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小鼠金属硫蛋白在聚胞藻中的金属诱导表达与纯化 被引量:14
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作者 郭祥学 赵晖 +2 位作者 施定基 徐旭东 茹炳根 《生物工程学报》 CAS CSCD 北大核心 1998年第4期405-411,共7页
应用蓝藻类金属硫蛋白基因启动子(smtOP)的金属诱导性,在单细胞的聚胞藻PCC6803中表达小鼠金属硫蛋白结构基因(mMT1cDNA)。在大肠杆菌HB101中构建含有smtOP和mMT1cDNA的穿梭表达载... 应用蓝藻类金属硫蛋白基因启动子(smtOP)的金属诱导性,在单细胞的聚胞藻PCC6803中表达小鼠金属硫蛋白结构基因(mMT1cDNA)。在大肠杆菌HB101中构建含有smtOP和mMT1cDNA的穿梭表达载体pKTMRE,经质粒转移,链霉素筛选,Southern和Western杂交分析鉴定得稳定的转基因工程藻落。同时,做小批量锌诱导表达,并纯化了外源蛋白,5L培养液含鲜藻重50g,得到35mgmMT1;转基因藻在高金属浓度下的耐受性测定表明,外源基因的表达提高了蓝藻对金属离子的抗性,约为野生藻的2倍。 展开更多
关键词 聚胞藻PCC6803 smtO-P区域 金属硫蛋白
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聚胞藻热模拟产烃研究 被引量:6
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作者 王睿勇 周文 +2 位作者 吴庆余 盛国英 傅家谟 《南京大学学报(自然科学版)》 CAS CSCD 1999年第5期525-531,共7页
采用GC和GCMS对蓝藻聚胞藻原生烃类及热解烃类进行了分析.聚胞藻在250 ℃~300 ℃热解产气属于低熟气,以非烃气为主,产气组分参数反映了原核生物母质来源的特征.热解作用使其氯仿沥青“A”含量和烷烃含量大幅度提高... 采用GC和GCMS对蓝藻聚胞藻原生烃类及热解烃类进行了分析.聚胞藻在250 ℃~300 ℃热解产气属于低熟气,以非烃气为主,产气组分参数反映了原核生物母质来源的特征.热解作用使其氯仿沥青“A”含量和烷烃含量大幅度提高.原生烷烃以正烷烃为主,主峰为nC17 .热解烷烃仍以低碳数正烷烃为主,主峰为nC17 ,反映了典型的藻类母质来源的烷烃特征.热解烷烃中还检出了丰富的二环倍半萜和五环三萜.五环三萜以C30 莫烷为主峰,并含有丰度较高的C30藿烯。 展开更多
关键词 聚胞藻 热模拟成烃 烷烃生物标志物 烃类 低熟油
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生物防治
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《生物技术通报》 CAS CSCD 1995年第1期85-87,共3页
专利内容为一种商业化规模生产具有阔叶锦葵(Malua pusilla)除莠活性的真菌制品的方法。
关键词 苏云金芽孢杆菌以色列亚种 启动子 PCC7942 几丁酶 杀虫晶体蛋白 除莠活性 玉米螟 表达载体 聚胞藻PCC6803 转基因植物
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Toxicity and Accumulation of Selenite in Four Microalgae 被引量:1
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作者 王大志 程兆第 +1 位作者 李少菁 高亚辉 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2003年第3期280-285,共6页
The toxicity and bioaccumulation of selenite in four microalgae, Spirulina platensis, Dunaliella salina, Dunaliella bardawill and Phaeodactylum tricornutum cultured in the presence of selenite were investigated. Lower... The toxicity and bioaccumulation of selenite in four microalgae, Spirulina platensis, Dunaliella salina, Dunaliella bardawill and Phaeodactylum tricornutum cultured in the presence of selenite were investigated. Lower concentrations of selenite were generally nontoxic and frequently stimulated algal growth, while higher concentrations of selenite inhibited algal growth. Selenite was more toxic to D. salina and D. bardawill than to S. platensis and P. tricornutum . All algae cultured in selenite were able to incorporate Se to different degrees, which depended on algal species. The distributions of selenite among intracellular macromolecular compounds were different among algal species: most of the selenite was associated with proteins in S. platensis, D. salina and D. bardawill , while most of the selenite was associated with lipids in P. tricornutum , which reflected the physiological differences among the algae. These observations suggest that algae are able to accumulate selenite and bind it with intracellular macromolecular compounds when exposed to high concentration of selenite. This may represent a form of storage or detoxification of selenite by the algae. 展开更多
关键词 SELENITE MICROALGAE TOXICITY accumulation intracellular distribution
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Live imaging of the effects of fucoidan on cell proliferation for laboratory instruction
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作者 Hong Wu 《TMR Theory and Hypothesis》 2018年第2期45-50,共6页
The aim of this study is to introduce live cell imaging and its applications for the evaluation of the effects of fucoidan, a fucose-enriched sulfated polysaccharide, on the proliferation of cultured cells in vitro. I... The aim of this study is to introduce live cell imaging and its applications for the evaluation of the effects of fucoidan, a fucose-enriched sulfated polysaccharide, on the proliferation of cultured cells in vitro. In this study, long-term time- lapse observation (87 h) of the effects of fucoidan was conducted using BioStation CT, an integrated cell culture observation system. In contrast, the effects of heparin, which has a similar structure to fucoidan, were observed to distinguish the differences between the two chemicals. At the same time, the viability of the floating cells detached by fucoidan in the medium was measured by culturing them again in the absence of fucoidan. Finally, total internal reflection fluorescence microscopy (TIRF) was used to confirm when the detachment of the cells by fucoidan occurred. The results indicate that the inhibitory effects of fucoidan on the proliferation of cells are dose-dependent (from 0.125 mg/ml to 1.0 mg/ml). Fucoidan also causes cell detachment without killing all the cells within 24 hours. The cell detachment did not occur until after half an hour, as observed under the TIRF microscope. Combined with our previous study, the findings suggest that the inhibition of calcium responses by fucoidan may be one of the mechanisms underlying its inhibition of cell proliferation, which is responsible for the death of cancer cells. Cell proliferation can be visualized in the real time and the images can provide important information regarding when and how the cells grow and proliferate. 展开更多
关键词 Live cell imaging TIME-LAPSE Cell proliferation FUCOIDAN
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