Plant Physiol. Journal of Pharmacology and Experimental Therapeutics
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First published online January 19, 2007; 10.1104/pp.106.091736

Plant Physiology 143:1385-1397 (2007)
© 2007 American Society of Plant Biologists

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SYSTEMS BIOLOGY, MOLECULAR BIOLOGY, AND GENE REGULATION

Carbon Cycling in Anabaena sp. PCC 7120. Sucrose Synthesis in the Heterocysts and Possible Role in Nitrogen Fixation1,[OA]

Andrea C. Cumino, Clarisa Marcozzi, Roberto Barreiro2 and Graciela L. Salerno*

Centro de Investigaciones Biológicas, Fundación para Investigaciones Biológicas Aplicadas, 7600 Mar del Plata, Argentina

Nitrogen (N) available to plants mostly originates from N2 fixation carried out by prokaryotes. Certain cyanobacterial species contribute to this energetically expensive process related to carbon (C) metabolism. Several filamentous strains differentiate heterocysts, specialized N2-fixing cells. To understand how C and N metabolism are regulated in photodiazotrophically grown organisms, we investigated the role of sucrose (Suc) biosynthesis in N2 fixation in Anabaena sp. PCC 7120 (also known as Nostoc sp. PCC 7120). The presence of two Suc-phosphate synthases (SPS), SPS-A and SPS-B, directly involved in Suc synthesis with different glucosyl donor specificity, seems to be important in the N2-fixing filament. Measurement of enzyme activity and polypeptide levels plus reverse transcription-polymerase chain reaction experiments showed that total SPS expression is greater in cells grown in N2 versus combined N conditions. Only SPS-B, however, was seen to be active in the heterocyst, as confirmed by analysis of green fluorescent protein reporters. SPS-B gene expression is likely controlled at the transcriptional initiation level, probably in relation to a global N regulator. Metabolic control analysis indicated that the metabolism of glycogen and Suc is likely interconnected in N2-fixing filaments. These findings suggest that N2 fixation may be spatially compatible with Suc synthesis and support the role of the disaccharide as an intermediate in the reduced C flux in heterocyst-forming cyanobacteria.


1 This work was supported by the Agencia Nacional de Promoción Científica y Tecnológica, Consejo Nacional de Investigaciones Científicas y Tecnológicas, Fundación para Investigaciones Biológicas Aplicadas, and Universidad Nacional de Mar del Plata, Argentina.

2 Present address: Pioneer Hi-Bred International (a DuPont company), 7300 N.W. 62nd Ave., Johnston, IA 50131.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Graciela L. Salerno (gsalerno{at}fiba.org.ar).

[OA] Open Access articles can be viewed online without a subscription.

www.plantphysiol.org/cgi/doi/10.1104/pp.106.091736

* Corresponding author; e-mail gsalerno{at}fiba.org.ar; fax 54–223–475–7120.

Received October 21, 2006; accepted January 8, 2006; published January 19, 2007.







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