生物工程专业实验教学体系的改革与实践

为提高生物工程专业实验教学质量,促进学生专业知识体系的构建和实践技能的提升,本文以湖南中医药大学生物工程专业实验教学改革为例,从课程体系、教学内容、实验项目、教学条件、教学方法、考核方式等六个方面讨论了基于课程体系整合和实验项目设计的专业实验教学体系改革。通过实验课程体系的调整优化,学生的学习积极性显著提高,综合素质和水平也明显上升,取得了良好的教学效果。     

反硝化墙去除地下水硝酸盐研究进展

地下水硝酸盐污染越来越来越严重,过量摄入硝酸盐严重危害人类和家畜健康。反硝化墙是一种建造简单、无需管理维护的地下水硝酸盐原位修复技术。本文总结了反硝化墙对地下水中硝酸盐的去除效果、填充碳源种类、使用寿命及不利影响。     

The effect of hexamethylene diisocyanate modified ALCELL lignin as a coupling agent on the flexural properties of oil palm empty fruit bunch – polypropylene composites

ALCELL lignin has been employed as a coupling agent in oil palm empty fruit bunch (EFB)–polypropylene (PP) composites. The lignin has been chemically modified with hexamethylene diisocyanate (HMDI). Evidence for the reaction between HMDI and lignin has been observed by using Fourier transform infrared (FTIR) analysis. The effect of lignin as a coupling agent on the flexural properties has been studied. The results show that the HMDI‐modified lignin is able to impart greater compatibility between EFB and PP. This is reflected in the greater flexural strength shown by the composites with HMDI‐modified lignin than those with the unmodified lignin. Scanning electron microscopy studies show that HMDI‐modification of lignin results in a better blending and compatibility between lignin and PP matrix. The glass transition temperature of lignin increases as the level of HMDI modification is increased. © 2001 Society of Chemical Industry     

Synthesis and characterization of secondary doped polypyrrole/organic modified attapulgite conductive composites

Secondary doping method was introduced into fabricating polypyrrole/oganic modified attapulgite conductive composites. The preparation conditions, such as amount of hexadecylpyridinium chloride (CPC, modifying agent), organic modified attapulgite (OATP), and HCl (secondary dopant) have been optimized to get the composites with the highest conductivity. When m_CPC/m_ATP, m_OATP/m_Py, and n_HCl/n_SA (SA is sulfamic acid) reaches 0.03, 0.6, and 0.5, respectively, the PPy/OATP composites possess the highest conductivity of 87.59 S cm^?1 as well as the highest thermal degradation temperature of 249.29°C. Scanning electron microscopy, transmission electron microscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, UV‐Visible diffuse reflectance study, and X‐ray photoelectron Spectroscopy results showed that PPy chains form the core‐shell structure and may combine with OATP via π–π stacking interaction. Thermogravimetric analysis showed that the thermal stability of PPy/OATP‐SH composites was enhanced and these could be attributed to the retardation effect of OATP as barriers for the degradation of PPy. This method may open a new door for PPy‐based composites with special structures, higher performance, and thus broader application ranges. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41407.     

降低干熄焦焦炭烧损率的研究

分析了干熄焦焦炭烧损率的原因。通过控制影响烧损率的因素,使焦炭烧损率由1.2%下降到0.9%。按照生产焦炭100万t/a计算,每年可减少烧损1 000t,创经济效益100余万元,并延长了干熄炉的使用寿命和年修间隔时间。     

Anti-TMV Activity of Malformin A1, a Cyclic Penta-Peptide Produced by an Endophytic Fungus Aspergillus tubingensis FJBJ11

Plant-associated microorganisms are known to produce a variety of metabolites with novel structures and interesting biological activities. An endophytic fungus FJBJ11, isolated from the plant tissue of Brucea javanica (L.) Merr. (Simaroubaceae), was proven to be significantly effective in producing metabolites with anti-Tobacco mosaic virus (TMV) activities. The isolate was identified as Aspergillus tubingensis FJBJ11 based on morphological characteristics and ITS sequence. Bioassay-guided isolation led to the identification of a cycli penta-peptide, malformin A₁, along with two cyclic dipeptides, cyclo (Gly-l-Pro) and cyclo (Ala-Leu). Malformin A₁ showed potent inhibitory effect against the infection and replication of TMV with IC₅₀ values of 19.7 and 45.4 μg·mL⁻¹, as tested using local lesion assay and leaf-disc method, respectively. The results indicated the potential use of malformin A₁ as a leading compound or a promising candidate of new viricide.     

Diagnostic Potential of Differentially Expressed Homer1, IL-1β, and TNF-α in Coronary Artery Disease

Increasing evidences suggest that inflammation plays an important role in the pathogenesis of coronary artery disease (CAD). Numerous inflammatory cytokines and related genes mediate adverse cardiovascular events in patients with CAD, such as interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), and Homer in the present study. The study was carried out on 163 CAD patients at different stages and 68 controls. The gene expression of Homer1, Homer2, Homer3, IL-1β, and TNF-α in the peripheral blood leukocytes were measured by real-time polymerase chain reaction. The mRNA levels of Homer1, IL-1β, and TNF-α in CAD patients were significantly higher than those in the control group, but not Homer2 and Homer3. However, there was no considerable difference in the mRNA levels of Homer1, IL-1β, and TNF-α among AMI, UAP, and SAP three subgroups of CAD. The receiver operating characteristic (ROC) curves showed that Homer1 had a better diagnostic value for UAP patients compared with IL-1β and TNF-α. Like IL-1β and TNF-α, Homer1 may also be an important participant of atherosclerotic plaque development and eventually rupture. The results of the present study may provide an important basis for diagnosing CAD patients, and provide new therapeutic targets for CAD.     

Sinterability of Forsterite Prepared via Solid‐State Reaction

In this work, the sinterability of forsterite powder synthesized via solid‐state reaction was investigated. X‐ray diffraction (XRD) analyses indicate that the synthesized powder possessed peaks that correspond to stoichiometric forsterite. Scanning electron micrographs revealed that the powders were formed agglomerates, which were made up of loosely packed fine particles. Subsequently, the forsterite powders were cold isostatically pressed into a disk shape under 200 MPa and sintered in air at temperature ranging from 1200°C to 1500°C (interval of 50°C) with ramp rate of 10°C/min and dwelling time of 2 h. The sinterability of each sintered samples was examined in terms of phase stability, relative density, Vickers hardness, fracture toughness, and microstructural examination. XRD examination on all the sintered samples exhibited pure forsterite, in which the generated peaks were found to be in a good agreement with JCPDS card no. 34‐0189. The densification of forsterite progressed to reach a maximum relative density of ~91% at 1500°C. This study also revealed that high‐strength forsterite ceramic can be synthesized via solid‐state reaction as forsterite attained favorable mechanical properties, having fracture toughness of 4.88 MPam^1/2 and hardness of 7.11 GPa at 1400°C.     

Microstructure of isotactic polypropylene obtained using Ziegler–Natta catalyst at high polymerization temperature

The microstructure of the isotactic polypropylene obtained with various MgCl₂‐supported catalyst systems at high polymerization temperature of 70–100°C is investigated by discussing the intrinsic relation between the different types of active centers and the polymerization temperatures via gel permeation chromatography, temperature rising elution fractionation, and ¹³C NMR. For the MgCl₂/TiCl₄/di‐n‐butyl phathalate‐AlEt₃/external donor and MgCl₂/TiCl₄/2,2‐diisobutyl‐1,3‐dimethoxypropane‐AlEt₃ catalyst systems, the differences in the isotactic productivity of polymers obtained at different polymerization temperatures mainly result from the variation of both the activity of the different isospecific active centers and the stability constants of the complex of catalyst/donor. The reaction rate of high isotactic active centers reaches maximum at 85–90°C, and this effect contributes to both the highest isotacticity and the narrowest molecular weight distribution. For the MgCl₂/TiCl₄/phthalate ester‐AlEt₃ catalyst system, the isotacticity of polypropylene remains approximately constant in the temperature range of experiments, which could be ascribed to elution of phthalate ester after the activation. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42487.