响应面法优化沙棘再制奶酪加工工艺

本试验以新鲜沙棘果及奶酪为主要原料,探讨了沙棘再制奶酪的加工工艺。首先经护色、打浆、精磨、过滤、调酸、均质等工序,制备澄清均一的沙棘果汁。以样品感官品质和Vc含量为评价指标,通过单因素试验以及响应面试验,得出最佳配方及工艺为：35.00%天然奶酪、18.56%沙棘果汁（料水质量比1∶1）、1.54%复合乳化盐（m_柠檬酸钠∶m_{多聚磷酸钠}∶m_焦磷酸钠∶m_{六偏磷酸钠}=4∶2∶2∶1）、12.00%黄油、6.00%脱脂乳粉、6.00%白砂糖、0.50%复合稳定剂（m_卡拉胶∶m_黄原胶=4∶1）,其余20.40%为纯净水,乳化温度为84 ℃,乳化时间为11.4 min,搅拌速度为3 000 r/min。经此工艺制成的成品,感官评分为57.5分（满分60分）,Vc含量达16.61 mg/100 g。成品组织结构细腻光滑、色泽橘黄、口感润滑、营养丰富,具有沙棘果的风味,符合《GB25192—2010 再制奶酪》要求。     

杂交构树叶多酚提取工艺优化及其抗氧化活性研究

为建立和优化杂交构树叶多酚的提取工艺,本试验采用超声波辅助提取的方法,以构树叶多酚得率为考察指标,通过单因素试验研究液料比、乙醇浓度、超声时间、超声温度4个因素对构树叶多酚得率的影响;在单因素试验的基础上,借助响应面法设计4因素3水平的试验方案,对构树叶多酚提取的工艺参数进行优化,建立回归模型并进行响应面分析,最终确定最佳的提取工艺参数,并进行3次平行验证;以维生素C为对照,通过测定构树叶多酚对DPPH和ABTS自由基的清除率,评价构树叶多酚的体外抗氧化活性。结果显示：4个因素对构树叶多酚得率的影响顺序依次为：乙醇浓度（B） > 液料比（A） > 超声温度（D） > 超声时间（C）,响应面分析结果显示：两两因素之间存在交互作用,但交互作用不显著（P>0.05）;在液料比为70：1、乙醇浓度为60%、超声时间为50 min、超声温度50 ℃的条件下,构树叶多酚的得率最大,为13.62 mg/g,与响应面法的预测值接近;体外抗氧化试验结果表明,构树叶多酚可以清除DPPH和ABTS自由基,并且在高浓度情况下可以达到与维生素C相当的水平。综上,试验建立的构树叶多酚提取工艺准确、可行,同时证明构树叶多酚具有良好的抗氧化活性;该结果可为构树叶多酚的生物活性研究以及构树叶的药用价值开发提供参考。     

灰铸铁生产技术的一些新进展

对灰铸铁的研究现状和生产中的一些新技术做了评述。重点介绍了高强度薄壁灰铸铁的生产现状以及先进的制造工艺和先进的制造手段在灰铸铁生产中应用所取得的技术成果。     

高效节水灌溉管道流量计算原则初探

对于管网优化及投资分析来说,最不利情况下的水力条件不是普遍条件,不能够完全代表管网应当有的优化假定条件。通过管道控制灌溉面积来确定管道的流量,按照满足在一天内,管道控制的所有灌水器都灌溉一次的原则确定,并给出公式。让管道的流量这一重要参数,在高效节水灌溉工程优化和设计计算中变得简单并容易计算。     

水头可调薄壁堰式渠道流量智能测控系统优化试验研究

采用巴赞堰流公式计算流量的水头可调薄壁堰式渠道流量智能测控系统通过渠道流量量测与控制试验,验证了其精准的测流功能和智能控制技术的可行性。为进一步提高该测控系统运行的效率和稳定性,减少运行能耗,对矩形薄壁堰堰流公式进行水力试验研究,通过分析堰上水头和流量关系,拟合出矩形薄壁堰流量计算公式。通过向该拟合公式引入修正系数λ=0.848,将测控系统测得的堰上水头数据值代入该拟合公式求得的流量值与电磁流量计测得流量值的差值的平均值为-0.004L/s,标准差为0.119,线性相关系数R2=0.989 1。该拟合公式相对于巴赞堰流公式形式简单、参数较少、运算简便,同时也满足节水灌溉对精准测流的要求,更适用于水头可调薄壁堰式渠道流量智能测控系统,对于在灌区推广和使用该测控系统具有重要的意义。     

The Fluorescent Characterization and Analysis of Two Brucella Attenuated Vaccine Infecting Mouse Macrophagocyte

The experiment was conducted to discuss the difference of binding time of green fluorescent protein B.melitensis M5 (GFP-M5) and B.abortus S19 (GFP-S19) infecting the mouse macrophagocyte (RAW264.7),lysosome,endoplasmic reticulum and golgi body in the initial stage and compare the binding rate of GFP-M5,GFP-S19 with organelle in different timeline,respectively,by confocal laser scanning microscope (CLSM) and flow cytometry.The result showed that GFP-M5 and GFP-S19 were successfully constructed.The intracellular survival ability of Brucella M5,Brucella S19,GFP-M5 and GFP-S19 were not obvisouly affected after infecting RAW264.7.GFP-M5 and GFP-S19 could enter the macrophagocyte in 30 mins,and in 2 h the Brucella could reach lysosome,endoplasmic reticulum and golgi body.In addition,the binding time for two attenuated vaccine did not show differences in 1,2,3 and 4 h.The content of GFP⁺ cell produced by RAW264.7 infected by GFP-M5 and GFP-S19 did not show significant differences (P>0.05).Therefore,the two strains did not have significant differences in the invasion ability in the initial stage of infecting host cell.     

Construction and Identification of Yeast Surface Display Libraries of Ovis aries DRA Gene Exon 2

The specific primers were designed according to Ovis aries DRA gene sequence deposited in GenBank and the multiple cloning site of the plasmid pYD1,which was a vector used for protein surface display on Saccharomyces cerevisiae.The gene encoding DRA was amplified by PCR using the genomic RNA of Ovis aries.The 762 bp fragment was cloned and released in GenBank and registration number was KR422362.The PCR product was inserted into the yeast surface display plasmid vector pYD1 by double enzyme digestion.It was indicated that DRA gene was successfully integrated into the genome.Dot mutation was made at both ends of exon 2 in DRA gene for making restriction enzyme cutting site and design the exon 2 specific primers according to mutated Ovis aries DRA gene sequence.Sequenced exon 2 amplification products based on DNA pooling of sheep large sample template was analyzed the polymorphic loci.The polymorphic exon 2 246 bp fragment was obtained by double enzyme digestion and connected to surface display restructuring mutation carriers pYD1-DRA by the same double enzyme digestion,and then we successfully constructed yeast surface display libraries.We transformed it into Saccharomyces cerevisiae EBY100 cell.Yeast monoclone was identified by PCR amplification and sequencing,and we confirmed that DRA gene had been integrated into Saccharomyces cerevisiae genome.After galactose induced,it was detected that DRA gene library had been successfully demonstrated on the yeast cell surface under the fluorescence microscope by immunofluorescence method.     

响应面法优化杜仲叶提取物的制备工艺

优化杜仲叶提取物制备的工艺条件,在单因素试验基础上,以杜仲叶提取物浸膏得率和绿原酸转移率为评价指标,采用Box-Behnken中心组合设计法优化杜仲叶提取物制备的工艺条件。杜仲叶提取物制备的最佳工艺条件为乙醇浓度500mL/L,液料比10∶1(mL/g),提取温度97℃,提取4次,每次30min;在此最佳工艺条件下,杜仲叶提取物浸膏得率和绿原酸转移率综合评分均值为99.08,与预测值基本一致。响应面法(RSM)优化的杜仲叶提取物制备工艺稳定可靠。