酵母培养物对反刍动物作用的研究进展   总被引：1，自引：0，他引：1  

张鹏飞  于安乐  高巍 《吉林畜牧兽医》2007,28(6):17-20

本文就直接饲喂微生物——酵母培养物的概念,现阶段酵母培养物对反刍动物瘤胃环境作用的生理生化基础的相关研究进展,以及几种对酵母培养基的作用机理解释。另外又对酵母培养物对反刍动物作用效果及影响酵母培养物的因素等5个方面进行了概述。  相似文献   

酵母菌载纳米铁去除水中2,4,6–三氯酚的性能     

肖苗  石国荣  戴镇璇  曾双晴  刘也峰  余心结 《湖南农业大学学报(自然科学版)》2022,48(3):319-325

以酵母菌为载体,废弃烟叶提取物为还原剂,制备酵母菌载纳米铁(TB–Fe/SCNPs),并探究其去除水中2, 4, 6–三氯酚(2, 4, 6–TCP)的性能。结果表明：负载在酵母菌上的纳米铁为粒径(77.6±16.1) nm的球形颗粒;TB–Fe/SC NPs去除2, 4, 6–TCP主要包括吸附和氧化降解2种途径,符合拟二级反应动力学模型;溶解氧和羟自由基在TB–Fe/SC NPs氧化降解2, 4, 6–TCP中起重要作用;TB–Fe/SC NPs对2, 4, 6–TCP的去除率随温度的升高而增大,随2, 4,6–TCP初始浓度的增大而减少,而反应体系的pH值对TB–Fe/SCNPs去除2,4,6–TCP的影响较小;TB–Fe/SCNPs用量为1.0～3.0g/L时,2,4,6–TCP的去除率随TB–Fe/SCNPs用量的增大而增大;Fe3+、Mg2+、Ca2+和SO42–能促进TB–Fe/SCNPs去除2,4,6–TCP的反应,HPO42–、HCO3–和腐殖酸则对反应有抑制作用,而K+、NO3–和Cl–对2, 4, 6–TCP的去除影响不明显;TB–Fe/SC NPs能在室温下稳定...  相似文献   

饲料中添加酵母提取物对凡纳滨对虾免疫相关基因表达及抗菌机能的影响   总被引：2，自引：2，他引：2  

黄旭雄  罗词兴  危立坤  陈春燕  赵利斌  李桑  刘林林  曾蓓蓓 《水产学报》2014,38(12):2049-2058

为了评估饲料中添加酵母提取物对凡纳滨对虾免疫灵敏性和平衡性的相关基因表达的影响,以鱼粉含量为24.5%的基础饲料(对照组)及在基础饲料中添加2.5%酵母提取物的实验饲料,分别饲喂凡纳滨对虾56 d,检测两种饲料投喂的对虾在急性感染溶藻弧菌前后鳃组织Toll受体、IM D和溶菌酶mRNA表达量变化及感染后的对虾死亡情况。结果表明:摄食添加酵母提取物饲料的凡纳滨对虾鳃组织中Toll受体mRNA和溶菌酶mRNA表达量均显著高于对照组对虾(P0.05),IMD mRNA表达量与对照组无显著性差异(P0.05)。急性感染溶藻弧菌后,两组对虾鳃组织Toll受体、IMD和溶菌酶mRNA表达量随感染进程均出现显著变化,Toll受体、IMD和溶菌酶mRNA表达量峰值出现的时间分别为24、42和36 h,且摄食添加酵母提取物组对虾各基因的表达量峰值分别为对照组峰值的201.06%、481.46%和276.77%,均显著高于对照组对虾(P0.05)。摄食添加酵母提取物饲料组对虾鳃组织中Toll受体和IM D mRNA表达量在感染溶藻弧菌后12和24 h分别出现显著上调,而对照组对虾鳃组织中Toll受体和IMD mRNA表达量分别在感染弧菌后24和42 h才出现显著上调。两组对虾经溶藻弧菌人工急性感染后72 h内的累积死亡率无显著差异(P0.05)。实验表明,饲料中添加酵母提取物上调了溶藻弧菌感染前凡纳滨对虾Toll受体和溶菌酶mRNA的表达量,提早了溶藻弧菌感染后对虾Toll受体和IMD mRNA表达量上调时间,且增加了对虾Toll受体、IM D和溶菌酶mRNA表达量的峰值,在一定程度上提高了凡纳滨对虾免疫相关基因表达的灵敏性。  相似文献   

Mass Production of Freshwater Rotifer,Brachionus calyciflorus,Under Different Diets and Regimes     

《Journal Of Applied Aquaculture》2013,25(3):101-111

ABSTRACT

The production ability of freshwater rotifer, Brachionus calyciflorus, cultured with two algal species, Chlorella vulgaris, and Spirulina platensis, and a baker's yeast, Saccharomyces cerevisiae, were studied using semicontinuous culture method. B. calyciflorus was fed with the above three types of food at five different concentrations (125, 250, 500,750, and 1,000 μg/mL). Among the three different types of diet, maximum production of B. calyciflorus (489.20 ±10.91 individuals/mL; P < 0.05) was obtained with C. vulgaris, followed by S. cerevisiae, and S. platensis. Moreover, in each of the three diets, the maximum rotifer production was obtained at a particular concentration (C. vulgaris, 750 μg/mL; S. cerevisiae, 750 μg/mL; and S. platensis, 500 μg/mL) beyond which the rotifer production decreased. The peak production due to C. vulgaris (489 individuals/mL) was better than S. cerevisiae (321 individuals/mL) when the number of rotifers was considered. The present study indicates that the quantity and quality of food have a significant role on the rotifer production and that C. vulgaris at 750 μg/mL appears suitable to feed to rotifers for maximal production.  相似文献   

光合细菌配合面包酵母与藻粉培养轮虫的实验   总被引：2，自引：0，他引：2  

姚雪梅  兰珍贵王鑫 《齐鲁渔业》2003,20(6):31-33

以面包酵母与一定量螺旋藻粉培养褶皱臂尾轮虫的过程中，添加光合细菌液进行实验。结果表明：光合细菌作为辅助性饵料，对轮虫的生长具有明显特殊的促进作用。4组实验显示：投喂适宜量光合细菌轮虫增殖明显加快，但与光合细菌添加量的增加不完全呈正比关系；投喂光合细菌新鲜培养液与老培养液轮虫增殖效果相近；投喂光合细菌只能作为辅助性饵料。当配合酵母、藻粉培育轮虫时，3者在饵料上起到了良好的互补作用，培养效果最佳。  相似文献   

三种免疫添加剂对草鱼非特异性免疫功能的影响   总被引：2，自引：0，他引：2  

于翔  李赫  宋文华  富丽静  姚福向  胡宗云  张涛  张健 《水产养殖》2011,32(7):38-43

在饲料中添加不同剂量的Vc、酵母多糖和壳聚糖,连续投喂42d,并在试验的第14、28、35和42天取样检测,研究其对草鱼血清溶菌酶活性、血清超氧化物歧化酶活性（SOD）活性、血清碱性磷酸酶（AKP）活性、补体C3、含量丙二醛（MDA）含量和血液白细胞吞噬活性共6种指标的影响。结果显示：实验组与对照组相比,饲料中添加Vc可以提高血清溶菌酶活性、SOD活性、AKP活性、补体C3含量和血液白细胞吞噬活性高,并降低MDA含量。添加酵母多糖可以提高血清溶菌酶活性、AKP活性、补体C3含量和血液白细胞吞噬活性,并降低MDA含量,但不能提高SOD活性。添加壳聚糖可以提高血清溶菌酶活性、SOD活性、AKP活性、补体C3含量和血液白细胞吞噬活性,但不能降低MDA含量。饲料中添加Vc、酵母多糖和壳聚糖均对草鱼的非特异性免疫功能具有一定的促进作用。  相似文献   

酵母细胞壁多糖与铝硅酸盐复合物对猪生长性能、免疫指标及养分消化率的影响     

张勇  郑丽莉  朱宇旌  季文彦  邵彩梅 《动物营养学报》2012,(9):1799-1804

本研究旨在探讨酵母细胞壁多糖(yeast polysaccharide,YP)与铝硅酸盐复合物(alumi-nosilicate complex,AC)对猪的生长性能、免疫指标及养分消化率的影响。试验选用平均体重为(66.18±1.26)kg的"杜×长×大"三元杂交猪140头,随机分成5组,每组4个重复,每个重复7头猪。各组分别饲喂添加不同剂量复合物的试验饲粮,A组为对照组,不添加复合物;B组添加0.1%YP;C组添加0.1%YP和0.9%AC;D组添加0.1%YP和1.9%AC;E组添加0.1%YP和2.9%AC。试验期51 d。结果表明:1)D、E组平均日增重显著低于对照组(P<0.05),各组平均日采食量和料重比差异不显著(P>0.05);2)与对照组相比,D组血清谷胱甘肽过氧化物酶(GSH-Px)活性及补体3(C3)、免疫球蛋白M(IgM)、免疫球蛋白A(IgA)、免疫球蛋白G(IgG)水平显著提高(P<0.05),血清超氧化物歧化酶(SOD)活性和补体4(C4)水平无显著差异(P>0.05);3)各组养分消化率无显著差异(P>0.05)。由此可见,YP和AC复合使用降低了育肥猪的生长性能,0.1%YP和1.9%AC同时添加可增强生长猪的免疫功能。  相似文献   

Interaction of NR2D subunit of NMDA receptor with MOCA     

BAI Ning  YI Fei  LIU Ting  LI Xiao-man 《园艺学报》2016,32(6):1118-1121

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.  相似文献   

酵母壁多糖对断奶仔猪肠道挥发性脂肪酸和微生物菌群的影响     

贺琴  王自蕊  游金明  陈丽玲  熊昊 《动物营养学报》2017,29(1)

本研究旨在探讨饲粮中添加酵母壁多糖对断奶仔猪肠道挥发性脂肪酸和微生物菌群的影响。试验采用单因素试验设计方法,选取180头遗传背景一致、健康状况良好、胎次和体重接近的21日龄断奶仔猪,随机分为4个组,每组5个重复,每个重复9头猪。4个组试验猪分别饲喂对照饲粮(未添加酵母壁多糖)、0.15%酵母壁多糖饲粮、0.30%酵母壁多糖饲粮和0.45%酵母壁多糖饲粮。试验期21 d。结果表明:1)与对照组相比,饲粮中添加0.15%、0.30%和0.45%酵母壁多糖显著提高了仔猪结肠乙酸的含量(P0.05);其中,0.30%和0.45%酵母壁多糖还显著提高了结肠丙酸、丁酸以及总挥发性脂肪酸的含量(P0.05),且二者之间差异不显著(P0.05)。2)与对照组相比,饲粮中添加0.15%、0.30%和0.45%酵母壁多糖显著降低了盲肠沙门氏菌和大肠杆菌数量(P0.05),且0.30%和0.45%酵母壁多糖组之间差异不显著(P0.05)。由此可知,酵母壁多糖可提高仔猪肠道挥发性脂肪酸含量,并改善肠道微生物菌群结构,根据回归方程预测,酵母壁多糖在仔猪饲粮中的适宜添加水平为0.31%~0.40%。  相似文献   

Screening and Analysis of Proteins Interacting with TaPDK from Physiological Male Sterility Induced by CHA in Wheat   总被引：1，自引：0，他引：1  

ZHANG Long-yu  ZHANG Gai-sheng  ZHAO Xin-liang  YANG Shu-ling 《中国农业科学(英文版)》2013,(6):941-950

To further research the regulatory network of pyruvate dehydrogenase kinase (designated as TaPDK) in physiological male-sterility (PHYMS) of wheat induced by chemical hybridizing agent (CHA) SQ-1, an anther cDNA library was constructed, and the proteins interacting with TaPDK were screened via yeast two-hybrid technique. Subsequently, a few candidate proteins in nucleotide expression levels were detected by real-time quantitative PCR. Yeast-two hybrid screening was performed by mating yeast strain Y2HGold containing BD-TaPDK bait plasmid with yeast strain Y187 including anther cDNA library plasmid. Diploid yeast cells were plated on synthetic dropout nutrient medium (SD/-Ade/-His/-Leu/-Trp) (QDO), and further were incubated on QDO medium containing AbA and X-α-Gal. The interactions between TaPDK and the proteins obtained from positive colonies were further confirmed by co-transformation validation. After plasmids DNA were extracted from blue colonies and sequenced, the sequences results were analyzed by bioinformatic methods. Finally, 24 colonies were obtained, including eight genes, namely non-specific lipid-transfer protein precursor (TanLTP), polyubiquitin (TaPUbi), glyceraldehyde-3-phosphate dehydrogenase, proliferating cell nuclear antigen (TaPCNA), CBS domain containing protein (TaCBS), actin, guanine nucleotide-binding protein beta subunit, chalcone synthase, and three new genes with unknown function. The results of quantitative RT-PCR showed that the expression levels of TanLTP, TaPUbi, and TaPCNA were obviously up-regulated in PHYMS anther, and TaCBS expression was only increased at the tricellular stage in PHYMS anther compared with in fertile lines. Whereas, the expression of TaPDK was obviously down-regulated in PHYMS lines. Collectively, these datas indicated that the majority of candidate proteins might be related to pollen abortion in PHYMS lines, which further suggested that TaPDK plays multiple roles in pollen development, besides participating in regulating pyruvate dehydrogenase complex activity.  相似文献