Increased sucrose level and altered nitrogen metabolism in Arabidopsis thaliana transgenic plants expressing antisense chloroplastic fructose-1,6-bisphosphatase

J Exp Bot. 2004 Dec;55(408):2495-503. doi: 10.1093/jxb/erh257. Epub 2004 Sep 24.

Abstract

The pea chloroplastic fructose-1,6-bisphosphatase (FBPase) antisense construct reduced the endogenous level of expression of the corresponding Arabidopsis thaliana gene. The reduction of foliar FBPase activity in the transformants T(2) and T(3) generation ranged from 20% to 42%, and correlated with lower levels of FBPase protein. FBPase antisense plants displayed different phenotypes with a clear increase in leaf fresh weight. Measurements of photosynthesis revealed a higher carbon-assimilation rate. Decreased FBPase activity boosted the foliar carbohydrate contents, with a shift in the sucrose:starch ratio, which reached a maximum of 0.99 when the activity loss was 41%. Nitrate reductase activity decreased simultaneously with an increase in glutamine synthetase activity, which could be explained in terms of ammonium assimilation regulation by sugar content. These results suggest the role of FBPase as a key enzyme in CO(2) assimilation, and also in co-ordinating carbon and nitrogen metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antisense Elements (Genetics) / genetics
  • Antisense Elements (Genetics) / metabolism
  • Arabidopsis / genetics
  • Arabidopsis / metabolism*
  • Carbohydrate Metabolism
  • Chloroplasts / enzymology
  • Fructose-Bisphosphatase / genetics
  • Fructose-Bisphosphatase / metabolism*
  • Glutamate-Ammonia Ligase / metabolism
  • Nitrate Reductase
  • Nitrate Reductases / metabolism
  • Nitrogen / metabolism*
  • Phenotype
  • Pisum sativum / enzymology
  • Pisum sativum / genetics
  • Plant Leaves / anatomy & histology
  • Plants, Genetically Modified
  • Sucrose / metabolism*

Substances

  • Antisense Elements (Genetics)
  • Sucrose
  • Nitrate Reductases
  • Nitrate Reductase
  • Fructose-Bisphosphatase
  • Glutamate-Ammonia Ligase
  • Nitrogen