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Low-Temperature Response to Major Agronomic Traits by Using Recombinant Inbred Line(RIL) Populations Derived from Towada × Kunmingxiaobaigu 被引量:1
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作者 XU Fu-rong YU Teng-qiong TANG Cui-feng A Xin-xiang FAN Chuan-zhang HU Yi-liang ZHANG Dun-yu DONG Chao DAI Lu-yuan 《Agricultural Sciences in China》 CAS CSCD 2009年第11期1301-1311,共11页
Development of the recombinant inbred line populations (RILs) is important basis to detect QTLs for cold tolerance at booting stage in rice. A set of 230 RILs derived from the cross of Towada and Kunmingxiaobaigu we... Development of the recombinant inbred line populations (RILs) is important basis to detect QTLs for cold tolerance at booting stage in rice. A set of 230 RILs derived from the cross of Towada and Kunmingxiaobaigu were used for evaluation of low-temperature response on major agronomic traits of plant height (PH), panicle length (PL), panicle exsertion (PE), spikelet fertility (SF), specific spikelet fertility (SSF), and spikelets per panicle (SPP) under natural low-temperature growing environments in Yunnan Province, China. The results showed PH, PE, and SPP were mainly attributed by genotypes. PL was mainly influenced interactively by the genotypes × environments. SF and SSF were mainly controlled by the environments. Under the five different growth environments, F values of the six agronomic traits mentioned above ranged from 4.019 to 97.284. Significant difference was revealed between the lines. Under every environment, it indicated significantly positive correlation between SF and SSF, with correlation coefficients ranged from 0.826 to 0.885. It indicated significantly positive correlation between PH, PL, and PE. Under five different growing environments, variation coefficients of the six characters ordered in SSF (66.3%) 〉 PE (57.4%) 〉 SP (37.2%) 〉 SPP (16.2%) 〉 PH (9.6%) 〉 PL (6.4%). SSF, PE and SF were most sensitive to low temperature stress at booting stage, while SPP, PH and PL being least. The RILs of Towada/ Kunmingxiaobaigu can be used as a genetic population to investigate cold tolerance at booting stage. SSF, PE and SF are most sensitive to cold tolerance at booting stage in rice. So far the the variation of PH, PL, and SPP related to cold tolerance are not clear under natural low-temperature environment. More tested environments and years are required to identify and evaluate cold tolerance at booting stage in rice. 展开更多
关键词 ANOVA correlation analysis low-temperature response major agronomic traits recombination inbred line population (RIL) Oryza sativa L. sp. japonica
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温度对铜绿微囊藻(Microcystis aeruginosa)和鱼腥藻(Anabaena sp.)生长及胞外有机物产生的影响 被引量:14
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作者 刘菲菲 冯慕华 +2 位作者 尚丽霞 何延召 李文朝 《湖泊科学》 EI CAS CSCD 北大核心 2014年第5期780-788,共9页
以巢湖优势种铜绿微囊藻(Microcystis aeruginosa)和鱼腥藻(Anabaena sp.)为研究对象,研究不同温度(35、25和10℃)对这两种藻生长特性和胞外有机物产生的影响.结果表明,温度对铜绿微囊藻和鱼腥藻的藻细胞密度、碱性磷酸酶活性和胞外有... 以巢湖优势种铜绿微囊藻(Microcystis aeruginosa)和鱼腥藻(Anabaena sp.)为研究对象,研究不同温度(35、25和10℃)对这两种藻生长特性和胞外有机物产生的影响.结果表明,温度对铜绿微囊藻和鱼腥藻的藻细胞密度、碱性磷酸酶活性和胞外有机物浓度影响显著.25℃是铜绿微囊藻和鱼腥藻最适宜的生长温度,最高细胞密度分别达到3.12×107cells/ml和2.03×107cells/ml.不同温度下两种藻的碱性磷酸酶活性特征,证实了高温对鱼腥藻生长的抑制和低温对铜绿微囊藻生长的抑制.胞外有机物释放总量受蓝藻生物量和单位细胞有机物释放速率的影响.铜绿微囊藻的溶解性有机碳和胞外总多糖释放量在25℃最高,最大值分别为49.28和38.46 mg/L;而鱼腥藻在35℃时释放量最高,最大值分别为45.82和40.60 mg/L;10℃条件抑制了两种藻的生长及胞外有机物的释放.鱼腥藻胞外多糖含量在35℃培养条件下最高,而铜绿微囊藻在10℃条件下最高,说明不利的生长条件会促进蓝藻胞外多糖的分泌.三维荧光图谱分析结果表明,铜绿微囊藻和鱼腥藻胞外有机物以类蛋白质和类腐殖酸为主,温度主要影响藻细胞胞外有机物浓度,而对有机物种类组成没有影响. 展开更多
关键词 铜绿微囊藻 鱼腥藻 碱性磷酸酶活性 胞外多糖 温度 巢湖 anabaena sp.
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碳氮源对转基因鱼腥藻Anabaena sp.PCC7120培养的影响 被引量:6
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作者 刘志伟 郭勇 张晨 《工业微生物》 CAS CSCD 北大核心 2001年第2期23-25,共3页
对碳源、氮源种类和用量对转rhTNF -α基因鱼腥藻 712 0 (Anabaenasp .PCC712 0 )培养的影响进行了研究 ,发现最适碳源为蔗糖 ,最适氮源为NaNO3 ,最佳用量分别为 9g/L和 2 .2 5g/L ,此时生物量远高于自养方式 ,达 2 .5 2 g/L ,比相同条... 对碳源、氮源种类和用量对转rhTNF -α基因鱼腥藻 712 0 (Anabaenasp .PCC712 0 )培养的影响进行了研究 ,发现最适碳源为蔗糖 ,最适氮源为NaNO3 ,最佳用量分别为 9g/L和 2 .2 5g/L ,此时生物量远高于自养方式 ,达 2 .5 2 g/L ,比相同条件下在BG - 11培养基培养高 71.66%,TNF-α表达量为 16%~ 2 2 %,生物活性为 10 5U /mg。 展开更多
关键词 碳源 氮源 转基因鱼腹藻 肿瘤坏死因子 培养
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鱼腥藻Anabaena sp.PCC7120的混合营养生长 被引量:7
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作者 喻国策 辛晓峰 +2 位作者 蔡昭铃 施定基 欧阳藩 《化工冶金》 EI CSCD 北大核心 2000年第1期52-57,共6页
在高光强为160μE/(m2·s)、低光强为16μE/(m2·s)、葡萄糖浓度0~30g/L范围内,、进行了鱼腥藻Anabaenasp.PCC7120的摇瓶光自养和混合营养培养.在高光强下最大藻细胞密度(0.... 在高光强为160μE/(m2·s)、低光强为16μE/(m2·s)、葡萄糖浓度0~30g/L范围内,、进行了鱼腥藻Anabaenasp.PCC7120的摇瓶光自养和混合营养培养.在高光强下最大藻细胞密度(0.92~3.1g/L)明显高于低光强(0.11~0.58g/L),而且高光强使混合营养培养的对数期缩短.在不同光强下,葡萄糖浓度在0~18g/L范围内提高显著促进了细胞的生长,在18~30g/L范围内变化对细胞生长不再有更大的影响.高光强促进了藻细胞对葡萄糖的利用.在高光强下随着葡萄糖浓度的提高,细胞得率逐渐变小. 展开更多
关键词 鱼腥藻 混合营养培养 光强 葡萄糖消耗
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维生素对转基因鱼腥藻Anabaena sp.PCC7120培养的影响 被引量:5
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作者 刘志伟 张晨 郭勇 《水生生物学报》 CAS CSCD 北大核心 2002年第6期722-724,共3页
关键词 维生素 转基因鱼腥藻 藻类培养 生长因子
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无机盐诱导鱼腥藻595(Anabaena sp.595)的细胞学效应 被引量:3
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作者 吴红艳 赵以军 +2 位作者 郭厚良 张婷 吴涛 《植物学通报》 CSCD 北大核心 2003年第2期205-211,共7页
鱼腥藻 5 95 (Anabaenasp .5 95 )在 0 .0 5mol/L钾、钠、铵的盐酸盐、硝酸盐、硫酸盐和磷酸盐的诱导下 ,2d后即出现显著的细胞学效应 :细胞体积增大 ,明显液泡化 ;少数细胞发生横向和不均等分裂 ;藻丝片段化 ,异形胞分化率相对提高。其... 鱼腥藻 5 95 (Anabaenasp .5 95 )在 0 .0 5mol/L钾、钠、铵的盐酸盐、硝酸盐、硫酸盐和磷酸盐的诱导下 ,2d后即出现显著的细胞学效应 :细胞体积增大 ,明显液泡化 ;少数细胞发生横向和不均等分裂 ;藻丝片段化 ,异形胞分化率相对提高。其中 ,铵盐培养的藻丝细胞内出现特异的浓缩颗粒状区域。钙盐、镁盐也诱导类似细胞学变化 ,但作用较弱。在含 0 .1mol/LNaCl的培养基中长期培养 ,细胞出现周期性分化行为 ,开始细胞膨大并液泡化 ,以后色素质重新充满细胞 ,液泡消失 ,然后细胞分裂至正常细胞大小 ,成为接近正常的藻丝 ,但接着又膨大液泡化 。 展开更多
关键词 鱼腥藻595 细胞学效应 无机盐 盐胁迫 藻丝片段化 异形胞分化率 液泡化 周期性分化行为
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蓝藻Anabaena sp.PCC7120羧体碳酸酐酶的鉴定 被引量:1
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作者 吴天福 宋立荣 刘永定 《水生生物学报》 CAS CSCD 北大核心 1999年第5期409-413,共5页
在丝状蓝藻AnabaenaspPCC7120细胞租提液的碳酸酥酶(CA)分析中,发现了两种形式的CA活性.高CO2下生长的细胞,在35pmol/LEZ(Ethoxyzoamide,碳酸醉酶的抑制剂)存在的情况下,CA总活性的85%左右被抑制,其半抑制浓度I50为7.4μmol... 在丝状蓝藻AnabaenaspPCC7120细胞租提液的碳酸酥酶(CA)分析中,发现了两种形式的CA活性.高CO2下生长的细胞,在35pmol/LEZ(Ethoxyzoamide,碳酸醉酶的抑制剂)存在的情况下,CA总活性的85%左右被抑制,其半抑制浓度I50为7.4μmol/L;随着EZ浓度的继续增加,CA活性在EZ浓度达到约150μmol/L处出现了第二个抑制峰,在250μmol/L处抑制程度达到最大,使CA总活性的15%被抑制,其半抑制浓度I50为190μmol/L.在空气条件下生长的细胞中也出现了CA的两个抑制峰:低I50为6μmol/L,高I50为120μmol/L.对核体的分离及体外测试表明,在波体制备物中的CA活性只有一个EZ的抑制峰,而且在EZ浓度达到35μmol/L,正如所期望的那样,该CA活性全部被抑制.其半抑制浓度150为5.2μmol/L左右.这个值跟空气或高CO2条件下生长的细胞粗提物中的低I50(6μmol/L或7.4μmol/L)十分相似.说明低浓度的EZ可以特异性地抑制定位于校体的CA活性.另外一种形式的CA,具有高I50(120-190μmol/L),约占CA总活性的15-20%,则有可能定位于细胞质膜. 展开更多
关键词 蓝藻 anabaenasp.PCC7120 羧体碳酸酐酶
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Influences of Nitrogen-phosphorus Ratio on the Growth and Competition of Chlorella vulga and Anabaena sp. strain PCC
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作者 王菁 裘丽萍 +3 位作者 孟顺龙 范立民 宋超 陈家长 《Agricultural Science & Technology》 CAS 2015年第8期1757-1762,共6页
This paper studied the effects of different ratios of nitrogen and phospho- rus on the growth and competition of Anabaena sp. strain PCC and chloralla vul- gads (low nitrogen-phosphorus ratio group: N/P=16:1; Mediu... This paper studied the effects of different ratios of nitrogen and phospho- rus on the growth and competition of Anabaena sp. strain PCC and chloralla vul- gads (low nitrogen-phosphorus ratio group: N/P=16:1; Medium low nitrogen-phospho- rus ratio group: N/P=32:1; Medium high nitrogen-phosphorus ratio group: N/P=64:1; High nitrogen-phosphorus ratio group: N/P=320:1). Results suggested that the largest amount of anabaena sp.strain PCC survived in medium high nitrogen-phosphorus ratio group. The nitrogen-phosphorus ratio showed no significant influences on the growth of Chlorella vulgaris, but it exerted dramatic influences on the growth of Chlore/la vulgaris of the mixed cultivation system. The largest amount of Ch/orel/a vulgaris can be found in the medium-high nitrogen-phosphorus ratio group. The inhi- bition parameter of nitrogen-phosphorus on the algae was distinctive. Anabaena sp. strain PCC had advantages in the competition with the low nitrogen-phosphorus ra- tio and medium-low nitrogen-phosphorus ratio. Potential instability existed between anabaena sp.strain PCC and Chlorella vulgaris when the nitrogen to phosphorus ratio was medium-high and high. 展开更多
关键词 anabaena sp. strain PCC Chlorel/a vulgaris The ratio of nitrogen tophosphorus Interspecies competition
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Expression of Mouse MT-1 as a Fusion Protein in Anabaena sp. PCC 7120
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作者 周杰 郝福英 +2 位作者 施定基 俞梅敏 茹炳根 《Acta Botanica Sinica》 CSCD 2003年第1期98-101,共4页
To produce mouse metallothionein-1 (mMT-I ) in cyanobacterium Anabaena sp. PCC 7120, a novel Escherichia co/i-cyanobacterium shuttle fusion expression vector, pKG-MT, was constructed. Via this vector, mMT-I cDNA which... To produce mouse metallothionein-1 (mMT-I ) in cyanobacterium Anabaena sp. PCC 7120, a novel Escherichia co/i-cyanobacterium shuttle fusion expression vector, pKG-MT, was constructed. Via this vector, mMT-I cDNA which was fused with a carboxyl terminal extension of the 26 kD glutathione-S-trans-ferase (GST) containing a thrombin specific site was expressed in Anabaena under the control of tac promoter. SDS-polyacrylamid gel electrophoresis (SDS-PAGE) showed that the fusion protein GST-MT was expressed in the transgenic Anabaena sp. PCC 7120 after induction with isopropylthio-β-D-galactoside (IPTG). Glutatione-S-transferase metallothionein (GST-MT) was purified from the crude extracts by affinity chromatography on immobilized glutathione and mMT- I was obtained by digesting the fusion protein with thrombin on column and gel filtration on Sephadex G-50. SDS-PAGE demonstrated that the purified mMT- I was the desired protein. The result of ELISA for the purified mMT-I showed that the recovery of mMT- I from the transgenic cyanobacterium was about 0.6 mg/g fresh weight. According to the data of atomic absorption assay, metal-binding activity of the purified mMT-I was almost the same as that of wild type MT. 展开更多
关键词 mouse metallothionein-I anabaena sp. PCC 7120 fusion expression affinity chromatography
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Effect of Iron Deficiency on Heterocyst Differentiation and Physiology of the Filamentous Cyanobacterium Anabaena sp. PCC 7120 被引量:1
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作者 XuWen-liang LiuYong-ding ZhangCheng-cai 《Wuhan University Journal of Natural Sciences》 CAS 2003年第03A期880-884,共5页
The effect of iron deficiency on heterocyst differentiation and some physiological properties of the filamentous cyanobacterium Anabaena sp. PCC 7120 was investigated. Under moderate iron limitation conditions, ac... The effect of iron deficiency on heterocyst differentiation and some physiological properties of the filamentous cyanobacterium Anabaena sp. PCC 7120 was investigated. Under moderate iron limitation conditions, achieved by addition of iron chelator 2,2′\|Dipyridyl (<80 μmol/L) led to delayed heterocyst differentiation, no heterocyst differentiation was observed under severe iron limitation conditions, when the concentration of 2,2′\|Dipyridyl in the medium was more than 100 μmol/L . It seemed that there are certain iron\|regulated genes or operons whose function is to control heterocyst development. In addition, iron deficiency impaired the growth. Low\|iron cells had a decrease in the quantities of pigment content (chlorophyll and phycocyanin content),the whole cell in vivo absorbance spectra confirmed the decrease, the protein electrophoretic profiles revealed that iron\|deficient cells had less protein bands, with the increase of 2,2′\|Dipyridyl ,the protein bands was more and more less. And differently, iron deficiency also caused an increase of ROS (Reactive Oxygen Species)and SOD activity, it suggests that iron deficiency led to oxidative stress, which generally occured under high\|iron conditions. 展开更多
关键词 anabaena sp. PCC 7120 iron deficiency heterocyst development protein SDS \|PAGE oxidative stress
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Growth and Physiological Features of Cyanobacterium Anabaena sp. Strain PCC 7120 in a Glucose-Mixotrophic Culture 被引量:1
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作者 喻国策 施定基 +2 位作者 蔡昭铃 丛威 欧阳藩 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2011年第1期108-115,共8页
Mixotrophic growth is one potential mode for mass culture of microalgae and cyanobacteria particularly suitable for the production of high value bioactive compounds and fine chemicals.The typical heterocystous cyanoba... Mixotrophic growth is one potential mode for mass culture of microalgae and cyanobacteria particularly suitable for the production of high value bioactive compounds and fine chemicals.The typical heterocystous cyanobacterium Anabaena sp.PCC 7120 was grown in the presence of exogenous glucose in light.Glucose improved the cell growth evidently,the maximal specific growth rate under mixotrophic condition(0.38 d 1)being 1.6-fold of that of photoautotrophic growth.Mixotrophy caused a variation in cellular pigment composition,increasing the content of chlorophyll a and decreasing the contents of carotenoid and phycobiliprotein relative to chlorophyll a.Fluorescence emission from photosystem II(PSII)relative to photosystem I was enhanced in mixotrophic cells,implying an increased energy distribution in PSII.Glucokinase(EC 2.7.1.2)activity was further induced in the presence of glucose.The mixotrophic culture was scaled up in a 15 L airlift photobioreactor equipped with an inner and an outer light source.A modified Monod model incorporating the specific growth rate and the average light intensity in the reactor was developed to describe cell growth appropriately.The understanding of mixotrophic growth and relevant physiological features of Anabaena sp.PCC 7120 would be meaningful for cultivation and exploitation of this important cyanobacterial strain. 展开更多
关键词 cyanobacteria anabaena sp.PCC 7120 growth features mixotrophic culture PHOTOBIOREACTOR
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Cloning and Characterization of the fecC Gene Necessary for Optimal Growth under Iron-Deficiency Conditions in the Cyanobacterium Anabaena sp. PCC7120
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作者 xuwen-liang LIUYong-ding +1 位作者 ZHANGCheng-cai LIJuan 《Wuhan University Journal of Natural Sciences》 EI CAS 2004年第4期498-502,共5页
ThefecC gene encoding a putative iron (III) dicitrate transporter was cloned from nitrogen-fixing cyanobacteriumAnabaena sp. PCC 7120, and inactivated. The mutant grows normally in medium with NO 3 ? , NH 4 + or witho... ThefecC gene encoding a putative iron (III) dicitrate transporter was cloned from nitrogen-fixing cyanobacteriumAnabaena sp. PCC 7120, and inactivated. The mutant grows normally in medium with NO 3 ? , NH 4 + or without combined nitrogen. But in iron-deficient medium, the mutant grows slowly. Photosynthetic properties were compared between the mutant and the wildtype strain, the content of photosynthetic pigments in the mutant is lower than that of the wild-type. The results of RT-PCR experiments show that thefecC gene is expressed under iron-deficient conditions, but is not expressed under iron-replete conditions. These results revealed thatfecC gene product is required for optimal growth under iron-deficient conditions inAnabaena sp. PCC 7120. Key words Anabaena sp. PCC 7120 - fecC - iron deficiency - photosynthetic properties - expression CLC number Q 933 Foundation item: Supported by the National Natural Sciences Foundation of China (30070154), the Frontier Science Projects Program of the Institute of Hydrobiology, the Chinese Academy of Sciences (220316), State Key Project on Cyanobacterial Bloom Control in Lake Dianchi (K99-05-35-01)Biography: XU Wen-liang (1974-), male, Ph. D, research direction: molecular genetics of cyanobacteria. 展开更多
关键词 anabaena sp. PCC 7120 fecC iron deficiency photosynthetic properties expression
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鱼腥藻SP.595液泡化原生质球诱导条件的研究 被引量:1
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作者 冯武 赵以军 +2 位作者 郭厚良 夏燕华 吴南 《水生生物学报》 CAS CSCD 北大核心 2003年第4期385-389,共5页
用浓度为 0 15mol/L的KNO3 、KCl、K2 SO4、KH2 PO4、K2 HPO4、NaNO3 、NaCl、Na2 SO4、NaH2 PO4、Na2 HPO4、(NH4) 2 SO4、MgSO4、CaCl2 等单盐分别配合 0 1%的溶菌酶处理鱼腥藻sp 5 95 (Anabaenasp 5 95 )。经 4h ,KH2 PO4、K2 SO4... 用浓度为 0 15mol/L的KNO3 、KCl、K2 SO4、KH2 PO4、K2 HPO4、NaNO3 、NaCl、Na2 SO4、NaH2 PO4、Na2 HPO4、(NH4) 2 SO4、MgSO4、CaCl2 等单盐分别配合 0 1%的溶菌酶处理鱼腥藻sp 5 95 (Anabaenasp 5 95 )。经 4h ,KH2 PO4、K2 SO4、Na2 SO4、NaH2 PO4、(NH4) 2 SO4、MgSO4、CaCl2 能诱导形成原生质球 ,但液泡化原生质球极少 ,而KNO3 、NaNO3 、NaCl诱导形成少量液泡化原生质球。用相近浓度的双盐 ,即KNO3 和NaCl、KNO3 和 (NH4) 2 SO4、NaCl和 (NH4) 2 SO4分别配合 0 1%的溶菌酶处理 ,诱导效果亦不佳。用相近浓度的三盐NaCl、KNO3 和 (NH4) 2 SO4及五种盐NaCl、KNO3 、(NH4) 2 SO4、Na2 HPO4和KH2 PO4分别配合 0 1%的溶菌酶处理 ,诱导原生质球和液泡化原生质球的效果明显提高 ,液泡化原生质球比例达到 6 6 90 %— 79 97%。 展开更多
关键词 鱼腥藻 无机盐 原生质球 液泡化 蓝藻
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来源于Thermomyces sp.的植酸酶基因在毕赤酵母中的组成型表达
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作者 张文荟 沈微 +3 位作者 饶志明 诸葛斌 方慧英 诸葛健 《安徽农业科学》 CAS 北大核心 2008年第22期9423-9425,共3页
[目的]研究植酸酶基因在毕赤酵母中的组成型表达。[方法]用PCR方法从嗜热真菌(Thermomyces sp.)中扩增到去除信号肽和内含子后约1.4 kb的phyT基因编码区片段,并对该片段进行克隆与序列测定。[结果]序列相似性分析表明,克隆的植酸酶基因... [目的]研究植酸酶基因在毕赤酵母中的组成型表达。[方法]用PCR方法从嗜热真菌(Thermomyces sp.)中扩增到去除信号肽和内含子后约1.4 kb的phyT基因编码区片段,并对该片段进行克隆与序列测定。[结果]序列相似性分析表明,克隆的植酸酶基因无信号肽和内含子,与报道的嗜热真菌Thermomyces lanuginosus植酸酶基因相似性最高,DNA序列相似性为95%。从验证后的转化子筛选得到了表达嗜热真菌植酸酶的重组毕赤酵母菌株p-phy T,SDS-PAGE分析显示其分子量约为45 kD,重组毕赤酵母成功表达植酸酶。与野生型菌株相比,结果显示重组植酸酶酶活性提高了12.6%,最适温度65℃,75℃仍有64%以上酶活活性;最适pH值为5.5。[结论]嗜热真菌植酸酶基因用组成型质粒能在毕赤酵母中表达。 展开更多
关键词 THERMOMYCES sp. 植酸酶 重组毕赤酵母 热稳定性
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Construction of a Shuttle Vector for Heterologous Gene Expression in Escherichia coli and Microalgae Anabaena 被引量:2
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作者 Donghui Song Jing Li +1 位作者 Xiaoxu Hu Bo Xi 《Engineering(科研)》 2013年第10期540-544,共5页
Theconstruction of an integrative shuttle expression vector and potential utility was reported inEscherichiacoliandAnabaena(Nostoc) sp. strain PCC 7120. The vector comprised of the following elements: (a) an intergeni... Theconstruction of an integrative shuttle expression vector and potential utility was reported inEscherichiacoliandAnabaena(Nostoc) sp. strain PCC 7120. The vector comprised of the following elements: (a) an intergenic non-coding region fromAnabaenato facilitate its genomic integration (b) a strong functional PpsbAIpromoter fromAnabaenafor desired gene expression and (c) neomycin phosphotransferase gene with its own promoter for the selection of transfor-mants. The constructed vectorpAnFP was evaluated by cloning, transfer and expression of thegfpgene encoding green fluorescent protein. When theE.coliandAnabaenasp. strain PCC 7120 were transformed, intensive green fluorescence produced by the products of GFP protein was observed. This result indicated that the integrative shuttle vector pAnFP can be promisingly used in genome transformation for expression of heterologous genes inE.coliand microalgae such asAnabaenaandNostocstrains. 展开更多
关键词 anabaena sp. PCC 7120 INTEGRATIVE SHUTTLE Vector pAnFP GFP Gene
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Construction of PEG-mediated Genetic Transformation and Gene Knockout System in Fusarium oxysporum f. sp.cubense Tropic Race 4 被引量:1
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作者 Lei ZHANG Yan GUO +2 位作者 Yunyue WANG Weihua TANG Sijun ZHENG 《Agricultural Biotechnology》 CAS 2020年第1期15-17,21,共4页
Fusarium wilt of banana, caused by Fusarium oxysporum f. sp. cubense tropic race 4(Foc TR4), is a typical vascular and soil-borne disease which has significantly threatened the sustainable development of banana indust... Fusarium wilt of banana, caused by Fusarium oxysporum f. sp. cubense tropic race 4(Foc TR4), is a typical vascular and soil-borne disease which has significantly threatened the sustainable development of banana industry. In order to reveal the infection process and pathogenesis of Foc TR4, the young mycelia(66.7 mg/ml) of wild-type strain of Foc TR4(WT-Foc TR4) cultured for 18-20 h were lysed with enzyme mixture for protoplast formation, which consisted of 25 mg/ml driselase, 0.4 mg/ml chitinase, 15 mg/ml lysing enzyme and 1.2 mol/L potassium chloride. The resulted protoplasts of 2×10~7 cells/ml were used to test the efficiency of transformation mediated by polyethylene glycol, and up to 9 transformants per microgram of DNA were obtained. AmCyan, RFP and YFP genes were stably transferred into the WT-Foc TR4, separately, using the protoplast transformation system. The gene FoOCH1 encoding α-1, 6-mannosyltransferase in the WT-Foc TR4 was knocked out using the split-marker recombination technology. The genetic transformation and gene knockout system in this pathogen lays a foundation for the study of functional genomics and plant-pathogen interactions. 展开更多
关键词 Fusarium wilt of banana Fusarium oxysporum f.sp.cubense PROTOPLASTS Transformation split-marker recombination
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Insertal Orientation Has No Influence on the Expression of gfp Gene and the Growth of the Host Synechococcus sp.PCC7942
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作者 LU Yongzhong ZHANG Xuecheng 《Journal of Ocean University of China》 SCIE CAS 2006年第1期67-70,共4页
In transgenic process, a foreign gene can be integrated in the host genome in two directions, which may influence its expression. In order to study the effects of insertal orientation, the gfp reporter gene was insert... In transgenic process, a foreign gene can be integrated in the host genome in two directions, which may influence its expression. In order to study the effects of insertal orientation, the gfp reporter gene was inserted in the isiAB locus of Synechococcus sp. PCC7942 in different directions, and the GFP expression levels and the growth of the transgenic algae were compared. It was showed that the gfp gene could express in each direction, and no significant difference was detected on algal growth and GFP expression levels between the two recombinant algae. 展开更多
关键词 orientation effect homologous recombination gfp gene flow cytometry Synechococcus sp. PCC7942
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鱼腥藻PCC7120细胞液泡的初步研究 被引量:10
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作者 郭厚良 金传荫 +3 位作者 浦秋文 宋文贞 周云珍 杨清平 《水生生物学报》 CAS CSCD 北大核心 1999年第4期363-367,共5页
从保存3个月以上的老化培养物中直接检查到游离液泡。液泡为标准圆球状,完全透明,大小相差极为悬殊,多数大型液泡吞噬了数个衰老藻细胞。采用低渗酶解,渗透冲击,低渗酶解和渗透冲击相结合,从培养3个月以上,2个月,1个月,1... 从保存3个月以上的老化培养物中直接检查到游离液泡。液泡为标准圆球状,完全透明,大小相差极为悬殊,多数大型液泡吞噬了数个衰老藻细胞。采用低渗酶解,渗透冲击,低渗酶解和渗透冲击相结合,从培养3个月以上,2个月,1个月,18d,10d及3d的藻丝细胞都分离到液泡。液泡略大于细胞,泡内无吞噬物。培养3d的藻丝有15%的细胞分离到液泡。其他多种蓝藻也分离到同样的液泡。 展开更多
关键词 鱼腥藻PCC7120 液泡 低渗酶解 蓝藻 细胞
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有机碳化合物对鱼腥藻7120生长的影响 被引量:14
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作者 喻国策 丛威 +2 位作者 蔡昭铃 施定基 欧阳藩 《水生生物学报》 CAS CSCD 北大核心 2003年第3期238-242,共5页
在培养基中添加多种有机碳化合物对鱼腥藻 71 2 0进行培养。结果表明 ,葡萄糖的存在能明显地促进细胞的生长 ,但细胞仅能有限地利用葡萄糖 ;细胞混合营养生长的饱和光强约为 80 μEm- 2 s- 1 。乙酸、蔗糖、乙醇和甘油对细胞生长的影响... 在培养基中添加多种有机碳化合物对鱼腥藻 71 2 0进行培养。结果表明 ,葡萄糖的存在能明显地促进细胞的生长 ,但细胞仅能有限地利用葡萄糖 ;细胞混合营养生长的饱和光强约为 80 μEm- 2 s- 1 。乙酸、蔗糖、乙醇和甘油对细胞生长的影响不很显著 ,乳酸、柠檬酸、谷氨酸和甘氨酸表现出明显的抑制作用。鱼腥藻 71 2 0不能利用葡萄糖进行化能异养生长和光激活的化能异养生长 ,但有轻微的光异养现象。 展开更多
关键词 蓝藻 鱼腥藻 有机碳化合物 葡萄糖 混合营养生长 化能异养生长
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不同形态氮对洋河水库螺旋鱼腥藻和惠氏微囊藻生长的影响 被引量:7
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作者 李涵 许秋瑾 +2 位作者 储昭升 张亚丽 蒋丽佳 《环境科学研究》 EI CAS CSCD 北大核心 2010年第12期1494-1498,共5页
利用室内培养试验比较研究了硝酸盐氮和氨氮对洋河水库螺旋鱼腥藻和惠氏微囊藻生长的影响.结果表明:ρ(氨氮)和ρ(硝酸盐氮)均在0.05~10 mg/L内时,螺旋鱼腥藻的生长曲线无显著性差异,氨氮更有利于螺旋鱼腥藻的生长;在0.05~10 mg/L内,... 利用室内培养试验比较研究了硝酸盐氮和氨氮对洋河水库螺旋鱼腥藻和惠氏微囊藻生长的影响.结果表明:ρ(氨氮)和ρ(硝酸盐氮)均在0.05~10 mg/L内时,螺旋鱼腥藻的生长曲线无显著性差异,氨氮更有利于螺旋鱼腥藻的生长;在0.05~10 mg/L内,ρ(氨氮)和ρ(硝酸盐氮)的升高能明显促进惠氏微囊藻的生长,但高浓度的氨氮可能会抑制其生长.当ρ(硝酸盐氮)为0.05 mg/L时,螺旋鱼腥藻比生长速率(0.239 d-1)大于惠氏微囊藻(0.166 d-1);ρ(氨氮)为0.05和0.5mg/L时,螺旋鱼腥藻的比生长速率分别为(0.266±0.012)和(0.303±0.005)d-1,大于惠氏微囊藻的比生长速率(0.096±0.004)和(0.272±0.008)d-1.提示在ρ(氨氮)和ρ(硝酸盐氮)较低的培养条件下,螺旋鱼腥藻比生长速率更高,更易成为优势藻种.洋河水库近2年优势种逐渐从螺旋鱼腥藻转变为惠氏微囊藻,可能是水体中ρ(氮)的变化所致. 展开更多
关键词 螺旋鱼腥藻 惠氏微囊藻 硝酸盐氮 氨氮 比生长速率
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