参考文献/References:
[1]STOLS L, GU M, DIECKMAN L, et al. A new vector for high-throughput, ligation-independent cloning encoding a tobacco etch virus protease cleavage site[J]. Protein Expression and Purification, 2002, 25(1): 8-15.
[2]DIECKMAN L, GU M, STOLS L, et al. High throughput methods for gene cloning and expression[J]. Protein Expression and Purification, 2002, 25(1): 1-7.
[3]CHEO D L, TITUS S A, BYRD D R N, et al. Concerted assembly and cloning of multiple DNA segments using in vitro site-specific recombination: functional analysis of multi-segment expression clones[J]. Genome Research, 2004, 14(10b): 2111-2120.
[4]ASLANIDIS C, DE JONG P J. Ligation-independent cloning of PCR products (LIC-PCR)[J]. Nucleic Acids Research, 1990, 18(20): 6069-6074.
[5]CHAN J, MAO G, SMERTENKO A, et al. Identification of a MAP65 isoform involved in directional expansion of plant cells[J]. FEBS Letters, 2003, 534(1-3): 161-163.
[6]SMERTENKO A P, CHANG H Y, WAGNER V, et al. The Arabidopsis microtubule-associated protein AtMAP65-1: molecular analysis of its microtubule bundling activity[J]. The Plant Cell, 2004, 16(8): 2035-2047.
[7]CHANG-JIE J, SONOBE S. Identification and preliminary characterization of a 65 kDa higher-plant microtubule-associated protein[J]. Journal of Cell Science, 1993, 105(4): 891-901.
[8]HUSSEY P J, HAWKINS T J, IGARASHI H, et al. The plant cytoskeleton: recent advances in the study of the plant microtubule-associated proteins MAP-65, MAP-190 and the Xenopus MAP215-like protein, MOR1[J]. Plant Molecular Biology, 2002, 50(6): 915-919.
[9]MAO T, JIN L, LI H, et al. Two microtubule-associated proteins of the Arabidopsis MAP65 family function differently on microtubules[J]. Plant Physiology, 2005, 138(2): 654-662.
[10]SMERTENKO A P, CHANG H Y, SONOBE S, et al. Control of the AtMAP65-1 interaction with microtubules through the cell cycle[J]. Journal of Cell Science, 2006, 119(15): 3227-3237.
[11]LI H, ZENG X, LIU Z Q, et al. Arabidopsis microtubule-associated protein AtMAP65-2 acts as a microtubule stabilizer[J]. Plant Molecular Biology, 2009, 69(3): 313-324.
[12]栗华.两种拟南芥微管结合蛋白AtMAP65-1和AtMAP65-2的功能分析[D].北京:中国农业大学, 2007.
[13]韩榕,王勋陵,岳明,等. 增强UV-B 辐射对小麦体细胞分裂的影响[J]. 遗传学报, 2002, 29(6): 537-541.
[14]CHANDA P K, EDRIS W A, KENNEDY J D. A set of ligation-independent expression vectors for co-expression of proteins in Escherichia coli[J]. Protein Expression and Purification, 2006, 47(1): 217-224.
[15]WEEKS S D, DRINKER M, LOLL P J. Ligation independent cloning vectors for expression of SUMO fusions[J]. Protein Expression and Purification, 2007, 53(1): 40-50.
[16]DONNELLY M I, ZHOU M, MILLARD C S, et al. An expression vector tailored for large-scale, high-throughput purification of recombinant proteins[J]. Protein Expression and Purification, 2006, 47(2): 446-454.
[17]TAN R, MA L. Novel ligation-independent cloning vectors for production of native proteins[J]. Journal of Hubei University (Natural Science), 2009, 4: 22.
[18]CABRITA L D, DAI W, BOTTOMLEY S P. A family of E. coli expression vectors for laboratory scale and high throughput soluble protein production[J]. BMC Biotechnology, 2006, 6(1): 12.
[19]DAN H, BALACHANDRAN A, LIN M. A pair of ligation-independent Escherichia coli expression vectors for rapid addition of a polyhistidine affinity tag to the N-or C-termini of recombinant proteins[J]. Journal of Biomolecular Techniques JBT, 2009, 20(5): 241.
[20]ESCHENFELDT W H, LUCY S, MILLARD C S, et al. A family of LIC vectors for high-throughput cloning and purification of proteins[J]. High Throughput Protein Expression and Purification: Methods and Protocols, 2009, 498: 105-115.
[21]刘超,林陈水. 不依赖于连接反应克隆 (LIC) 的技术进展[J]. 基因组学与应用生物学, 2011, 30: 1081-1085.
相似文献/References:
[1]夏雯雯,李锦,祝建波.天山雪莲水孔蛋白基因(AQP)家族鉴定与生物信息学分析[J].江苏农业学报,2016,(06):1244.[doi:doi:10.3969/j.issn.1000-4440.2016.06.008]
XIA Wen-wen,LI Jin,ZHU Jian-bo.Identification and bioinformatics analysis of aquaporin gene (AQP) family in Saussurea involucrate Kar.[J].,2016,(02):1244.[doi:doi:10.3969/j.issn.1000-4440.2016.06.008]
[2]余璐璐,龚绒雪,吕林涛,等.拟南芥氰丙氨酸合酶CYS-C1基因扩增及多克隆抗体制备[J].江苏农业学报,2017,(06):1235.[doi:doi:10.3969/j.issn.1000-4440.2017.06.006]
YU Lu-lu,GONG Rong-xue,LYU Lin-tao,et al.Cyanoalanine synthase CYS-C1 gene amplification and polyclonal antibody preparation in Arabidopsis thaliana[J].,2017,(02):1235.[doi:doi:10.3969/j.issn.1000-4440.2017.06.006]
[3]王津,韩榕.DNA甲基转移酶赋予拟南芥盐胁迫耐受性[J].江苏农业学报,2019,(05):1028.[doi:doi:10.3969/j.issn.1000-4440.2019.05.004]
WANG Jin,HAN Rong.DNA methyltransferases confer salt stress tolerance in Arabidopsis thaliana[J].,2019,(02):1028.[doi:doi:10.3969/j.issn.1000-4440.2019.05.004]
[4]高营,林云,袁星星,等.蚕豆VfGASA1基因的异源过表达延迟拟南芥开花[J].江苏农业学报,2021,(01):44.[doi:doi:10.3969/j.issn.1000-4440.2021.01.006]
GAO Ying,LIN Yun,YUAN Xing-xing,et al.Heterologous overexpression of Vicia faba VfGASA1 gene delays flowering in transgenic Arabidopsis[J].,2021,(02):44.[doi:doi:10.3969/j.issn.1000-4440.2021.01.006]
[5]徐雪珍,郑月萍,张夏婷,等.拟南芥AtFAD6基因突变体的构建[J].江苏农业学报,2021,(05):1125.[doi:doi:10.3969/j.issn.1000-4440.2021.05.005]
XU Xue-zhen,ZHENG Yue-ping,ZHANG Xia-ting,et al.Construction of Arabidopsis AtFAD6 gene mutant[J].,2021,(02):1125.[doi:doi:10.3969/j.issn.1000-4440.2021.05.005]