饲用酵母甘露聚糖检测方法研究进展

酵母细胞中的甘露聚糖是一种非淀粉多糖,存在于酵母细胞壁的外层中。酵母甘露聚糖通常与蛋白质以共价键的形式相连,被称为甘露糖蛋白。酵母甘露聚糖在动物营养中具有重要的生物学功能,是酵母源生物产品中的关键功能性成分之一。甘露聚糖含量是评价酵母提取物、酵母水解物、酵母培养物等产品品质的重要指标。本文就饲用酵母甘露聚糖的检测方法研究进展做一综述。     

富锗酵母培养物对下笼蛋鸡肉品质、肠道菌群及结构的影响

本试验旨在研究富锗酵母培养物对下笼蛋鸡肉品质及肠道的影响。选取505日龄健康的海兰褐壳蛋鸡480只,随机分为4组,每组5个重复,每个重复24只鸡。对照组饲喂基础日粮,试验组在基础日粮中分别添加12、16、20 mg/kg的富锗酵母菌培养物。预试期7 d,正试期为42 d。结果表明:与对照组相比,12、16、20 mg/kg组腿肉的蒸煮损失分别降低45.2%、33.6%、39.7%(P<0.01),pH均高于对照组(P<0.01);16mg/kg组腿肌的亮度(L~*)低于对照组(P<0.05);12、16、20 mg/kg组腿肌的剪切力分别比对照组低44.13%、56.07%、50.60%(P<0.01);各试验组胸肌pH均高于对照组(P<0.01),16mg/kg组的pH高于12、20mg/kg组(P<0.05);与对照组相比,16mg/kg组乳酸菌数量升高(P<0.05);空肠中,各试验组的绒毛长度高于对照组(P<0.01);16、20 mg/kg组绒毛长度/隐窝深度高于对照组(P<0.01)。结果显示,日粮中添加富锗酵母培养物可以改善下笼蛋鸡小肠的形态结构和肠道菌群平衡,提高鸡肉品质,建议添加量为16 mg/kg。     

Effect of Partial Replacement of Steam Rolled Corn With Soybean Hulls or Prickly Pear Cactus in the Horse's Diet in the Presence of Live Saccharomyces cerevisiae on In Vitro Fecal Gas Production

The aim of the study was to evaluate the fecal fermentation of partial replacing steam rolled corn with soybean hulls (SH) or prickly pear cactus (PC) as energy source in horse diets, in the presence of Saccharomyces cerevisiae. Steam rolled corn was replaced with SH at 0% (control), 7.5% (SH75), and 15% (SH150) in the first trial, whereas it was replaced with PC at 0% (control; the same of the first trial), 7.5% (PC75), and 15% (PC150) in the second trial. Yeast of S. cerevisiae was added at 0, 2, and 4 mg/g dry matter (DM) of incubated substrates. Fecal inoculum was obtained from four adult English Thoroughbred horses fed on an amount of commercial concentrate and oat hay ad libitum. Interactions observed between PC rations and yeast doses for the asymptotic gas production (GP), the rate of GP and carbon dioxide (CO₂) production during some incubation hours. Moreover, with no effect due to SH rations (P > .05), increased (P < .05) rate of GP was observed with the ration PC75 compared with other rations. Besides, PC75 and PC150 rations with 0 mg yeast/g DM linearly decreased (P < .05) CO₂ production at some incubation hours. However, SH75 and SH150 ration had increased (P = .005) DM degradability (DMD). Yeast addition at 2 mg/g DM increased the asymptotic GP (P = .048) with the SH75 and PC150 rations. The level of 4 mg yeast/g DM increased the asymptotic GP (P = .048) from the SH150 ration. Yeast addition at 2 and 4 mg/g DM increased (P < .05) ​the asymptotic GP from PC75 and PC150 rations, respectively, with increasing DMD with the both doses. Yeast addition increased (P < .05) CO₂ production from SH75, SH150, PC75, and PC150 rations. It could be concluded that SH and PC can replace steam rolled corn at levels of 7.5% to 15% without negative effect of fermentation kinetics and with better fermentation performance in the presence of yeast at 2 mg/g DM of substrates.     

大肠杆菌表达系统和酵母表达系统的研究进展

由于DNA重组技术和蛋白组技术的发展与成熟,外源基因表达技术备受关注。其在生物、食品、工业以及医学领域发挥着举足轻重的作用。以原核生物细胞及真核生物细胞作为表达系统,进行目的基因序列的表达以生产蛋白疫苗、核酸疫苗和生物酶制剂等是近年来发酵工业的新型领域。原核和真核表达系统是近年来研究和应用最广泛和最成熟的外源基因表达系统。对近年来关于大肠杆菌表达系统和酵母表达系统的研究进展进行了综述。     

Interaction of NR2D subunit of NMDA receptor with MOCA

AIM: To identify the potential proteins interacting with NR2D subunit of NMDA receptor by yeast two-hybrid screening and to investigate the role of NR2D in excitotoxicity of the retina.METHODS: The Clontech GAL4 yeast two-hybrid system was used to screen the mouse brain cDNA library, and the bait plasmid containing C-terminus of NR2D was constructed. Physical interaction between 2 proteins was verified by co-immunoprecipitation assay. The subcellular localization of 2 proteins in the mouse retina was observed under microscope with immunofluorescence.RESULTS: Modifier of cell adhesion (MOCA) was identified as a new protein interacting with NR2D. MOCA and NR2D were co-expressed in the mouse retina. CONCLUSION: MOCA specifically interacts with NR2D, which provides the experimental basis for identifying the role of glutamate excitotoxicity in the retina neurodegeneration.     

巴西橡胶树乳管细胞HblMYC3互作蛋白筛选与功能分析

MYC是b HLH转录因子家族的亚家族成员,在植物茉莉酸信号转导过程中发挥着重要的调节作用。Hbl MYC3是从巴西橡胶树的乳管细胞中分离鉴定到的MYC类转录因子,其基因表达受割胶和茉莉酸上调。采用酵母双杂交方法初步筛选Hbl MYC3蛋白的互作蛋白,旨在进一步了解Hbl MYC3的功能。结果表明:Hbl MYC1、Hbl MYC2、DNAJ蛋白、谷氧还蛋白2、含A20和AN1锌指结构域的胁迫相关蛋白5、28 ku热和酸稳定的磷蛋白以及25 ku泛素连接酶E2等7种蛋白不同程度地与Hbl MYC3蛋白互作。基于这些互作蛋白的功能,推测Hbl MYC1或Hbl MYC2通过与Hbl MYC3形成二聚体对小橡胶粒子膜蛋白基因表达进行调控,其他蛋白参与胁迫条件下维持二聚体的稳定性和胁迫反应后降解该二聚体。     

酸马奶中酵母菌部分代谢特性的研究

对锡盟地区马奶酒中分离的11株酵母菌的代谢特性进行了研究。研究内容包括:酵母菌对蛋白质利用能力及酵母菌对脂肪利用能力。采用OPA法,考查了蛋白酶的活力,通过测定酵母菌中蛋白酶对乳中酪蛋白的利用,反映酵母菌对蛋白质的代谢情况;采用平板扩散法,考查了脂肪酶的活力,通过观测透明圈直径的大小来反映酵母菌对脂肪的代谢情况。     

小麦转录因子TaMYB5 like转录自激活能力及其参与生理型花粉败育过程表达模式研究

化学杂交剂SQ-1诱导的小麦花粉败育是一个复杂的生理代谢过程，TaMYB5-like被发现参与此过程。为了解TaMYB5-like基因在SQ-1诱导小麦生理型花粉败育过程中的作用，以SQ-1诱导的小麦生理型雄性不育系PHYMS-1376和对照可育系CK-1376四分体、单核早期、单核晚期、二核期和三核期花药为试验材料，克隆TaMYB5-like基因，并对其进行序列结构、生物信息学、表达模式、亚细胞定位及转录自激活效应分析。结果发现，TaMYB5-like基因序列长5 207 bp，其cDNA长为1 133 bp，其中CDS序列长819 bp，编码272个氨基酸，含有2个SANT结构域，分子量为29.36 kDa，无信号肽，无跨膜结构，亚细胞定位在细胞核内；TaMYB5-like基因启动子涉及光响应、逆境胁迫响应、茉莉酸甲酯响应等顺式作用元件。自激活效应发现，TaMYB5-like蛋白的自激活区段位于N端，合适浓度的AbA和3-AT可以抑制BD-TaMYB5-like和BD-TaMYB5-like-N-SANT融合蛋白的自激活性；随着蛋白质氨基酸序列的截断，自激活性呈降低趋势。与CK-1376相比，PHYMS-1376四分体和单核早期花药中TaMYB5-like表达量差异不显著；花药发育到单核晚期、二核期和三核期时，TaMYB5-like表达量显著增加；CK-1376和PHYMS-1376三核期时花药内TaMYB5-like表达量均最高。     

酵母蛋白饲喂泌乳奶牛试验报告

本试验通过在荷斯坦泌乳牛日粮中添加酵母蛋白部分替代豆粕,研究其对泌乳牛干物质采食量、产奶量、乳成分及身体健康情况的影响,选取400头胎次、产奶量相近的中国荷斯坦泌乳牛分为对照组和试验组各200头,试验组每头牛每天饲喂500g酵母蛋白,通过60d的试验,结果表明试验组和对照组奶牛平均日产奶量差异不显著（P〉0.05）,分别为32.54kg/d与32.34kg/d。在产奶量不变的基础上,试验组平均干物质采食量降低1.7kg（DM）/d,产奶效率提高,与对照组相比差异极显著（P〈0.01）。     

两种奶牛功能性添加剂效果对比试验

选取泌乳期高产和低产奶牛各18头。高产和低产中各随机选取9头在日粮中添加纤维素复合酶,添加量为0．1kg／t精料;其余18头在日粮中添加酵母培养物,添加量为2kg／t精料。结果显示,高产组饲喂纤维素复合酶的奶牛试验期第35天时产奶量显著高于饲喂酵母培养物的奶牛（P=0．024）,低产组饲喂纤维素复合酶的奶牛试验期内产奶量呈稳步上升趋势;高产组饲喂纤维素复合酶的奶牛乳脂率在试验期28天显著高于同组中饲喂酵母培养物的奶牛（P=0．022）,乳蛋白率在试验第7天（P=0．044）和第28天（P=0．018）显著高于同组中饲喂酵母培养物的奶牛。