西北干旱灌区紫花苜蓿高产田施肥效应及推荐施肥量研究

为揭示紫花苜蓿氮、磷、钾肥效应,采用“3414”不完全正交回归设计,对紫花苜蓿氮、磷、钾肥合理配比施肥效应进行研究,同时对紫花苜蓿产量及蛋白总量进行肥效模型拟合。结果表明,氮、磷、钾对建植2年苜蓿产量的贡献为钾>磷>氮,对建植3年苜蓿产量的贡献为磷>钾>氮,建植2与3年苜蓿交互效应均表现为氮磷>氮钾>磷钾。氮、磷、钾对建植2年苜蓿蛋白总量的贡献为氮>钾>磷,对建植3年苜蓿蛋白总量的贡献为氮>磷>钾。建植2年苜蓿氮磷肥互作效应明显优于氮钾、磷钾互作;建植3年苜蓿氮磷、氮钾交互对苜蓿蛋白总量的增产效果明显大于磷钾交互。采用频度分析法,通过模拟寻优,得出建植2年紫花苜蓿目标产量大于平均产量17522kg·hm^-2时,优化施肥量为氮56.27~67.51kg·hm^-2、磷77.69~90.48kg·hm^-2、钾76.43~87.18kg·hm^-2;建植3年紫花苜蓿目标产量大于平均产量19234.1kg·hm^-2时,优化施肥量为氮46.75~57.66kg·hm^-2、磷80.15~92.28kg·hm^-2、钾57.79~69.74kg·hm^-2;建植2年紫花苜蓿目标蛋白总量大于平均2115kg·hm^-2时,优化施肥量为氮66.35~77.48kg·hm^-2、磷79.34~92.87kg·hm^-2、钾73.68~85.38kg·hm^-2;建植3年紫花苜蓿目标蛋白总量大于平均2656kg·hm^-2时,优化施肥量为氮68.44~79.50kg·hm^-2、磷72.74~85.96kg·hm^-2、钾50.68~61.61kg·hm^-2。     

一种适用于双向电泳的家蚕微孢子虫总蛋白的制备方法

本文对适用于双向电泳的微孢子虫总蛋白提取方法进行了探讨。研究表明，采用液氮多次冻融结合手工研磨，再用裂解液抽提的方法能够得到产率较高且适用于双向电泳的家蚕微孢子虫总蛋白。     

动物繁殖激素产品现存的问题和创新

近年来,为了提高母猪的繁殖效率,满足养猪业养殖高度集约化的生产要求,行业内开始大力推广批次化生产繁殖技术。目前国内都是采用提取类生殖激素孕马血清(PMSG)和孕妇尿液中的人绒毛膜促性腺激素(HCG),以及化学激素烯丙孕素进行繁殖调控。但是这些提取类产品仍存在一些缺陷,因此开发出活性好、纯度高、成本低的高品质蛋白类繁殖激素产品,进而应用于猪场批次化生产中,是提高我国乃至全球畜牧业发展效率的关键所在。     

猪细小病毒NS基因原核表达与多克隆抗体制备

旨在制备抗猪细小病毒(PPV)非结构蛋白共有氨基酸的NS多肽多克隆抗体。根据GenBank(MK993540)公布的PPV基因组序列,克隆其非结构蛋白NS1、NS2共有基因序列(NS基因),并进行生物信息学分析。进而将NS基因克隆至原核表达载体pET-32a,构建重组质粒pET-32a-NS,转化至大肠埃希菌Rosetta(DE3)中进行诱导表达,利用镍柱亲和层析技术纯化表达的重组多肽,用重组多肽免疫Balb/c小鼠制备多克隆抗体。结果显示,PPV杨凌株NS基因长258bp,编码86个氨基酸的多肽,是具有亲水性的非跨膜NS多肽,具有大量的B细胞线性表位。NS多肽在37℃、0.8mol/L IPTG条件下,诱导6h有大量的可溶性表达。免疫印迹试验结果显示,该多肽具有较好的抗原性。用纯化NS多肽免疫小鼠后获得鼠抗NS多肽的血清抗体效价为1∶12800。用制备的NS多克隆抗体检测纯化的NS重组多肽及真核表达的NS1蛋白,均能检测出相应特异性条带,为进一步研究NS蛋白在PPV致病过程中的作用奠定了基础。     

Hematologic, biochemical, and protein electrophoretic values in captive tawny owls (Strix aluco)

BACKGROUND: The tawny owl (Strix aluco) is a protected species in Italy. Orphaned, injured, and ill owls often are sheltered and treated in rehabilitation centers, where hematologic and biochemical analyses would be helpful to evaluate and monitor the status of their health. OBJECTIVES: The major aim of this work was to assess hematologic and biochemical constituents together with protein electrophoretic fractions in healthy tawny owls. In addition, we compared laboratory methods for determining hemoglobin (Hgb), total protein, and albumin concentrations. METHODS: Heparinized blood samples were collected from 10 clinically healthy adult captive tawny owls between March 2001 and November 2003 for CBC, routine biochemical analysis, and protein electrophoresis. Alternate methods for Hgb (estimation as HCT/3 vs spectrophotometry), total protein (biuret vs refractometry), and albumin (bromcresol green vs electrophoresis) concentrations were compared in 34 samples from 16 unhealthy adult owls and 8 nestlings. RESULTS: Results were reported as mean, median, and range (minimum-maximum). Significant differences and poor concordance were observed between methods for Hgb, total protein, and albumin. CONCLUSIONS: Hematologic and plasma biochemical values in captive tawny owls may be useful in evaluating and monitoring the health of this species in captivity.     

Tumour necrosis factor stimulated gene 6 intrinsically regulates PD-L1 expressions in breast cancer cells,leading to modulation of tumour microenvironment

Recent studies have shown that tumour cells express tumour necrosis factor-inducible gene 6 (TSG-6) and its protein, which is known to play a key role in regulating excessive immune responses and proliferation and growth of mesenchymal stem cells (MSCs). It has not been confirmed whether the inhibition of TSG-6 for tumour cells can suppress tumour cell growth and regulate the activation of immune cells in the tumour microenvironment (TME). TSG-6-specific small interfering RNA was transfected into canine and human breast cancer cells (CIPp, CIPm and BT-20). TSG-6-down-regulated (siTSG-6) cells showed decreased cell proliferation, migration, and invasion abilities. Decreased mRNA expressions of NF-κB, STAT3 and Sox2, confirming that TSG-6 is an upper factor governing tumour growth and metastasis. Notably, siTSG-6 cells showed significantly decreased expression levels of CD44 and PD-L1. Direct and indirect co-culture of canine peripheral blood mononuclear cells (cPBMCs) and the siTSG-6 cells showed significant activation in M1 type macrophages and cytotoxic T cells. They also showed a tendency to decrease in the expression of CTLA-4 and increase in the expression of PD-1. In conclusion, this study suggests that the down-regulation of TSG-6 in breast cancer cells could not only suppress tumour growth and metastasis, and but also regulate TME. Since modulation of immune checkpoint proteins occurs in both tumour cells and immune cells, inhibiting TSG-6 and its protein within the TME could be novel therapeutic target for anticancer treatment.     

植物蛋白对干酪凝乳特性的影响

研究3种植物蛋白对干酪凝乳特性的影响,从而选出1种最佳的植物蛋白.从3种干酪的凝乳特性(凝乳时间、凝乳强度、乳清OD值)和干酪凝块的质构特性(弹性、黏聚性、咀嚼性)2方面进行对比分析,并对干酪凝块的感官品质进行模糊评判.结果表明:添加豌豆蛋白制得的干酪品质优于其他两种.     

Effects of the ruminal comminution rate and microbial contamination of particles on accuracy of in situ estimates of ruminal degradability and intestinal digestibility of feedstuffs

Effects of considering the comminution rate (k_c) and the correction of microbial contamination (using ¹⁵N techniques) of particles in the rumen on estimates of ruminally undegraded fractions and their intestinal digestibility were examined generating composite samples (from rumen‐incubated residues) representative of the undegraded feed rumen outflow. The study used sunflower meal (SFM) and Italian ryegrass hay (RGH) and three rumen and duodenum cannulated wethers fed with a 40:60 RGH to concentrate diet (75 g DM/kgBW^0.75). Transit studies up to the duodenum with Yb‐SFM and Eu‐RGH marked samples showed higher k_c values (/h) in SFM than in RGH (0.577 vs. 0.0892, p = 0.034), whereas similar values occurred for the rumen passage rate (k_p). Estimates of ruminally undegraded and intestinal digestibility of all tested fractions decreased when k_c was considered and also applying microbial correction. Thus, microbial uncorrected k_p‐based proportions of intestinal digested undegraded crude protein overestimated those corrected and k_c?k_p‐based by 39% in SFM (0.146 vs. 0.105) and 761% in RGH (0.373 vs. 0.0433). Results show that both k_c and microbial contamination correction should be considered to obtain accurate in situ estimates in grasses, whereas in protein concentrates not considering k_c is an important source of error.     

Dietary supplementation of Zingiber officinale and Zingiber zerumbet to heat‐stressed broiler chickens and its effect on heat shock protein 70 expression,blood parameters and body temperature

The present study was conducted to assess the effects of dietary supplementation of Zingiber officinale and Zingiber zerumbet and to heat‐stressed broiler chickens on heat shock protein (HSP) 70 density, plasma corticosterone concentration (CORT), heterophil to lymphocyte ratio (HLR) and body temperature. Beginning from day 28, chicks were divided into five dietary groups: (i) basal diet (control), (ii) basal diet +1%Z. zerumbet powder (ZZ1%), (iii) basal diet +2%Z. zerumbet powder (ZZ2%), (iv) basal diet +1%Z. officinale powder (ZO1%) and (v) basal diet +2%Z. officinale powder (ZO2%). From day 35–42, heat stress was induced by exposing birds to 38 ± 1 °C and 80% RH for 2 h/day. Irrespective of diet, heat challenge elevated HSP70 expression, CORT and HLR on day 42. On day 42, following heat challenge, the ZZ1% birds showed lower body temperatures than those of control, ZO1% and ZO2%. Neither CORT nor HLR was significantly affected by diet. The ZO2% and ZZ2% diets enhanced HSP70 expression when compared to the control groups. We concluded that dietary supplementation of Z. officinale and Z. zerumbet powder may induce HSP70 reaction in broiler chickens exposed to heat stress.     

附睾中脂质运载蛋白家族的研究进展

脂质运载蛋白(lipocalin,Lcn)家族的功能十分重要,其中附睾分泌的Lcn家族能结合一些小分子配体,呈高度区域性分布,参与很多生物调控过程,在精子成熟过程中扮演重要角色,可为研究附睾功能提供理论基础。作者介绍了Lcn家族的结构特征、Lcn在附睾中的表达、作用及研究现状。