Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Koyama, H.
Right arrow Articles by Shibata, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Koyama, H.
Right arrow Articles by Shibata, D.
Agricola
Right arrow Articles by Koyama, H.
Right arrow Articles by Shibata, D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Plant and Cell Physiology, 1999, Vol. 40, No. 5 482-488
© 1999

Over Expression of Mitochondrial Citrate Synthase Gene Improves the Growth of Carrot Cells in Al-Phosphate Medium

Hiroyuki Koyama1,3, Eiji Takita1, Ayako Kawamura1, Tetsuo Hara1 and Daisuke Shibata2

1 Laboratory of Plant Cell Technology, Faculty of Agriculture, Gifu University 1-1 Yanagido, Gifu, 501-1193 Japan
2 Mitsui Plant Biotechnology Research Institute Sengen 2-1-6, TCI-D21, Tsukuba, Ibaraki, 305-0047 Japan

3To whom correspondence should be addressed, e-mail, koyama{at}cc.gifu-u.ac.jp

A mitochondrial citrate synthase (CS) of Arabidopsis thaliana was introduced into carrot (Daucus carota L. cv. MS Yonsun) cells by Agrobacterium tumefaciens-mediated transformation. Transgenic cell lines had high CS activity, the highest value observed was 0.24µmol (mg protein)–1 min–1 which was 1.9-fold of that in wild-type cells. Transcript levels of DcCS were similar between transgenic lines, but those of AtCS were increased as the CS activity of cells was increased. Isoelectric focussing revealed that the CS polypeptide of the transgenic lines had a pI value different from that of the wild-type cells, although the molecular mass was the same. These results indicate that the CS polypeptides of A. thaliana were expressed and processed to the mature form in carrot cells. The growth rate and excretion was 2.2–2.8 and 2.8–4.0 fold greater in the transgenic cells than in the wild type cells, respectively. Phosphate uptake from Al-phosphate also increased in transgenic cells. It appeares, the overexpression of mitochondrial citrate synthase in carrot cells improves the growth rate in Al-phosphate medium possibly as a result of increased citrate excretion.

(Received August 27, 1998; Accepted February 21, 1999)
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Plant Physiol.Home page
Y. Sawaki, S. Iuchi, Y. Kobayashi, Y. Kobayashi, T. Ikka, N. Sakurai, M. Fujita, K. Shinozaki, D. Shibata, M. Kobayashi, et al.
STOP1 Regulates Multiple Genes That Protect Arabidopsis from Proton and Aluminum Toxicities
Plant Physiology, May 1, 2009; 150(1): 281 - 294.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
T. Kihara, T. Wada, Y. Suzuki, T. Hara, and H. Koyama
Alteration of Citrate Metabolism in Cluster Roots of White Lupin
Plant Cell Physiol., September 15, 2003; 44(9): 901 - 908.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
V. M. Anoop, U. Basu, M. T. McCammon, L. McAlister-Henn, and G. J. Taylor
Modulation of Citrate Metabolism Alters Aluminum Tolerance in Yeast and Transgenic Canola Overexpressing a Mitochondrial Citrate Synthase
Plant Physiology, August 1, 2003; 132(4): 2205 - 2217.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
S. Takahashi, N. Nakajima, H. Saji, and N. Kondo
Diurnal Change of Cucumber CPD Photolyase Gene (CsPHR) Expression and Its Physiological Role in Growth under UV-B Irradiation
Plant Cell Physiol., March 1, 2002; 43(3): 342 - 349.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
C. P. Vance
Symbiotic Nitrogen Fixation and Phosphorus Acquisition. Plant Nutrition in a World of Declining Renewable Resources
Plant Physiology, October 1, 2001; 127(2): 390 - 397.
[Full Text] [PDF]


Home page
Plant Physiol.Home page
M. Kollmeier, P. Dietrich, C. S. Bauer, W. J. Horst, and R. Hedrich
Aluminum Activates a Citrate-Permeable Anion Channel in the Aluminum-Sensitive Zone of the Maize Root Apex. A Comparison Between an Aluminum- Sensitive and an Aluminum-Resistant Cultivar
Plant Physiology, May 1, 2001; 126(1): 397 - 410.
[Abstract] [Full Text]


Home page
Plant Physiol.Home page
E. Delhaize, D. M. Hebb, and P. R. Ryan
Expression of a Pseudomonas aeruginosa Citrate Synthase Gene in Tobacco Is Not Associated with Either Enhanced Citrate Accumulation or Efflux
Plant Physiology, April 1, 2001; 125(4): 2059 - 2067.
[Abstract] [Full Text]


Home page
Plant Physiol.Home page
P. Wenzl, G. M. Patiño, A. L. Chaves, J. E. Mayer, and I. M. Rao
The High Level of Aluminum Resistance in Signalgrass Is Not Associated with Known Mechanisms of External Aluminum Detoxification in Root Apices
Plant Physiology, March 1, 2001; 125(3): 1473 - 1484.
[Abstract] [Full Text]


Home page
Plant Cell PhysiolHome page
H. Koyama, A. Kawamura, T. Kihara, T. Hara, E. Takita, and D. Shibata
Overexpression of Mitochondrial Citrate Synthase in Arabidopsis thaliana Improved Growth on a Phosphorus-Limited Soil
Plant Cell Physiol., September 1, 2000; 41(9): 1030 - 1037.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
X. F. Li, J. F. Ma, and H. Matsumoto
Pattern of Aluminum-Induced Secretion of Organic Acids Differs between Rye and Wheat
Plant Physiology, August 1, 2000; 123(4): 1537 - 1544.
[Abstract] [Full Text]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.