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1.
重组大肠杆菌的高密度发酵和甘油生产条件的初步研究   总被引:2,自引:0,他引:2  
在摇瓶中进行重组大肠杆菌菌株BL21高密度发酵条件的研究,考察了葡萄糖浓度、盐离子浓度、温度、接种量、发酵时间等对该菌株生产甘油的影响。初步确定底物浓度为2.5%,盐离子浓度0.2%,温度为37℃,接种量为2%,经24h的摇瓶发酵,甘油产量最高达6.8g/L。在30L发酵罐实验中、按初步确定的优化条件发酵26h,甘油产量可达46.67g/L,是LB/葡萄糖培养基中甘油产量的2.06倍。  相似文献   

2.
丁酸梭杆菌发酵甘油制备1,3-丙二醇的研究   总被引:3,自引:0,他引:3  
本研究采用丁酸梭芽孢杆菌(Clostridium butyricum)从甘油发酵制备1,3—丙二醇。该发酵需厌氧培养,发酵培养基为:甘油6%,葡萄糖1%,玉米浆2%,(NH4)2SO40.2%。发酵温度为34℃,pH为6.5~7。在最佳条件下,发酵50h可产1,3—丙二醇40.7g/L,甘油摩尔转化率达68%。  相似文献   

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重组毕赤酵母高密度发酵生产内切型纤维素酶的条件优化   总被引:1,自引:0,他引:1  
为优化内切型纤维素酶高密度发酵工艺条件,在7.5L发酵罐高密度发酵条件下,研究内切型纤维素酶表达量以及毕赤酵母胞外蛋白酶合成水平的影响因素。研究表明:经340mL甘油补料发酵后,在甲醇诱导阶段,pH为5.0,温度为25℃,利用甲醇检测流加控制器控制甲醇体积分数为0.33%~0.35%时,EGI表达量可达421.1IU/mL,比采用固定甲醇流加速率的发酵方法提高了1.49倍。  相似文献   

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通过碳源、氮源的单因子实验和正交实验,确定了吸水链霉菌NND-52-C菌株产阿扎霉素B最佳的液体发酵培养基组分(%,质量分数)甘油4.5,玉米粉3,黄豆粉1,蛋白胨1,NaNO30.5,NaCl 0.2,CaCO3 0.3,MgSO4·7H2 O0.05,FeSO4 0.05,PH 7.5;阿扎霉素B最佳的发酵条件发酵前期温度30℃,起始pH 7.5;发酵后期温度28℃,pH6.8;接种量10%,装液量30 mL/250mL摇瓶,发酵时间5 d,最终阿扎霉素B的产量达到l 434 mg/L,比原配方以及原发酵条件提高了76%.  相似文献   

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用不同浓度的甘油包埋绿豆(Phczeolus rodiatus L.)超氧化物岐化酶(Superoxide dismutase,SOD),对不同条件下制备的甘油SOD的稳定性进行评估.结果表明:甘油包埋绿豆SOD的稳定性受甘油浓度影响明显,12.5%~25%为最适甘油浓度.在10℃、pH 6.8、搅拌速度1000 r min-1.条件下包埋的甘油SOD在55℃的平均半衰期为25.1 d,为非包埋SOD的5.1倍.甘油浓度为25%,温度分别为5℃、10℃、25℃、45℃条件下,pH 3.8中包埋的绿豆SOD耐酸性较好,pH 8.9下包埋的绿豆SOD的抗碱能力较强.在包埋过程中添加一定浓度的Zn2 、Cu2 、Fe2 有利于其热稳定性的提高.甘油包埋SOD对一些常见的化妆品添加剂也有一定的抗性.由此可见,甘油包埋技术可望作为一项有应用前景的SOD活性保持新技术,有利于极端温度和极端pH条件下的SOD的应用.  相似文献   

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在3.7 L发酵罐中考察了不同温度23℃~33℃对洋葱伯克霍尔德菌CF-66发酵产抗菌物质CF66I的影响,并对不同温度下的发酵过程进行了动力学特性分析。在此基础之上,提出抗菌物质CF66I合成的分阶段控制策略:发酵过程0~20 h控制温度在30℃,20 h后温度控制在25℃至发酵结束。采用此温度控制策略进行了CF66I的发酵,CF66I的活性达到了3.783 u/mL,比采用单一温度下的最大值提高了26.1%。  相似文献   

7.
本文考察不了同温度(10℃~30℃)对硅藻(Nitzschia laevis)合成二十碳五烯酸(EPA)的影响,对不同温度下的发酵过程进行动力学特性分析。在此基础上,提出了EPA合成的变温培养方法:延滞期及对数期初期温度控制在25℃,从对数期中期开始在20℃条件下进行培养。采用此变温培养进行发酵,EPA的含量和产量分别达到了6.00%和291.60 mg·L-1,较采用单一温度(25℃)发酵的最大值分别提高了24.07%和18.81%。  相似文献   

8.
以玉米粉和木薯淀粉为原料 ,比较了二者的液化和糖化 ,结果表明 :在相同条件下 ,木薯淀粉液化时间较短 ,玉米粉液化时间较长 ,但二者的液化液均较易糖化。然后分别以玉米粉和木薯淀粉糖化液为原料 ,用耐高渗酵母发酵生产甘油 ,研究了玉米浆对二者甘油发酵的影响并对二者进行了比较 ,结果表明 :当玉米粉和木薯淀粉糖化液还原糖含量分别为 2 5 % ,尿素为 0 .2 % ,pH为 4 .5时 ,用玉米粉糖化液发酵甘油时可不添加玉米浆 ,甘油产量最高可达 2 % ,而用木薯淀粉糖化液发酵甘油时 ,适宜的玉米浆为 0 .15 % ,甘油产量最高可达 4 .9%。对二者的比较结果表明 :用玉米粉糖化液为发酵原料时 ,发酵时间较短 ,残糖降低较快 ,甘油产量较低 ,在 36h之后 ,甘油开始反耗。而用木薯淀粉糖化液发酵时 ,发酵时间较长 ,残糖降低较慢 ,甘油产量较高 ,在 72h之后 ,甘油开始反耗。  相似文献   

9.
利用温度调节实现新型重组菌高效转化甘油为D-乳酸   总被引:1,自引:0,他引:1  
油脂水解来源的甘油将是未来发酵工业主要原料之一.文中探索D-乳酸高产大肠杆菌Escherichia coli CICIM B0013-070菌株不同培养温度下好氧与厌氧代谢甘油的特征后,建立并优化了一种新型D-乳酸变温发酵工艺,甘油到乳酸的得率由64%提高到82.6%.另外,在B0013-070中引入了温度诱导型乳酸脱氢酶的转录系统,甘油到乳酸的得率进一步提高到88.9%.  相似文献   

10.
将表达酿酒酵母3-磷酸甘油脱氢酶基因(GPD1)和3-磷酸甘油酯酶基因(HOR2)的质粒PSE-gpd1-hor2转化到甘油激酶基因(glpK)和甘油脱氢酶基因(gldA)双缺失的大肠杆菌JM109C中,构建产甘油的工程菌JM109C/PSE-gpd1-hor2.接种JM109C/pSE-gpd1-hor2和Klebsiella在含1%葡萄糖的摇瓶发酵培养基中37℃发酵56 h,1,3-丙二醇的最高产量为1.28 g/L,葡萄糖摩尔转化率为37.5%;在30 L发酵罐中发酵68 h,1,3-丙二醇的最高产量为24.09 g/L,葡萄糖摩尔转化率为38.0%;5 g/L的乙酸、乳酸,10 g/L的乙醇分别使1,3-丙二醇的产量降低了91.41%、54.68%和51.56%.  相似文献   

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It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.  相似文献   

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Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.  相似文献   

18.
Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.  相似文献   

19.
肝癌中HBV和HCV基因和抗原的分布及意义   总被引:1,自引:0,他引:1  
采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细  相似文献   

20.
For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.  相似文献   

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