Please wait a minute...
Journal of Integrative Agriculture  2013, Vol. 12 Issue (12): 2134-2142    DOI: 10.1016/S2095-3119(13)60567-5
Crop Genetics · Breeding · Germplasm Resources Advanced Online Publication | Current Issue | Archive | Adv Search |
Optimization of Agrobacterium tumefaciens-Mediated Immature Embryo Transformation System and Transformation of Glyphosate-Resistant Gene 2mG2-EPSPS in Maize (Zea mays L.)
 YUGui-rong12, LIUYan3, DUWen-ping2, SONGJun2, LINMin4, XULi-yuan2, XIAOFang-ming5
 YUGui-rong12, LIUYan3, DUWen-ping2, SONGJun2, LINMin4, XULi-yuan2, XIAOFang-ming5
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
摘要  Since maize is one of the most important cereal crops in the world, establishment of an efficient genetic transformation system is critical for its improvement. In the current study, several elite corn lines were tested for suitability of Agrobacterium tumefaciens-mediated transformation by using immature embryos as explants. Infection ability and efficiency of transformation of A. tumefaciens sp. strains EHA105 and LBA4404, different heat treatment times of immature embryos before infection, influence of L-cysteine addition in co-cultivation medium after transformation, and how different ways of selection and cultivation influence the efficiency of transformation were compared. Glyphosate-resistant gene 2mG2-EPSPS was transformed into several typical maize genotypes including 78599, Zong 31 and BA, under the optimum conditions. Results showed that the hypervirulent Agrobacterium tumefaciens sp. strain EHA105 was more infectious than LBA4404. Inclusion of L-cysteine (100 mg L-1) in co-cultivation medium, and heating of the immature embryos for 3 min prior to infection led to a significant increase in the transformation efficiency. Growth in resting medium for 4-10 d and delaying selection was beneficial to the survival of resistant calli. During induction of germination, adding a high concentration of 6-BA (5 mg L-1) and a low concentration of 2,4-D (0.2 mg L-1) to regeneration medium significantly enhanced germination percentage. Using the optimized transformation procedure, more than 800 transgenic plants were obtained from 78599, Zong 31 and BA. By spraying herbicide glyphosate on leaves of transgenic lines, we identified 66 primary glyphosate-resistant plants. The transformation efficiency was 8.2%. PCR and Southern-blot analyses confirmed the integration of the transgenes in the maize genome.

Abstract  Since maize is one of the most important cereal crops in the world, establishment of an efficient genetic transformation system is critical for its improvement. In the current study, several elite corn lines were tested for suitability of Agrobacterium tumefaciens-mediated transformation by using immature embryos as explants. Infection ability and efficiency of transformation of A. tumefaciens sp. strains EHA105 and LBA4404, different heat treatment times of immature embryos before infection, influence of L-cysteine addition in co-cultivation medium after transformation, and how different ways of selection and cultivation influence the efficiency of transformation were compared. Glyphosate-resistant gene 2mG2-EPSPS was transformed into several typical maize genotypes including 78599, Zong 31 and BA, under the optimum conditions. Results showed that the hypervirulent Agrobacterium tumefaciens sp. strain EHA105 was more infectious than LBA4404. Inclusion of L-cysteine (100 mg L-1) in co-cultivation medium, and heating of the immature embryos for 3 min prior to infection led to a significant increase in the transformation efficiency. Growth in resting medium for 4-10 d and delaying selection was beneficial to the survival of resistant calli. During induction of germination, adding a high concentration of 6-BA (5 mg L-1) and a low concentration of 2,4-D (0.2 mg L-1) to regeneration medium significantly enhanced germination percentage. Using the optimized transformation procedure, more than 800 transgenic plants were obtained from 78599, Zong 31 and BA. By spraying herbicide glyphosate on leaves of transgenic lines, we identified 66 primary glyphosate-resistant plants. The transformation efficiency was 8.2%. PCR and Southern-blot analyses confirmed the integration of the transgenes in the maize genome.
Keywords:  maize       immature embryo       Agrobacterium tumefaciens-mediated transformation       transgenic approach       glyphosate resistance  
Received: 12 November 2012   Accepted:
Fund: 

The study was supported by the National Key Project of transgenic varieties breeding (2009ZX08003-003B), the Light of West Talent Training Project of China (2010- 2011) and the Project of Sichuan Province Finance Genetic Engineering, China (2011JYGC01-002).

Corresponding Authors:  LIU Yong-sheng, E-mail: liuyongsheng1122@hfut.edu.cn     E-mail:  liuyongsheng1122@hfut.edu.cn
About author:  YU Gui-rong, E-mail: yuguirong@163.com

Cite this article: 

YUGui-rong12 , LIUYan3 , DUWen-ping2 , SONGJun2 , LINMin4 , XULi-yuan2 , XIAOFang-ming5 . 2013. Optimization of Agrobacterium tumefaciens-Mediated Immature Embryo Transformation System and Transformation of Glyphosate-Resistant Gene 2mG2-EPSPS in Maize (Zea mays L.). Journal of Integrative Agriculture, 12(12): 2134-2142.

[1]Armstrong C L, Green C E. 1985. Establishment and maintenance of friable embryogenic maize callus and the involvement of L-proline. Planta, 164, 207-214

[2]Brettschneider R, Becker D, Lorz H 1997. Efficient transformation of scutellar tissue of immature maize embryos. Theoretical and Applied Genetics, 94, 737- 748.

[3]Cheng M, Jarret R L, Li Z, Xing A, Demski J W. 1996. Production of fertile transgenic peanut (Arachis kypogaea L.) plants using Agrobacterium tumefaciens. Plant Cell Reports, 15, 653-657

[4]Dong S J, Qu R D 2005. High efficiency transformation of tall fescue with Agrobacterium tumefaciens. Plant Science, 168, 1453-1458

[5]Green C E, Phillips R L 1975. Plant regeneration from tissue cultures of maize. Crop Science, 15, 417-421

[6]Hiei Y, Ohta S, Komari T, Kumashiro T 1994. Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. The Plant Joural, 6, 271-282

[7]Howe A, Sato S, Dweikat I, Fromm M, Clemente T 2006. Rapid and reproducible Agrobacterium-mediated transformation of sorghum. Plant Cell Reports, 25, 784- 791.

[8]Huang X, Wei Z. 2005. Successful Agrobacterium-mediated genetic transformation of maize elite inbred lines. Plant Cell, Tissue and Organ Culture, 83, 187-200

[9]Huang Y H, Zhou M P, Ye X G, Tang K X, Cheng H M, Lu W Z. 2002. Study on the development of transgenic wheat mediated by Agrobacterium tumefaciens. Acta Agronomica Sinica, 28, 510-515 (in Chinese)

[10]Ishida Y, Saito H, Ohta S, Hiei Y, Komari T, Kumashiro T. 1996. High efficiency transformation of maize (Zea mays L.) mediated by Agrobacterium tumefaciens. Nature Biotechnology, 14, 745-750

[11]Jefferson R A, Kavanagh T A, Bevan M W. 1987. GUS- fusions: β-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO Journal, 6, 3901- 3907.

[12]Murray M G, Thompson W F. 1980. Rapid isolation of highmolecular-weight plant DNA. Nucleic Acids Research, 8, 4321-4325

[13]Pareddy D R, Petolino J F. 1990. Somatic embryogenesis and plant regeneration from immature inflorescences of several elite inbreds of maize. Plant Science, 67, 211- 219.

[14]Ray D S, Ghosh P D. 1990. Somatic embryogenesis and plant regeneration from cultured leaf explants of Zea mays. Annals of Botany, 66, 497-500

[15]Rhodes C A, Green C E, Phillips R L. 1986. Factors affecting tissue culture initiation from maize tassels. Plant Science, 46, 225-232

[16]Sambrook J, Fritsch E F, Maniatis T. 1989. Molecular Cloning: A Laboratory Manual. 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.

[17]Santos M A, Torne J M, Blanco J L. 1984. Methods of obtaining maize totipotent tissues I: seedling segments culture. Plant Science Letter, 33, 309-315

[18]Schlappi M, Hohn B. 1992. Competence of immature maize embryos for Agrobacterium mediated gene transfer. The Plant Cell, 4, 7-16

[19]Schroeder H E, Schotz A H, Wardley-Richardson T, Spencer D, Higgins T J V. 1993. Transformation and regeneration of two cultivars of pea (Pisum sativum L.). Plant Physiology, 101, 751-757

[20]Songstad D D, Peterson W L, Armstrong C L. 1992. Establishment of friable embryogenic (type II) callus from immature tassels of Zea mays (Poaceae). American Journal of Botany, 79, 761-764

[21]Suprasanna P, Rao K V, Reddy G M. 1986. Plantlet regeneration from glume calli of maize (Zea mays L.). Theoretical and Applied Genetics, 72, 120-122

[22]Ting Y C, Yu M, Wan Z Z. 1981. Improved anther culture of maize (Zea mays L.). Plant Science Letter, 23, 139- 145.

[23]Umbeck P, Swain W, Yang N S. 1989. Inheritance and expression of genes for kanamycin and chloramphenicol resistance in transgenic cotton plants. Crop Science, 29, 196-201

[24]Vasil V, Vasil I K, Lu C. 1984. Somatic embryogenesis in long term callus cultures of Zea mays L. (Gramineae). American Journal of Botany, 71, 158-161

[25]Wang J X, Sun Y, Li Y. 2007. Maize (Zea mays) genetic transformation by co-cultivating germinating seeds with Agrobacterium tumefaciens. Biotechnology and Applied Biochemistry, 46, 51-55(in Chinese)

[26]Wang X H, Bai J R, Sun Y, Shi X Y, Ren Z Q. 2010. Study on Agrobacterium tumefaciens-mediated glyphosate- resistant gene (EPSPS) transformation and correlation factor in maize. Journal of Shanxi Agricultural Scienses, 38, 11-14 (in Chinese)

[27]Yang A G. 2006. Study one the optimization of the maize callus genetic transformation system mediated by Agrobacterium and the male sterile line in genetic engineering. PhD thesis, Sichuan Agricultural University, China. (in Chinese)

[28]Yuan Y, Li Q Y, Hao W Y. 2006. Studies on influencing factors of Agrobacterium tumefaciens mediated maize transformation. Molecular Plant Breeding, 14, 228-232

[29]Z h a n g S, Williams-Carrier, Lemaux P G. 2002. Transformation of recalcitrant maize elite inbreds using in vitro shoot meristematic cultures induced from germinated seedlings. Plant Cell Reports, 21, 263-270

[30]Zhang S Z, Rong T Z. 2008. Advance of Agrobaterium-mediated genetic transformation system of maize (Zea mays L.). Hereditas, 30, 1249-1256

[31]Zhao Z Y, Gu W, Cai T, Tagliani L, Hondred D, Bond D, Schroeder S, Rudert M, Pierce D. 2002. High throughput genetic transformation mediated by Agrobacterium tumefaciens in maize. Molecular Breed, 8, 323-333

[32]Zhong H, Srinivasan C, Sticklen M B. 1992. In-vitro morphogenesis of corn (Zea mays L.). Planta, 187, 483- 489.

[33]Zhu Y. 2002. Identification of glyphsate-tolerant Psedomonas fluorescens strain G2 from extremly polluted environment and cloning of its EPSP synthase gene. MSc thesis, Chinese Academy of Agricultural Sciences, China. (in Chinese)
[1] Peng Liu, Langlang Ma, Siyi Jian, Yao He, Guangsheng Yuan, Fei Ge, Zhong Chen, Chaoying Zou, Guangtang Pan, Thomas Lübberstedt, Yaou Shen. Population genomic analysis reveals key genetic variations and the driving force for embryonic callus induction capability in maize[J]. >Journal of Integrative Agriculture, 2024, 23(7): 2178-2195.
[2] Jiang Liu, Wenyu Yang. Soybean maize strip intercropping: A solution for maintaining food security in China[J]. >Journal of Integrative Agriculture, 2024, 23(7): 2503-2506.
[3] Hui Fang, Xiuyi Fu, Hanqiu Ge, Mengxue Jia, Jie Ji, Yizhou Zhao, Zijian Qu, Ziqian Cui, Aixia Zhang, Yuandong Wang, Ping Li, Baohua Wang. Genetic analysis and candidate gene identification of salt tolerancerelated traits in maize[J]. >Journal of Integrative Agriculture, 2024, 23(7): 2196-2210.
[4] Hui Chen, Hongxing Chen, Song Zhang, Shengxi Chen, Fulang Cen, Quanzhi Zhao, Xiaoyun Huang, Tengbing He, Zhenran Gao. Comparison of CWSI and Ts-Ta-VIs in moisture monitoring of dryland crops (sorghum and maize) based on UAV remote sensing[J]. >Journal of Integrative Agriculture, 2024, 23(7): 2458-2475.
[5] Jiangkuan Cui, Haohao Ren, Bo Wang, Fujie Chang, Xuehai Zhang, Haoguang Meng, Shijun Jiang, Jihua Tang.

Hatching and development of maize cyst nematode Heterodera zeae infecting different plant hosts [J]. >Journal of Integrative Agriculture, 2024, 23(5): 1593-1603.

[6] Qilong Song, Jie Zhang, Fangfang Zhang, Yufang Shen, Shanchao Yue, Shiqing Li.

Optimized nitrogen application for maximizing yield and minimizing nitrogen loss in film mulching spring maize production on the Loess Plateau, China [J]. >Journal of Integrative Agriculture, 2024, 23(5): 1671-1684.

[7] Haiqing Gong, Yue Xiang, Jiechen Wu, Laichao Luo, Xiaohui Chen, Xiaoqiang Jiao, Chen Chen.

Integrating phosphorus management and cropping technology for sustainable maize production [J]. >Journal of Integrative Agriculture, 2024, 23(4): 1369-1380.

[8] Pengcheng , Shuangyi Yin, Yunyun Wang, Tianze Zhu, Xinjie Zhu, Minggang Ji, Wenye Rui, Houmiao Wang Chenwu Xu, Zefeng Yang.

Dynamics and genetic regulation of macronutrient concentrations during grain development in maize [J]. >Journal of Integrative Agriculture, 2024, 23(3): 781-794.

[9] Peng Wang, Lan Yang, Xichao Sun, Wenjun Shi, Rui Dong, Yuanhua Wu, Guohua Mi.

Lateral root elongation in maize is related to auxin synthesis and transportation mediated by N metabolism under a mixed NO3 and NH4+ supply [J]. >Journal of Integrative Agriculture, 2024, 23(3): 1048-1060.

[10] Weina Zhang, Zhigan Zhao, Di He, Junhe Liu, Haigang Li, Enli Wang.

Combining field data and modeling to better understand maize growth response to phosphorus (P) fertilizer application and soil P dynamics in calcareous soils [J]. >Journal of Integrative Agriculture, 2024, 23(3): 1006-1021.

[11] Cheng Guo, Xiaojie Zhang, Baobao Wang, Zhihuan Yang, Jiping Li, Shengjun Xu, Chunming Wang, Zhijie Guo, Tianwang Zhou, Liu Hong, Xiaoming Wang, Canxing Duan.

Identification, pathogenicity, and fungicide sensitivity of Eutiarosporella dactylidis associated with leaf blight on maize in China [J]. >Journal of Integrative Agriculture, 2024, 23(3): 888-900.

[12] Binbin Li, Xianmin Chen, Tao Deng, Xue Zhao, Fang Li, Bingchao Zhang, Xin Wang, Si Shen, Shunli Zhou.

Timing effect of high temperature exposure on the plasticity of internode and plant architecture in maize [J]. >Journal of Integrative Agriculture, 2024, 23(2): 551-565.

[13] Minghui Cao, Yan Duan, Minghao Li, Caiguo Tang, Wenjie Kan, Jiangye Li, Huilan Zhang, Wenling Zhong, Lifang Wu.

Manure substitution improves maize yield by promoting soil fertility and mediating the microbial community in lime concretion black soil [J]. >Journal of Integrative Agriculture, 2024, 23(2): 698-710.

[14] Jingui Wei, Qiang Chai, Wen Yin, Hong Fan, Yao Guo, Falong Hu, Zhilong Fan, Qiming Wang. Grain yield and N uptake of maize in response to increased plant density under reduced water and nitrogen supply conditions[J]. >Journal of Integrative Agriculture, 2024, 23(1): 122-140.
[15] YUE Kai, LI Ling-ling, XIE Jun-hong, Zechariah EFFAH, Sumera ANWAR, WANG Lin-lin, MENG Hao-feng, LI Lin-zhi. Integrating microRNAs and mRNAs reveals the hormones synthesis and signal transduction of maize under different N rates[J]. >Journal of Integrative Agriculture, 2023, 22(9): 2673-2686.
No Suggested Reading articles found!