Effects of the dietary protein to energy ratio on growth,feed utilization and body composition in Macrobrachium nipponense

Oriental river prawn (Macrobrachium nipponense) has been widely cultured in Asian countries. However, its nutritional studies are very limited. In the present 8‐week study, we investigated the effects of dietary protein to energy ratio (P/E ratio) on the growth, feed utilization and body composition in juvenile M. nipponense (initial weight 0.302 ±0.03 g). Two‐factor experiment was designed and nine semi‐purified diets were formulated to contain three lipid levels (20, 80 and 140 g kg^?1) and three protein levels (330, 380 and 430 g kg^?1), producing P/E ratios from 16.5 to 23.4 mg KJ^?1 protein. The results indicated that the growth, survival rate and protein efficiency were dose dependently improved by the increased dietary lipid, but not dietary protein content. Increased dietary lipid content and/or protein content increased lipid accumulation in whole body, hepatopancreas and muscle, but did not change the feed intake and hepatopancreas weight. In conclusion, our present study indicated that M. nipponense is a species with relatively high‐energy requirement. It could utilize dietary lipid content up to 140 g kg^?1, while the dietary protein with more than 330 g kg^?1 would not promote growth and protein efficiency. Taken together, 330 g kg^?1 dietary protein and 140 g kg^?1 dietary lipid level with P/E ratio 16.49 could be optimum for M. nipponense.     

Effect of high inclusion of rendered animal by‐product ingredients on growth,digestibility and economic performances in climbing perch Anabas testudineus

A 70‐day growth trail was conducted to investigate the effects of inclusion of high levels of meat and bone meal (MBM) and protein concentrate (PC) on growth, digestibility and economic performances of climbing perch, Anabas testudineus. Four isonitrogenous diets were formulated by lowering the level of dietary fishmeal protein at 0 (D₁, control), 70 (D₂), 85 (D₃) and 100% (D₄) with a mixture of MBM and PC protein (1:1). Triplicate groups of 300 fish (mean weight of 0.80 g) stocked in each 40 m² pond and fed the respective test diets. A digestibility trial was conducted after the growth trial in indoor glass aquarium. The result showed that growth parameters were significantly decreased (P < 0.05) with fishmeal replacement levels. However, significant differences were not found in feed conversion ratio and survival of fish. No difference was also found in protein efficiency ratio among D1, D2 and D3. Similar to growth parameters, total fish production was highest in D1, intermediate in D2 and D3; and lowest in D4. Apparent digestibility coefficients of dry matter, protein and lipid were highest (P < 0.05) in D1 and lowest in D4. The economic analysis revealed that the benefit cost ratio was ranked by D₃ (1.81), D₂ (1.71), D₁ (1.66) and D₄ (1.46) respectively. Upon considering the overall performances and unavailability of finite protein sources, it can be concluded that 70–85% fishmeal could be replaced with a mixture of MBM and PC (1:1) in practical diets for climbing perch.     

Detect unique molecular structure associated with physiochemical properties in CDC varieties of oat grain with unique nutrient traits [Feed Type vs. Milling Type] in comparison with barley grain using advanced molecular spectroscopy as a non-destructive biological tool

The objective of this study was to determinate grain unique protein inherent molecular structure that are related physiochemical and nutrient profiles in CDC developed oat varieties [CDC Nasser (Feed Type) and CDC Seabiscuit (Milling Type)] grown in cool climate condition in western Canada in comparison with conventional barley variety of CDC Meredith as a control using advanced molecular spectroscopy. Multivariate analyses, including an agglomerative hierarchical cluster analysis (CLA) and principal component analysis (PCA), were performed to identify protein molecular structural differences among the grains. The results revealed that CDC Seabiscuit contained greater (P < 0.05) protein structural Amide I and II than CDC Nasser and CDC Meredith, while the greater (P < 0.005) structural Amide I to II area and height ratios was detected in CDC Meredith. New oat grains had greater (P < 0.05) β-sheet height than barley grains, however, there was no difference in α-helix to β-sheet ratio values among the varieties. In conclusion, CDC Nasser and CDC Meredith had no difference in protein molecular structural features, while CDC Seabiscuit contains different protein structural characteristics as compared to CDC Meredith grain. The molecular structure features are highly associated with physiochemical and nutrient profiles in grains, which indicate that it also affect nutrient utilization and availability.     

Impacts of diet on hindgut microbiota and short‐chain fatty acids in grass carp (Ctenopharyngodon idellus)

Diet is known to influence intestinal microbiota in fish, but the specifics of these impacts are still poorly understood. Different protein/fibre ratio diets may result in differing structures and activities of gut microbiota. We examined the hindgut microbiome of grass carp (Ctenopharyngodon idellus) fed three different diets: fish meal (FM, high protein – low fibre), Sudan grass (SG, high fibre – low protein) and compound feed (CF, intermediate). Microbial profiles of fish fed on FM were significantly different from profiles of fish fed CF and SG (F = 18.85, p < .01). Cetobacterium, known to be positively associated with protein digestion, was the dominant microbial group in FM samples (approximately 75.7%), while Lachnospiraceae and Erysipelotrichaceae, thought to be involved in fermentation of plant polysaccharides, were dominant in CF and SG samples (46.8% and 42.9% respectively). Network analyses indicated that the abundance of Lachnospiraceae and Erysipelotrichaceae was in a significantly positive correlation (r = .895, p = .001). Short‐chain fatty acid (SCFA) levels may indicate that the digestibility of diet by microbiota in the grass carp gut decreased from FM to SG (FM>CF>SG). Overall low SCFA levels indicate that hindgut fermentation probably provides a low proportion of energy requirements in grass carp.     

基于YOLO v3与图结构模型的群养猪只头尾辨别方法

在利用视频监控技术对群养猪只进行自动行为监测时,对猪只准确定位并辨别其头尾位置对提高监测水平至关重要,基于此提出一种基于YOLO v3(You only look once v3)模型与图结构模型(Pictorial structure models)的猪只头尾辨别方法。首先,利用基于深度卷积神经网络的YOLO v3目标检测模型,训练猪只整体及其头部和尾部3类目标的检测器,从而在输入图像中获得猪只整体及头尾部所有的检测结果;然后,引入图结构模型,描述猪只的头尾结构特征,对每个猪只整体检测矩形框内的头尾部位组合计算匹配得分,选择最优的部位组合方式;对部分部位漏检的情况,采取阈值分割与前景椭圆拟合的方法,根据椭圆长轴推理出缺失部位。在实际猪场环境下,通过俯拍获得猪舍监控视频,建立了图像数据集,并进行了检测实验。实验结果表明,与直接利用YOLO v3模型相比,本文方法对头尾定位的精确率和召回率均有一定提高。本文方法对猪只头尾辨别精确率达到96.22%,与其他方法相比具有明显优势。     

玉米空间分层施肥装置结构优化与试验

针对玉米分层施肥作业中开沟宽度大、回土效果差导致的肥料分层效果不明显、各层肥量难以控制等问题，设计了一种各层肥量可调的空间分层施肥装置，肥料可在土壤中形成半包围种子的分布状态。通过理论分析和设计计算确定了空间分层施肥装置的基本结构参数，明确了影响分层施肥装置内肥料颗粒运动的主要因素。运用离散元法对分层施肥装置工作过程进行仿真分析，选取施肥调节片前端宽度、后端宽度和安装角为试验因素，以上层和中层排肥口出肥量为试验指标，进行二次正交旋转组合仿真试验，建立了试验指标与影响因素的回归模型，仿真结果表明，当施肥调节片前端宽度为3.61mm，后端宽度为21.52mm，安装角为43.23°时，上、中、下3层排肥口施肥量比例为最佳施肥比例3∶3∶4。为验证仿真分析结果，在不同作业速度和不同施肥量条件下，进行了空间分层施肥装置的样机性能试验，试验结果表明，空间分层施肥装置能够实现各层肥量的目标施肥配比，在不同作业速度和不同施肥量下各层施肥量变异系数不大于4.3%，各层肥料深度误差在10mm以内，各层肥料横向距离误差在6mm以内，工作性能稳定。     

木尔坦棉花曲叶病毒编码蛋白的亚细胞定位分析

 木尔坦棉花曲叶病毒(Cotton leaf curl Multan virus,CLCuMV)是典型的单组分双生病毒,并伴随β卫星分子,是棉花曲叶病的主要病原之一。本研究利用农杆菌介导的瞬时表达系统,将CLCuMV及其卫星分子编码的7个病毒蛋白在本氏烟表皮细胞中表达。通过激光共聚焦显微镜观察发现:V1、C2和C3定位于细胞核;C1和βC1定位在细胞核以及细胞质或细胞膜上,并且在细胞质中形成丝状结构;V2和C4主要定位在细胞质或细胞膜上,细胞核也有微量表达,V2可形成大小不一的颗粒状聚集体结构,C4在细胞膜上可见点状聚集体结构。同时,利用RT-PCR和Western blot对病毒各基因的转录和表达水平进行了分析。CLCuMV编码蛋白的亚细胞定位为蛋白功能的进一步研究提供重要理论依据。     

病程相关蛋白在采后果蔬诱导抗病性中的研究进展

果蔬受到真菌、细菌或病毒侵染时,自身能诱导产生病程相关蛋白(Pathogenesis-related proteins,PRs)。根据它们的结构亲缘关系和生物活性,PRs被分为17个功能家族。在控制果蔬采后病害的研究中,利用激发子诱导产生果蔬抗性已逐渐成为果蔬采后病害防治中一种安全、高效的保鲜方法,这也成为果蔬采后抗病研究的热点和发展趋势。本文综述了果蔬病程相关蛋白的分类、功能、诱导表达,以及蛋白组学技术在果蔬采后PRs表达水平上的应用,以期为果蔬病程相关蛋白的研究提供借鉴和参考。     

木薯(Manihot esculenta)AKT1基因的克隆及生物信息学分析

植物细胞中的K^+通道蛋白AKT1(Arabidopsis K^+transpoter 1)主要负责吸收K^+。本研究基于木薯基因组数据库信息,利用PCR技术从木薯中克隆一个MeAKT1基因,该基因全长2634 bp,编码877个氨基酸,生物信息学分析表明MeAKT1含有10个外显子和9个内含子,编码的氨基酸分子量为99.02 kD,等电点为8.43,属于稳定蛋白。MeAKT1包含有5个跨膜区域,N端含有1个Ion_trans结构域,C端有1个KHA结构域,其二级结构以α-螺旋和无规则卷曲为主,进化树分析发现MeAKT1与蓖麻RcAKT1的亲缘关系最近。通过对MeAKT1蛋白的生物信息学分析有助于下一步深入研究MeAKT1在木薯耐贫瘠过程中的功能。     

MicroRNA-145 inhibits epithelial-mesenchymal transition in human renal cancer A-498 cells by ADAM28

AIM: To investigate the inhibitory effect of microRNA-145 (miR-145) on epithelial-mesenchymal transition (EMT) in renal cancer A-498 cells. METHODS: The A-498 cells were transfected with miR-145 mimics (M145) and mimic negative control(MNC), which served as M145 group and MNC group, respectively. Mock control (MC) group was set up using untreated A-498 cells. The expression level of miR-145 in each group was detected by RT-qPCR. Transwell assay was used to detect the invasion ability of the cells. The protein expression of vimentin, E-cadherin and ADAM28 was determined by Western blot. Bioinformatic method was used to predict the target genes of miR-145. Antagonistic effect of ADAM28 over-expression on the inhibition of EMT by miR-145 was detected by Western blot. The relationship between miR-145 and ADAM28 was analyzed by dual-luciferase reporter assay. RESULTS: The expression level of miR-145 in M145 group was significantly up-regulated than that in MC group (P<0.05). The number of invasive cells in M145 group was 12.78±3.37, which was significantly lower than that in MC group (P<0.05). ADAM28 may be the target gene of miR-145. Compared with MC group, the protein expression of vimentin and ADAM28 in M145 group was significantly decreased (P<0.05), while the protein expression of E-cadherin was significantly increased (P<0.05).After ADAM28 over-expression, the protein expression of vimentin in the A-498 cells of M145 group was significantly increased (P<0.05), and the protein expression of E-cadherin was significantly decreased (P<0.05). The results of dual-lucife-irasei reporter assay showed that ADAM28 was a downstream target gene of miR-145. CONCLUSION: miR-145 may inhibit the expression of EMT-related proteins through the downstream target gene ADAM28 and inhibit the EMT process of renal cancer A-498 cells.