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 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 Nomsawai, P.
Right arrow Articles by Cheevadhanarak, S.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Nomsawai, P.
Right arrow Articles by Cheevadhanarak, S.
Agricola
Right arrow Articles by Nomsawai, P.
Right arrow Articles by Cheevadhanarak, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Plant and Cell Physiology, 1999, Vol. 40, No. 12 1194-1202
© 1999

Light Regulation of Phycobilisome Structure and Gene Expression in Spirulina platensis C1 (Arthrospira sp. PCC 9438)

Pinthipya Nomsawai1,2,3, Nicole Tandeau de Marsac2, Jean Claude Thomas3, Morakot Tanticharoen1,4 and Supapon Cheevadhanarak1

1 School of Bioresources and Technology, King Mongkut's University of Technology Thonburi Bangkok 10140, Thailand
2 Unité de Physiologie Microbienne, Institut Pasteur 75724 Paris Cedex 15, France
3 Laboratoire de Photorégulation et Dynamique des Membranes Végétales, CNRS URA 1810, Ecole Normale Supérieure Paris Cedex 05, France
4 National Center for Genetic Engineering and Biotechnology Bangkok 10400, Thailand

Light intensity is the most significant environmental factor influencing the light harvesting complexes (phycobilisomes) in cyanobacteria. Spirulina platensis C1, a filamentous cyanobacterium, was grown in batch culture under low (50 µE m–2s–1) and high (500 µE m–2s–1) photosynthetic photon flux density. Phycobilisomes were isolated, purified and analyzed by spectrophotometry, gel electrophoresis and electron microscopy. The absorption spectra in conjunction with the electron micrographs revealed that they are hemidiscoidal with three allophycocyanin cylindrical cores and six phycocyanin rods radiating from the core. The 33 kDa linker polypeptide normally found in low light cells disappeared under high light resulting in smaller phycobilisomes. The decrease in the number of phycobilisomes correlated well with the decrease in phycocyanin and allophycocyanin content from cells shifted from low to high light. The phycobiliprotein transcripts exhibited different pattern in response to different light intensities. Three species of phycocyanin mRNA of sizes 1.4, 1.5 and 3.5 kb and two species of allophycocyanin of 1.4 and 1.7 kb were found in low light grown cells. However in high light, the 3.5 kb phycocyanin transcript disappeared while the others remained with subtle changes. This observation indicates that the largest transcript encoding for phycocyanin subunits and linker polypeptides and the phycobilisome structure are modulated by light intensity.

(Received January 21, 1999; Accepted October 12, 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
J. Bacteriol.Home page
C. Six, J.-C. Thomas, L. Thion, Y. Lemoine, F. Zal, and F. Partensky
Two Novel Phycoerythrin-Associated Linker Proteins in the Marine Cyanobacterium Synechococcus sp. Strain WH8102
J. Bacteriol., March 1, 2005; 187(5): 1685 - 1694.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
E. Miskiewicz, A. G. Ivanov, and N. P.A. Huner
Stoichiometry of the Photosynthetic Apparatus and Phycobilisome Structure of the Cyanobacterium Plectonema boryanum UTEX 485 Are Regulated by Both Light and Temperature
Plant Physiology, November 1, 2002; 130(3): 1414 - 1425.
[Abstract] [Full Text] [PDF]



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.