Application of the FLP/FRT recombination system in cyanobacteria for construction of markerless mutants
文献类型:期刊论文
作者 | Tan, Xiaoming1![]() ![]() |
刊名 | APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
![]() |
出版日期 | 2013-07-01 |
卷号 | 97期号:14页码:6373-6382 |
关键词 | FLP/FRT Cyanobacteria Markerless mutant Marker recycling Genetic engineering Biofuels |
英文摘要 | Due to efficient photosynthetic capability, robust growth, and clear genetic background, cyanobacteria are recently used for production of different biofuel and biochemical molecules by genetic engineering and showed great potentials as the next-generation microbial cell factory. For improving the production of bio-products, a number of genetic modifications are important for cyanobacteria. However, the system-level genetic modification of cyanobacteria is limited by the lack of efficient method for marker recycling. In this investigation, we introduced the self-replicable shutter vectors harboring the flipase (FLP) gene from Saccharomyces cerevisiae into two mutants of Synechocystis sp. PCC6803 and Synechococcus elongatus PCC7942 whose genomes were inserted by a kanamycin resistance gene with flipase recombination target (FRT) flanking, respectively. Transcriptional analysis by reverse transcription polymerase chain reaction showed that FLP gene was transcripted in both the two cyanobacterial strains. Genotyping analysis indicated that FLP performed its function in vivo in both two cyanobacterial strains, and the following DNA sequencing analysis on the targeted loci further confirmed that FLP exactly excised and ligated the two FRT sites between which a kanamycin resistance gene is located. The homozygous mutants free of the kanamycin resistance gene cassette were obtained by conditional expression of FLP and further dilution plating. The shuttle vectors carrying the FLP gene were then lost in these mutants by growing in the absence of antibiotics and the further single colony separation. These results demonstrate that FLP/FRT recombination system is able to be applied to the construction of markerless mutant in both Synechocystis sp. PCC6803 and S. elongatus PCC7942. |
WOS标题词 | Science & Technology ; Life Sciences & Biomedicine |
学科主题 | 生物代谢工程 |
类目[WOS] | Biotechnology & Applied Microbiology |
研究领域[WOS] | Biotechnology & Applied Microbiology |
关键词[WOS] | CARBON-DIOXIDE ; PHOTOSYNTHETIC PRODUCTION ; ESCHERICHIA-COLI ; PCC 6803 ; CONVERSION ; SELECTION ; GENE ; BIOTECHNOLOGY ; PCC-7120 ; ETHYLENE |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000321121800024 |
公开日期 | 2014-03-21 |
源URL | [http://ir.qibebt.ac.cn:8080/handle/337004/1638] ![]() |
专题 | 青岛生物能源与过程研究所_微生物代谢工程团队 |
作者单位 | 1.Chinese Acad Sci, Shandong Prov Key Lab Energy Genet, Qingdao Inst Bioenergy & Bioproc Technol, Key Lab Biofuels, Qingdao 266101, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China |
推荐引用方式 GB/T 7714 | Tan, Xiaoming,Liang, Feiyan,Cai, Ke,et al. Application of the FLP/FRT recombination system in cyanobacteria for construction of markerless mutants[J]. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY,2013,97(14):6373-6382. |
APA | Tan, Xiaoming,Liang, Feiyan,Cai, Ke,&Lu, Xuefeng.(2013).Application of the FLP/FRT recombination system in cyanobacteria for construction of markerless mutants.APPLIED MICROBIOLOGY AND BIOTECHNOLOGY,97(14),6373-6382. |
MLA | Tan, Xiaoming,et al."Application of the FLP/FRT recombination system in cyanobacteria for construction of markerless mutants".APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 97.14(2013):6373-6382. |
入库方式: OAI收割
来源:青岛生物能源与过程研究所
浏览0
下载0
收藏0
其他版本
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。