra(Nietner)种群数量和寄生蜂的影响。结果表明:黄猄蚁对橡胶盔蚧种群消长及寄生蜂均有影响。"有蚂蚁"枝条上介壳虫种群数量显著高于"无蚂蚁"枝条。"有蚂蚁"枝条介壳虫死亡率和寄生蜂都显著低于"无蚂蚁"枝条。说明黄猄蚁的存在影响了橡胶树介壳虫的种群繁殖率和死亡率。建议在今后综合防治中,充分利用蚂蚁与橡胶树介壳虫关系。通过驱逐橡胶树上的蚂蚁来有效遏制介壳虫的发生。