lovelymandy
我也在做这个,下面是我整理的,时间关系只能这样了,可以看看。都要求无菌操作 菌种的分离 取lmL卤汁以10倍递增稀释方法(一份酸奶,九份无菌水,再取一份第一只管中溶液,加九份无菌水,依次类推),将其稀释至1/10~10的-10次幂(我打不上去),然后从不同浓度稀 释液中分别取lmL倾注在平皿中,再倒入培养基相混合,待培养基凝固后倒置于30~C恒温下 培养48h。挑取长势良好的单个茵落划线分纯,直至纯化(茵落单个大小一致,革兰氏染色镜 检,茵体一致)。结果分离得到3株不同菌株,分别编号为菌株1、菌株2、菌株3。再分别转移 到试管斜面上进行保存。 分离用培养基:牛肉膏5g,蛋白胨10g,氯化钠5g,蒸馏水1 000 mL,琼脂20g,pH7.0—7.2 ;保存用斜面培养基:酵母膏1% ,碳酸钙2% ,葡萄糖1% ,琼脂2% ,pH 7.0。 培养条件 将分离出的菌株1、菌株2、菌株3分别接种在上述4种不同的培养基上, 在30。【=恒温条件下培养48h后观察并测定其培养结果。 测定方法 菌落总数采用逐级稀释法来计数;pH值用pHS一2C酸度计测定;乳酸定性 及含量测定依据食品检验技术 1I.2.1乳酸菌的分离与筛选的试验程序 自然发酵酸奶---稀释---培养---挑起单菌落染色、镜检一挑 选革兰氏阳性球菌单菌落一Ⅲ号培养基一挑选溶钙圈大的球菌反复在Ⅲ号培养基上几次纯化筛选一单菌落优 良菌株一试管穿刺低温保存。 1.2 1.2 乳酸菌的鉴定 用光学显微镜、放大镜进行乳酸菌的形态特征鉴定。生理生化特征鉴定:产乳 酸定性试验——乳酸纸层析法0- 、过氧化氢酶(接触酶)反应�6�8、明胶水解反应 、硫化氢反应 、乳酸菌 发酵营养型试验0 、耐盐、酸、温度试验。 1.2.I.3 乳酸菌的保存�6�8 采用定期移植低温保藏法。培养基配方:葡萄糖1% 、蛋白胨0 2% 、 l(}l2PQ|0.2%、琼脂20%、pH值7 0,分装试管,121。c灭菌30min。将使用对数生长期后期的细胞进行穿刺 培养,然后密封存于冰箱玲藏室内(5qc左右),2个月移植1次。 1.2.2 分离乳酸菌的生理特点试验 1 2 2.1 最适生长温度的测定OD值以同温下不接种培养基作对照,定期取出接种培养基在721分光光度 计上,用最大吸收光波长 =6001RIifl测定。 1.2.2.2 生长周期的测定oD值(方法同上);pH值:PHB一4pH计;可滴定酸(以乳酸计):吸取ImL菌液 加入9Ⅱ1L蒸馏水,加入1~2滴酚酞,用0.1NNaOH滴定。 1.2 2.3 最适pH值的测试、最适盐浓度的测试。 供试样品及培养基 分离用样品:酸奶、酸奶及西红柿均为市售 分离用培养基:①BCP培养基:酵母膏2 5g,蛋白胨5g,葡萄糖5g,溴甲酚紫0 04g,琼脂15g, 蒸槽水lO00ml,pH7 0;②MRS培养基见文献 。 菌种保藏用培养基:脱脂乳培养基:新鲜牛乳离心去掉上层乳脂,下层奶液分装试管,105℃ 灭菌20mln。 菌利 鉴定用培养基见文献 6。 1 2 方法 1 2 1 乳酸菌的分离纯化 取泡菜汁、酸奶、西红柿表面洗液进行梯度稀释,分别用倾注法、涂布 法和划线法在BCP和MRS培养基平板上进行菌种分离。挑取在BCP平板上有透明目的菌落,在 MRS平扳上有溶钙圈的菌落,反复纯化至纯种,挑菌至脱脂牛奶试管中保存 1.2 2 乳酸菌复筛对初筛菌株进行革兰氏染色,保留革兰氏阳性菌株.并对其所产乳酸能力进 行定性、定量分析,筛选出产酸高的菌株保存,再把产酸高的菌株经萝l、汁发酵 】,进一步选择产 酸高、_l】味纯正的菌株保存鉴定 1 2 3 乳酸定性测定果用纸层析法。溶剂系统为乙醇:浓氨水:水=80:5:15,显色剂为0 04% 的溴甲酚紫酒精溶液。层析时将乳酸、柠檬酸配成1% 的标准溶液,两种标准溶液 及乳酸发酵液 均点样3 .上行层析,显色与标准样比较 1.2 4 乳酸的定量测定采用气相色谱法,利用苄酯化法制备乳酸衍生物,将待测乳酸菌株在产 酸培养基内37"C培养3d,离心。取上清液剃备衍生物,气相色谱分析含量。气相色谱工作条件为: EGS色谱柱,柱温160'C,气化温度180'17.,检测器温度l70"C,载气为N,。 1.2 5 菌种鉴定根据《简明第八版伯杰细菌鉴定手册》 和《一般细菌常用鉴定手册》[6 对复筛 出的菌株的形态、生理生化、碳源利用等方面进行系统鉴定,并提取乳酸菌株DNA,采用熔链温度
面包超人311
国际会议特邀报告:1. 2009年8月,第7届中日韩反刍动物瘤胃生理与调控学术研讨会Keynote speech,韩国,首尔。2. 2008年9月,第13届亚澳动物科学代表大会 (13th AAAP Animal Science Congress)作动物营养专题报告(invited paper),越南,河内。3. 2007年9月,第七届国际草食动物营养研讨会,大会特邀报告(plenary paper),北京;发表的主要论文 (* 为通讯作者)1) Dai ZL, Zhang J, Wu G, Zhu W-Y*, 2010. Utilization of amino acids by bacteria from the pig small intestine. Amino Acids, 39 (5): 1201-1215.2) Huang RH, Qiu XS, Shi FX, Hughes CL, Lu ZF, Zhu W Y*. 2010. Effects of dietary allicin on health and growth performance of weanling piglets and reduction in attractiveness of faeces to flies. Animal, (first view)3) Pei CX, Mao SY, Cheng YF, Zhu W-Y*, 2010. Diversity, abundance and novel 16S rRNA gene sequences of methanogens in rumen liquid, solid and epithelium fractions of Jinnan cattle. Animal, 4(1):20–294) Sun YZ, Mao SY, Zhu W-Y*. 2010. Rumen chemical and bacterial changes during stepwise adaptation to a high concentrate diet in goats. Animal, 4(2):210–2175) Cheng Y F, Edwards J E., Allison G G., Zhu W-Y* and Theodorou M K., 2009. Diversity and activity of enriched ruminal cultures of anaerobic fungi and methanogens grown together in consecutive batch culture. Bioresource Technology, 100 (2009) 4821–4828.6) Lu Y, Sarson AJ, Gong J, Zhou H, Zhu W-Y, Kang Z, Yu H, Sharif S, Han Y. Expression profiles of genes in Toll-like receptor-mediated signaling of broilers infected with Clostridium perfringens. Clinical and Vaccine Immunology, 2009, 16(11):1639-1647.7) Iqbal MF, Zhu W-Y*, 2009. Characterization of newly isolated Lactobacillus delbrueckii –like strain MF-07 isolated from chicken and its role in isoflavone biotransformation. FEMS Microbiology Letters, 291 (2): 180-187, FEB 20098) Iqbal MF, Zhu W-Y*, 2009. Bioactivation of flavonoid diglycosides by chicken cecal bacteria. FEMS Microbiology Letters, 2009, 295, 30-41.9) Cheng YF, Mao SY, Liu JX, Zhu WY*, 2009. Molecular diversity analysis of rumen methanogenic Archaea from goat in eastern China by DGGE methods using different primer pairs. Letters in Applied Microbiology, 2009, 48(5):585-592.10) Zhou, W, Wang, GJ, Han, ZK, Yao, W, Zhu, WY. 2009. Metabolism of flaxseed lignans in the rumen and its impact on ruminal metabolism and flora. Animal Feed Science and Technology, 150 (1-2): 18-26.11) Zhou, W, Han, ZK, Zhu, WY, 2009. The metabolism of linseed lignans in rumen and its impact on ruminal metabolism in male goats. Journal of Animal and Feed Science, 18 (1): 51-60 200912) Su Y, Yao W, Perez O, Smidt H, Zhu W-Y*, 2008. Changes in abundance of Lactobacillus spp. and Streptococcus suis in stomach, jejunum and ileum of piglets after weaning. FEMS Microbiology Ecology, 66:546-555.13) Yu ZT, Yao W, Zhu WY*, 2008. Isolation and identification of equol-producing bacterial strains from cultures of pig faeces. FEMS Microbiol Lett 2008, 282:73–80.14) Su Y, Yao W, Perez-Gutierrez ON, Smidt H, Zhu WY*.2008. 16S ribosomal RNA-based methods to monitor changes in the hindgut bacterial community of piglets after oral administration of Lactobacillus sobrius S1. Anaerobe, 14(2): 78-86.15) Mao SY, Zhang G, Zhu WY*, 2008. Effect of disodium fumarate on ruminal metabolism and rumen bacterial communities in goat as revealed by denaturing gradient gel electrophoresis analysis of 16S ribosomal DNA. Animal Feed Science and Technology, 140 (2008) 293–306.16) Mao SY, Zhang G, Zhu WY*, 2008. Effect of disodium fumarate on ruminal metabolism and rumen bacterial communities in goat as revealed by denaturing gradient gel electrophoresis analysis of 16S ribosomal DNA. Animal Feed Science and Technology, 2008, 140: 293–306.17) Iqbal MF, Cheng YF, Zhu WY*, Zeshan B, 2008. Mitigation of ruminant methane production: current strategies, constraints and future options. World J Microbiol Biotechnol, 24:2747-2755.18) Sun YZ, Mao SY, Yao W, Zhu WY*. 2008. DGGE and 16S rDNA analysis reveals a highly diverse and rapidly colonising bacterial community on different substrates in the rumen of goats. Animal, 2008, 2 (3): 391–39819) Guo, YQ, Liu, JX, Lu, Y, Zhu, WY, Denman, SE, McSweeney, CS, 2008. Effect of tea saponin on methanogenesis, microbial community structure and expression of mcrA gene, in cultures of rumen micro-organisms. Letters in Applied Microbiology, 47(5):421-426.20) Zhang, CM, Guo, YQ, Yuan, ZP, Wu, YM, Wang, JK, Liu, JX, Zhu, WY. 2008. Effect of octadeca carbon fatty acids on microbial fermentation, methanogenesis and microbial flora in vitro. Animal Feed Science and Technology, 146(3-4):59-269.21) Mao SY, Zhu WY*, Wang QJ, Yao W. 2007, Effect of daidzein on in vitro fermentation of micro-organisms from the goat rumen. Animal Feed Science and Technology, 136:154-163.22) Mao SY, Zhang G, Zhu WY*, 2007, Effect of disodium fumarate on in vitro rumen fermentation of different substrates and rumen bacterial communities as revealed by denaturing gradient gel electrophoresis analysis of 16S ribosomal DNA. Asia-Australian Journal of Animal Sciences, 20 (4): 543-549.23) Liu W, Mao SY, Zhu WY*, 2007. Impact of tiny miRNAs on cancers. World Journal of Gastroenterology, 13(4):497-502.24) Yu QH, Dong SM, Zhu WY, Yang Q, 2007. Use of green fluorescent protein to monitor Lactobacillus in the gastro-intestinal tract of chicken. FEMS Microbiology Letters, 275 (2): 207-213.25) Wang HF, Zhu WY, Yao W, Liu JX, 2007. DGGE and 16S rDNA sequencing analysis of bacterial communities in colon content and feces of pigs fed whole crop rice. Anaerobe 13: 127-133.26) Li MY, Zhou GH, Xu XL, Li CB, Zhu WY. Changes of bacterial diversity and main flora in chilled pork during storage using PCR-DGGE. Food Microbiology, 2006, 23: 601-611.27) Zhu WY*, Mao SY, Liu JX, Cheng YF, Iqbal MF, Wang JK, 2007. Diversity of methanogens and their interactions with other microorganisms in methanogenesis in the rumen. Plenary Paper, Proceedings of the 7th International Symposium on the Nutrition of Herbivores, pp 125-139, Beijing, September 17 – 22, 2007.28) Zhu WY*, Iqbal M F, Cheng YF, Liu JX, Mao SY, 2008. Rumen methanogenesis and nutritional approaches to the mitigation of ruminant methane. Invited paper, The 13th Animal Science Congress of the Asian – Australasian Association of Animal Production Societies, International Symposium: ”Recent Advances in Ruminant Nutrition”, pp 33-40, 2008/9/2229) Zhu WY*, Mao SY, Cheng YF, Liu JX, Wang JK, 2009. Rumen microbial communities involved in methanogenesis and nutritional strategies to mitigate. Invited Keynote Speech: The 7th Korea-Japan-China Joint symposium on Rumen Metabolism and Physiology, 2009/8/5.30) Han ZK, Wang GJ, Yao W, Zhu WY*. 2006. Isoflavonic phytoestrogens - new prebiotics for farm animals: a review on research in China. Current Issues in Intestinal Microbiology, 7:53-60.31) 毛胜勇,王新峰,朱伟云,2010. 体外法研究延胡索酸二钠对瘤胃微生物发酵活力及甲烷产量的影响。草业学报,19(2):69-75。32) 毛胜勇,龙黎明,朱伟云,2010. 体外研究反刍兽新月形单胞菌及与酵母联用对瘤胃微生物发酵的影响。草业学报,19(8):176-186。33) 陆扬,姚文,苏勇,朱伟云*, 2010. 大豆苷元对断奶仔猪胃肠道发育的影响. 南京农业大学学报,33(2):91-95.34) 成艳芬,朱伟云*,2009. ARISA方法研究产甲烷菌共存及去除条件下瘤胃真菌多样性变化。微生物学报,2009, 49(4):504-511.35) 杭苏琴,戴兆来,朱伟云*,2009,甘露寡糖对纯培养和共培养的乳酸杆菌体外生长的影响。微生物学通报,2009,36(1):51-56.36) 于卓腾,姚文,朱伟云*,2009,体外培养发现二花脸猪粪样菌群具有降解大豆黄酮产生雌马酚的能力。南京农业大学学报,2009,32(1):164-167。37) 刘相玉,毛胜勇,朱伟云*,2009,高精料日粮条件下酵母培养物对瘤胃细菌体外发酵的影响。动物营养学报,2009,21(2):199-204.38) 龙黎明,毛胜勇,苏勇,朱伟云,一株瘤胃源乳酸利用菌的分离鉴定及其体外代谢特性研究。微生物学报,2008,48(12):1571-1577。39) 苏勇,姚文,朱伟云*,代表性差异分析比较两株来自不同地区的猪源Lactobacillus 菌株。微生物学报,2008,48(5):1~6。40) 戴兆来,董红军,林勇,黄瑞华,朱伟云*,合生元组合筛选及对仔猪生产性能和腹泻的影响。南京农业大学学报,2008,31(2):81-85。41) 裴彩霞, 毛胜勇, 朱伟云*,晋南牛瘤胃中古菌分子多样性的研究。微生物学报,2008,48(1):8-14。42) 俞晓辉,姚文,施学仕,朱伟云,大豆发酵蛋白替代鱼粉对断奶仔猪生产性能和肠道主要菌群的影响。动物营养学报,2008,20(1):46-51。43) 罗玉衡,朱伟云*,2007,消化道微生物区系与肥胖关系的研究进展。微生物学报,47(6):1115-1118。44) 刘威,朱伟云*,姚文,毛胜勇,2007,一株乳酸利用、丁酸产生菌的分离与鉴定及代谢特性的初步研究。微生物学报,47(3):435-440。45) 张耿,朱伟云*,刘相玉,毛胜勇,2007,延胡索酸二钠对瘤胃微生物体外发酵不同饲料成分的影响。草业学报,16:112-117。46) 于卓腾 姚 文 毛胜勇 朱伟云*,2007,黄豆苷元对仔猪肠道微生物区系的影响。营养学报,29(1):82-86。47) 姚光国,姚文,陆扬,朱伟云*,2007,乳酸菌肽聚糖部分免疫增强作用的研究。微生物学通报,34(1):105-107。48) 成艳芬,毛胜勇,裴彩霞,刘建新,朱伟云*,共存于厌氧真菌分离培养液中瘤胃甲烷菌的检测及其多样性分析。微生物学报,2006,46(6):879-883。49) 孙云章,毛胜勇,姚文,朱伟云*,2006,不同精粗比底物下瘤胃真菌和纤维降解细菌共培养发酵特性及菌群变化。微生物学报,46(3):422-426。50) 姚文,朱伟云*, 毛胜勇,2006,16S rDNA技术跟踪分析新生腹泻仔猪粪样细菌区系的变化。微生物学报,45(1):150-154。专利等成果1. 发明专利:一种芽孢乳杆菌及其生产的活菌制剂。(授权公开日:2007年6月20日);2. 国家发明专利受理一项:绞股蓝皂甙用于减少动物瘤胃内甲烷产生的方法。3. 成果鉴定:仔猪肠道微生物区系研究及芽孢乳杆菌S1研制。苏科鉴字【2004】第1308号。鉴定形式:会议鉴定。组织鉴定单位:江苏省科技厅。鉴定日期:2005年1月29日。
耐胆酸盐吧, 可以较好地通过动物肠道, 达到目的地起作用, 耐盐乳酸菌当然也耐酸,耐胃酸等. 有保护处理的乳酸菌更好.
1.形态和培养特征观察 采用牛肉膏蛋白胨培养基,将已纯化后的甘油菌种活化后于37℃下培养20~24h ,并进行革兰氏染色及菌体形态和菌落特征的观察。染色方法参照
这不是正大老师布置的论文作业们 哈哈哈啊哈哈
酸碱中和滴定实质是酸电离出的H+和碱电离出的OH-以等物质的量关系结合成水。酸碱中和滴定中,在滴定到达终点前,溶液PH值随着标准液体积的变化很小,在将要到达终点
茚三酮显色法。 游离氨基酸总量测定常用方法为茚三酮显色法,氨基酸为水溶性物质,在pH为8.0的缓冲溶液中与茚三酮同时加热,可形成紫色络合物,在吸收波长570纳米