Plastid-expressed betaine aldehyde dehydrogenase gene in carrot cultured cells, roots, and leaves confers enhanced salt tolerance

被引:234
作者
Kumar, S [1 ]
Dhingra, A [1 ]
Daniell, H [1 ]
机构
[1] Univ Cent Florida, Dept Mol Biol & Microbiol, Orlando, FL 32816 USA
关键词
D O I
10.1104/pp.104.045187
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Salinity is one of the major factors that limits geographical distribution of plants and adversely affects crop productivity and quality. We report here high-level expression of betaine aldehyde dehydrogenase (BADH) in cultured cells, roots, and leaves of carrot (Daucus carota) via plastid genetic engineering. Homoplasmic transgenic plants exhibiting high levels of salt tolerance were regenerated from bombarded cell cultures via somatic embryogenesis. Transformation efficiency of carrot somatic embryos was very high, with one transgenic event per approximately seven bombarded plates under optimal conditions. In vitro transgenic carrot cells transformed with the badh transgene were visually green in color when compared to untransformed carrot cells, and this offered a visual selection for transgenic lines. BADH enzyme activity was enhanced 8-fold in transgenic carrot cell cultures, grew 7-fold more, and accumulated 50- to 54-fold more betaine (93-101 mumol g(-1) dry weight of beta-Ala betaine and Gly betaine) than untransformed cells grown in liquid medium containing 100 mM NaCl. Transgenic carrot plants expressing BADH grew in the presence of high concentrations of NaCl (up to 400 mM), the highest level of salt tolerance reported so far among genetically modified crop plants. BADH expression was 74.8% in non-green edible parts (carrots) containing chromoplasts, and 53% in proplastids of cultured cells when compared to chloroplasts (100%) in leaves. Demonstration of plastid transformation via somatic embryogenesis utilizing non-green tissues as recipients of foreign DNA for the first time overcomes two of the major obstacles in extending this technology to important crop plants.
引用
收藏
页码:2843 / 2854
页数:12
相关论文
共 76 条
[1]   Enhanced tolerance to light stress of transgenic Arabidopsis plants that express the codA gene for a bacterial choline oxidase [J].
Alia ;
Kondo, Y ;
Sakamoto, A ;
Nonaka, H ;
Hayashi, H ;
Saradhi, PP ;
Chen, THH ;
Murata, N .
PLANT MOLECULAR BIOLOGY, 1999, 40 (02) :279-288
[2]   PHOTOINHIBITION OF PHOTOSYSTEM-2 - INACTIVATION, PROTEIN DAMAGE AND TURNOVER [J].
ARO, EM ;
VIRGIN, I ;
ANDERSSON, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1143 (02) :113-134
[3]   A single-stop purification for glycine betaine determination in plant extracts by isocratic HPLC [J].
Bessieres, MA ;
Gibon, Y ;
Lefeuvre, JC ;
Larher, F .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (09) :3718-3722
[4]   Engineering chloroplasts: an alternative site for foreign genes, proteins, reactions and products [J].
Bogorad, L .
TRENDS IN BIOTECHNOLOGY, 2000, 18 (06) :257-263
[5]   Genomic approaches to plant stress tolerance [J].
Cushman, JC ;
Bohnert, HJ .
CURRENT OPINION IN PLANT BIOLOGY, 2000, 3 (02) :117-124
[6]  
Daniell H, 2005, METH MOL B, V286, P111
[7]   Expression of the native cholera toxin B subunit gene and assembly as functional oligomers in transgenic tobacco chloroplasts [J].
Daniell, H ;
Lee, SB ;
Panchal, T ;
Wiebe, PO .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 311 (05) :1001-1009
[8]   Molecular strategies for gene containment in transgenic crops [J].
Daniell, H .
NATURE BIOTECHNOLOGY, 2002, 20 (06) :581-586
[9]   Marker tree transgenic plants: engineering the chloroplast genome without the use of antibiotic selection [J].
Daniell, H ;
Muthukumar, B ;
Lee, SB .
CURRENT GENETICS, 2001, 39 (02) :109-116
[10]   Milestones in chloroplast genetic engineering: an environmentally friendly era in biotechnology [J].
Daniell, H ;
Khan, MS ;
Allison, L .
TRENDS IN PLANT SCIENCE, 2002, 7 (02) :84-91