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Production of γ-linolenic acid and stearidonic acid by Synechococcus sp.PCC7002 containing cyanobacterial fatty acid desaturase genes 被引量:3
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作者 董学卫 何庆芳 +4 位作者 彭振英 于金慧 边斐 李有志 毕玉平 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2016年第4期772-780,共9页
Genetic modifi cation is useful for improving the nutritional qualities of cyanobacteria. To increase the total unsaturated fatty acid content, along with the ratio of ω-3/ω-6 fatty acids, genetic engineering can be... Genetic modifi cation is useful for improving the nutritional qualities of cyanobacteria. To increase the total unsaturated fatty acid content, along with the ratio of ω-3/ω-6 fatty acids, genetic engineering can be used to modify fatty acid metabolism. S ynechococcus sp. PCC7002, a fast-growing cyanobacterium, does not contain a Δ6 desaturase gene and is therefore unable to synthesize γ-linolenic acid(GLA) and stearidonic acid(SDA), which are important in human health. In this work, we constructed recombinant vectors Syd6 D, Syd15 D and Syd6Dd15 D to express the Δ15 desaturase and Δ6 desaturase genes from Synechocystis PCC6803 in Synechococcus sp. PCC7002, with the aim of expressing polyunsaturated fatty acids. Overexpression of the Δ15 desaturase gene in S ynechococcus resulted in 5.4 times greater accumulation of α-linolenic acid compared with the wild-type while Δ6 desaturase gene expression produced both GLA and SDA. Co-expression of the two genes resulted in low-level accumulation of GLA but much larger amounts of SDA, accounting for as much to 11.64% of the total fatty acid content. 展开更多
关键词 synechococcus sp.pcc7002 Synechocystis sp.PCC6803 Δ15 fatty acid desaturase Δ6 fatty acid desaturase polyunsaturated fatty acids
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铁限制诱导对聚球藻转录组的影响 被引量:1
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作者 何昕颖 申铁 《江西师范大学学报(自然科学版)》 CAS 北大核心 2021年第2期180-187,共8页
为探究Fe元素限制对聚球藻转录组的影响,该文以聚球藻Synechococcus sp.PCC 7002为研究对象,采用高通量测序技术对经过铁限制处理的聚球藻Synechococcus sp.PCC 7002进行转录组分析.以铁的3种摩尔浓度进行处理,其中每组数据重复3次实验... 为探究Fe元素限制对聚球藻转录组的影响,该文以聚球藻Synechococcus sp.PCC 7002为研究对象,采用高通量测序技术对经过铁限制处理的聚球藻Synechococcus sp.PCC 7002进行转录组分析.以铁的3种摩尔浓度进行处理,其中每组数据重复3次实验,一共获得9组实验数据;对照组摩尔浓度为10.900 nmol·L^(-1),铁限制组摩尔浓度分别为0.410、0.003 nmol·L^(-1).实验发现:在铁限制环境下,聚球藻通过增加对胞外铁摄取、上调光合作用相关蛋白的表达和调整代谢通路来应对缺铁环境,且铁限制程度与差异基因数量成正相关关系.此外,在强缺铁时通过下调CRISPR系统中某些核酸酶的表达来影响聚球藻抵御外源病毒感染的能力,其转运磷酸基团ABC转运蛋白表达水平下降,从而极大地影响了聚球藻的生存. 展开更多
关键词 聚球藻synechococcus sp.PCC 7002 Fe元素限制 转录组 高通量测序技术
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Heterologous expression of LamA gene encoded endo-β-1,3- glucanase and CO2 fixation by bioengineered Synechococcus sp. PCC 7002 被引量:1
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作者 Di Li Swati Yewalkar +7 位作者 Xiaotao Bi Sheldon Duff Dusko Posarac Heli Wang Layne A. Woodfin Jan-Hendrik Hehemann Sheila C. Potter Francis E. Nano 《Frontiers of Environmental Science & Engineering》 SCIE EI CAS CSCD 2017年第2期115-122,共8页
The gene for the catalytic domain of thermostable endo-β-1,3-glucanase (laminarinase) LamA was cloned from Thermotoga maritima MSB8 and heterologously expressed in a bioengineered Synechococcus sp. PCC 7002. The mu... The gene for the catalytic domain of thermostable endo-β-1,3-glucanase (laminarinase) LamA was cloned from Thermotoga maritima MSB8 and heterologously expressed in a bioengineered Synechococcus sp. PCC 7002. The mutant strain was cultured in a photobioreactor to assess biomass yield, recombinant laminarinase activity, and CO2 uptake. The maximum enzyme activity was observed at a oH of 8.0 and a temoerature of 70℃. At a CO2 concentration of 5%, we obtained a maximum specific growth rate of 0.083 h^-1 a biomass productivity of 0.42 g· L^-1·d^-1 a blomass concentration of 3.697 g.L^-1 , and a specific enzyme activity of the mutant strain of 4.325 U.mg^- 1 dry mass. All parameters decreased as CO2 concentration increased from 5% to 10% and further to 15% CO2, except enzyme activity, which increased from 5% to 10% CO2. However, the mutant culture still 1 1 grew at 15% CO2 concentration, as reflected by the blomass productwlty (0.26 g.L .d ), biomass concentration (2.416 g.L^- 1), and specific enzyme activity (3.247 U.mg^-1 dry mass). 展开更多
关键词 synechococcus sp. PCC 7002Thermotoga maritimaLamA geneEndo-β-1 3-glucanaseCO2 fixation
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Development of an activity-directed selection system enabled significant improvement of the carboxylation efficiency of Rubisco 被引量:17
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作者 Zhen Cai Guoxia Liu +1 位作者 Junli Zhang Yin Li 《Protein & Cell》 SCIE CAS CSCD 2014年第7期552-562,共11页
Photosynthetic CO2 fixation is the ultimate source of organic carbon on earth and thus is essential for crop production and carbon sequestration, Ribulose-1,5-bis- phosphate carboxylase/oxygenase (Rubisco) catalyzes... Photosynthetic CO2 fixation is the ultimate source of organic carbon on earth and thus is essential for crop production and carbon sequestration, Ribulose-1,5-bis- phosphate carboxylase/oxygenase (Rubisco) catalyzes the first step of photosynthetic CO2 fixation. However, the extreme low carboxylation efficiency of Rubisco makes it the most attractive target for improving pho- tosynthetic efficiency. Extensive studies have focused on re-engineering a more efficient enzyme, but the effort has been impeded by the limited understanding of its structure-function relationships and the lack of an effi- cient selection system towards its activity. To address the unsuccessful molecular engineering of Rubisco, we developed an Escherichia coil-based activity-directed selection system which links the growth of host cell solely to the Rubisco activity therein. A Synechococcus sp. PCC7002 Rubisco mutant with E49V and D82G sub- stitutions in the small subunit was selected from a total of 15,000 mutants by one round of evolution. This mutant showed an 85% increase in specific carboxyla- tion activity and a 45% improvement in catalytic efficiency towards CO2. The small-subunit E49V mutation was speculated to influence holoenzyme catalysis through interaction with the large-subunit Q225. This interaction is conserved among various Rubisco from higher plants and Chlamydomonas reinhardtii. Knowledge of these might provide clues for engineering Rubisco from higher plants, with the potential of increasing the crop yield. 展开更多
关键词 carboxylation efficiency CO2 fixation directed evolution RUBISCO synechococcus sp. pcc7002
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