[1]Kindle K L.High-frequency nuclear transformation of Chlamydo-monas reinhardtii J].PNAS,1990 (87):1228.
[2]黄非,黄秦,黄敏,等。莱茵衣藻玻璃珠法快速转化检测体系的建立[J].四川大学学报(自然科学版),2008(03):694-698.
[3]Shimogawara K,Fujiwara S,Grossman A,et al.High-efficiencytransformation of Chlamydomonasreinhardtii byelectroporation J].Genetics,1998,148(4):1821-1828.
[4]Takashi Y,Hiro I,Hideya F.Rapid transformation of Chlamydo-monas reinhardtii without cell-wallremoval[J].Joural of Biosci-ence and Bioengineering,2013,115 (6):691-694.
[5]Wang L,Yang L J,Wen X,et al.Rapid and high efficiencytransformation of Chlamydomonas reinhardtiiby square-wave elec-troporation [J].BioscienceReports,2019,39 (1):BSR20181210.
[6]宋程飞,郝敬云,程蔚兰,等.杜氏盐藻电击转化体系的优化[J].山西农业大学学报(自然科学版),2018,38(03):36-42.
[7]刘佳,何炫程,项晨,等.一种高效的莱茵衣藻电转化方法[J].北京农学院学报,2019,34(02):5-9.
[8]Klein T M,Wolf E D,Wu R,et al.High-velocity microprojec-tiles for delivering nucleic acids into living cells [J].Nature,1987,327:70-73.
[9]Wannathong T,Waterhouse J C,Young R E B,et al.New toolsfor chloroplast genetic engineering allow the synthesis of humangrowth hormone in the green alga Chlamydomonas reinhardtii [J].Applied Microbiology and Biotechnology,2016,100 (12):5467-5477.
[10]Kindle K L,Schnell R A,Femandez,PA.Lefebvre,Stablenuclear transformation of Chlamydomonas using the Chlamydomonasgene for nitrate reductase [J ]Cell Biol.1989,109 (6):2589-2601.
[11]Debuchy R,Purton S,Rochaix J D,et al.The argininosuccinatelyase gene of Chlamydomonas reinhardtii:an important tool for nu-clear transformation and for correlating the genetic and molecular maps of the ARG7 locus J].EMBO J,1989,8 (10):2803-2809.
[12]闫晋飞.利用基因工程手段提高两种微藻的生物量与特定代谢产物产量[D].沈阳:沈阳药科大学,2013.
[13]陈禹先,毕丛斌,佟少明,等.微藻高效基因枪转化方法的建立[J].中国生物化学与分子生物学报,2018,34(07):794-800.
[14]Hadi M Z,McMullen M D,Finer JJ.Transformation of 12 dif-ferent plasmids into soybean via particle bombardment [J].PlantCell Reports,.1996,15(7):500-505.
[15]Kumar S V,Misquitta R W,Reddy V S,et al.Genetic transfor-mation of the green alga-Chlamydomonasreinhardtii by Agrobacteriumtumefaciens [J].Plant Science,2004,166 (3):731-738.
[16]郭娟娟,李江洪,龙婷婷,等.农杆菌介导小球藻快速转化方法的建立与条件优化[J].中国酿造,2021,40(04):56-60.
[17]Mini P,Demurtas O C,Valentini S,et al.Agrobacterium-me-diated and electroporation-mediatedtransformation of Chlamydo-monas reinhardtii:a comparative study [J].BMC Biotechnology,2018,18(1):1-12.
[18]Debuchy R,Purton S,Rochaix J D.The argininosuccinate lyasegene of Chlamydomonas reinhardtii:an important tool for nucleartransformation and for correlating the genetic and molecular maps ofthe ARG7 locus[J].EMB0J,1989,8(10):2803-2809.
[19]陈秦.浮丝藻中微囊藻毒素基因的检测技术及在环境中变异研究[D].咸阳:西北农林科技大学,2017.
[20]Heitzer M,Zschoernig B.Construction of modular tandem expressionvectors for the green alga Chlamydomona reinhardtii using the Cre/lox-system [J].Biotechniques,2007,43 (3):324,326,328.
[21]Dunahay T G.Transformation of Chlamydomonas reinhardtii withsilicon carbide whiskers [J].Biotechniques,1993,15:452-455,457-458,460.
[22]Felgner P L,Gadek T R,Holm M,et al.Lipofection:a highlyefficient,lipid-mediated DNA-transfection procedure J].Pro-ceedings of the National Academy of Sciences of USA,1987,84(21):7413-7417.
[23]Kim S,Lee Y C,Cho D H,et al.A simple and non-invasivemethod for nuclear transformation of intact-walled Chlamydomonas reinhardtii [J].PLoS One,2014,9:e101018.
[24]黄亚萍,艾丽,王川.莱茵衣藻细胞核转化体系研究进展[J].生物技术,2017,27(06):601-606.
[25]闫晋飞,杨玉莹,马淑霞.微藻基因工程概述[J].生物学报,2017,52(04):1-5.
[26]Shi Q W,Chen C,Zhang W,et al.Transgenic eukaryotic mi-croalgae as green factories:providing new ideas for the productionof biologically active substances [J].Joumal of Applied Phycolo-gy,2021,33(2):705-728.
[27]徐晓婷,减晓南,章峰,等.别藻蓝蛋白B亚基基因在莱茵衣藻中重组表达及其对光能传递的影响研究[J].中国海洋大学学报(自然科学版),2023,53(09):77-88.
[28]Guo S L,Zhao X Q,Tang Y,et al.Establishment of an efficientgenetic transformation system in Scenedesmus obliquus [J].Jour-nal of Biotechnology,2013,163 (1):61-68.
[29]Specht E A.Improving the genetic tractability of the green algaChlamydomonas reinhardtii D].2014.
[30]朱振,田晶,江静,等.微藻叶绿体细胞器工厂研究进展[J].合成生物学,2022,3(06):1218-1234.
[31]Siddiqui A,Wei Z Y,Boehm M,et al.Engineering microalgaethrough chloroplast transformation to produce high-value industrialproducts [J].Biotechnol Appl Biochem,2020,67 (1):30-40.
[32]Lorena AA,Flores-Uribe J,Hugo Perez-Espana V,et al.Pro-duction of therapeutic proteins in the chloroplast of Chlamydomonasreinhardtii [J].AMb Express,2014,4 (1):57.
[33]Coragliotti A T,Beligni M V,Franklin S E,et al.Molecularfactors affecting the accumulation of recombinant proteins in theChlamydomonas reinhardtii chloroplast J].Mol Biotechnol,2011,48(1):60-75.
[34]Rasala B A,Muto M,Sullivan J,et al.Improved heterologousprotein expression in the chloroplast of Chlamydomonas reinhardtiithrough promoter and 5'untranslated region optimization J].Plant Biotechnology Journal,2011,9 (6):674-683.
[35]Boynton J E,Gillham N W,Harris E H,et al.Chloroplasttransformation in Chlamydomonas with high velocity microprojec-tiles[J].Science,1988,240(4858):1534-1538.
[36]Stoffels L,Taunt H N,Charalambous B,et al.Synthesis of bac-teriophage lytic proteins against Streptococcus pneumoniae in thechloroplast of Chlamydomonas reinhardtii [J].Plant Biotechnolo-gy Joural,2017,15(9):1130-1140.
[37]Grant D,Chiang K S.Physical mapping and characterization ofChlamydomonas mitochondrial DNA molecules:their unique ends,sequence homogeneity,and conservation [J].Plasmid,1980,4(1):82-96.
[38]Kuick U,Neuhaus H.Universal genetic code evidenced in mito-chondria of Chlamydomonas reinhardtii [J].Applied Microbiologyand Biotechnology,1986,23:462-469.
[39]Randolph-Anderson B L,Boynton J E,Gillham N W,et al.Further characterization of the respiratory deficient dum-1 mutationof Chlamydomonas reinhardtii and its use as a recipient for mito-chondrial transformation J].Molecular and General Genetics,1993,236(2-3):235-244
[40]李建成,彭世清,胡章立.SEC2在莱茵衣藻中表达及免疫学活性分析[J].深圳大学学报理工版,2012,29(02):159-164. |