猪GRP78基因克隆、生物信息学分析及组织表达谱研究

本研究旨在克隆猪葡萄糖调节蛋白78（glucose-regulated protein 78，GRP78）基因，并进行生物信息学分析，探讨其在猪不同组织中的表达情况。根据GenBank上公布的猪GRP78基因序列（登录号：XM_001927795.6）设计引物，PCR扩增及测序获得猪GRP78基因CDS序列，使用在线软件分析GRP78的理化性质、跨膜结构、信号肽、疏水性、保守结构域、二级结构和三级结构，并进行同源性比对及系统进化树构建，利用实时荧光定量PCR方法检测猪GRP78基因在各组织中的表达情况。结果显示，猪GRP78基因CDS区长1 965 bp，可编码654个氨基酸。生物信息学分析表明，GRP78理论分子质量为72.3 ku，等电点（pI）为5.06，半衰期为30 h，其水溶液在280 nm处的消光系数为30 495，肽链N端为蛋氨酸（Met），不稳定系数为32.39，属于稳定蛋白。脂肪系数为85.40，总平均疏水指数为-0.496，无跨膜结构，存在信号肽序列，说明该蛋白属于分泌型蛋白；GRP78蛋白只包含1个超家族保守结构域：HSP70结构域。蛋白二级结构分析显示，GRP78蛋白中α-螺旋、延伸链、β-转角和无规则卷曲分别为40.06%、20.49%、8.10%和31.35%。同源性比对结果显示，猪GRP78基因与人（登录号：NM_005347.4）、小鼠（登录号：NM_001163434.1）、大鼠（登录号：NM_013083.2）、山羊（登录号：XM_005687138.3）、牛（登录号：NM_001075148.1）核苷酸序列的同源性分别为93%、91%、90%、95%、95%，氨基酸序列的同源性分别为99%、98%、98%、99%、99%，各个物种之间GRP78基因保守性较高。实时荧光定量PCR结果显示，GRP78基因在心脏、肝脏、脾脏、肺脏、肾脏、小肠、胃、卵巢、输卵管、乳腺、小脑、大脑、垂体等组织中均有表达，在心脏、脾脏、肺脏中相对高表达。本研究结果为今后深入研究GRP78基因的生物学功能提供了基础材料。     

Liver histology and histomorphometry in hybrid sorubim (Pseudoplatystoma reticulatum × Pseudoplatystoma corruscans) reared on intensive fish farming

This study aimed to characterize the liver histology and histomorphometry in sorubim hybrid of different categories (nursery, growth and grow‐out) reared on fish farming. The categories were defined considering body weight (BW): nursery category (n = 5): BW = 37.06 ± 6.00 g (31.6–45.3 g); growth category (n = 5): BW = 310.40 ± 53.80 g (242.1–376.4 g) and grow‐out category (n = 5): BW = 874.28 ± 27.59 g (846.2–913.1 g). Liver fragments were processed to paraffin inclusion, and sections were stained by haematoxylin and eosin (H&E), PAS (Periodic Acid Schiff) and Perl's staining to histology, histomorphometry and density volumetric of liver structures; glycogen analysis and to detect ferric irons (Fe³⁺) respectively. The hepatosomatic index decreased between the categories (P < 0.01). The percentage of PAS‐positive hepatocytes in the nursery category was higher (P < 0.05) in relation to the growth and grow‐out categories. The hepatocytes from all fish were positive to Perl's staining. The density volumetric of liver structures did not differ among categories except to blood vessels were higher (P < 0.01) in the nursery and growth. The area (μm²) and perimeter (μm) of hepatocytes, and the area (μm²), perimeter (μm) and volume (μm³) of the nuclei from grow‐out fish were lower (P < 0.01) than those from the nursery and growth categories. Changes in morphometric characteristics of hepatocytes may result from metabolic changes associated with body growth surubins; therefore, these morphometric characteristics of liver tissue can be used as functional biomarkers for the assessment of fish health and nutrition status.     

The effects of diet supplemented with Lactobacillus rhamnosus on tissue parameters of rainbow trout,Oncorhynchus mykiss (Walbaum)

This study was carried out to establish the effects of a 6 week treatment with the diet supplemented with L. rhamnosus in concentrations of 10⁷ CFU g^?1 (G1 group) and 10⁸ CFU g^?1 (G2 group) on the condition expressed by condition factors (Fulton's, Clark's and B), intestinal microbiology, haematological, histological and selected antioxidative parameters of rainbow trout. A significantly higher condition factors were found in G1 group indicating that higher concentration of probiotic (10⁸ CFU g^?1) did not result in the better condition. Cholesterol and urea levels were significantly higher in both G1 and G2 groups, albumin in G1 and creatinine in G2 group with respect to control. A significantly higher liver TBARS level was observed in G2 group. The feeding with supplemented probiont apparently changed the resident microbiota. Three weeks after withdrawal of the supplemented feed, the microflora mostly reverted to the control composition, although L. rhamnosus in faecal matter of fish remained inherent. The epithelial structure of the proximal and distal intestine revealed the increased absorptive area in both treated groups, as well as the increase in the mucin‐secreting goblet cells. The L. rhamnosus‐treated groups demonstrated the capacity for the augmentation of the innate host defence.     

实木家具的拆装式结构实现路径探究

遵循结构合理、体积缩小、组装方便、外形美观的设计原则,从拆装式节点实现形式、整体结构拆装方式二个维度系统阐述了实木家具拆装结构实现路径,并对榫自锁可拆式、连接件可拆式两种实木家具拆装式节点形式及椅类、桌台类、柜类、床类家具的整体结构可拆装方式进行了详细介绍,以期为实木家具的结构优化及平板化包装提供思路。     

牦牛CRH基因克隆及其在生殖轴中的表达研究

为了探讨促肾上腺皮质激素释放激素（corticotropin-releasing hormone，CRH）基因在牦牛繁殖中的调控作用，试验分别采集5头成年母牦牛和5头成年母黄牛的下丘脑、脑垂体前叶、输卵管、卵巢和子宫等组织，通过RT-PCR技术及生物信息学软件对牦牛CRH基因编码区进行扩增、克隆及序列分析，并构建系统进化树；采用实时荧光定量PCR法检测CRH基因的组织表达。结果表明，牦牛CRH基因编码区全长573 bp，编码190个氨基酸。牦牛与黄牛、猫、鸡、人、小鼠、大鼠和猪的CRH基因核苷酸同源性分别为99.8%、43.3%、36.1%、46.2%、39.0%、38.5%和56.4%。系统进化树表明，牦牛与黄牛亲缘关系最近，并与其他物种类聚，符合物种进化规律。CRH蛋白分子式为C₉₂₀H₁₅₀₃N₂₇₉O₂₆₃S₃，分子质量为20776.95 u，理论等电点为10.95，其氨基酸组成中亮氨酸（L）、脯氨酸（P）、丙氨酸（A）和精氨酸（R）所占比例较高，分别为15.8%、12.6%、12.1%和10.5%。CRH蛋白为不稳定亲水蛋白，存在信号肽和跨膜结构。CRH蛋白二级结构中α-螺旋、β-转角、延伸链和无规则卷曲分别占41.05%、1.05%、8.42%和49.48%，三级结构分析结果与其相一致。CRH基因mRNA在牦牛下丘脑中表达量最高，显著高于其他组织（P<0.05），在子宫中表达量最低。牦牛脑垂体前叶CRH基因mRNA表达量极显著高于黄牛（P<0.01），在卵巢、输卵管中表达量显著高于黄牛（P<0.05），而两个品种在下丘脑、子宫中的表达量差异不显著（P>0.05）。提示CRH基因在牦牛繁殖调控中具有重要作用。     

促进绿色未来的全球木材科学与技术研究进展——国际林联第25届世界大会木材议题综述

国际林业研究组织联盟（IUFRO）第25届世界大会于2019年在巴西召开。文中从木材生长、木材性质与质量、木材识别、木材加工利用和木文化5个方面分别论述了这次大会在木材科学与技术领域的国际最新研究热点与进展，以反映全球木材科学的研究现状，并梳理学科发展方向。木材形成、木材质量、木材高附加值利用、木材识别新技术等议题依然是木材科学与技术领域的未来研究热点。     

基于GC-MS顶空进样法鉴别瘿木降香黄檀与大果紫檀

分别对两个批次含瘿瘤的降香黄檀和大果紫檀木材,采用GC-MS技术顶空进样方式,获取其总离子流图并进行相关系数、系统聚类和特征性化学成分分析。结果表明:两种木材之间总离子流图差别大,无相关性,而同种木材不同批次间相似度高,均含有相同的特征峰,相关系数高(R>0.900);系统聚类分析进一步验证了该试验结果;两种含瘿瘤木材主要特征化学成分种类和含量也完全不同;相关性分析、聚类分析和特征性成分分析均可鉴别区分这两种含瘿瘤木材,解决了含瘿瘤木材传统方法难以鉴别的难题。