Plant Physiol. Drug Metab Dispos
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
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 Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Web of Science (16)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Takahashi, H.
Right arrow Articles by Grossman, A. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Takahashi, H.
Right arrow Articles by Grossman, A. R.
Agricola
Right arrow Articles by Takahashi, H.
Right arrow Articles by Grossman, A. R.

Plant Physiol, October 2001, Vol. 127, pp. 665-673

Sulfur Economy and Cell Wall Biosynthesis during Sulfur Limitation of Chlamydomonas reinhardtii1

Hideki Takahashi, Caren E. Braby, and Arthur R. Grossman*

The Institute of Physical and Chemical Research Plant Science Center, Hirosawa 2-1, Wako, Saitama 351-0198, Japan (H.T.); Stanford University, Department of Biology, The Hopkins Marine Station, Oceanview Boulevard, Pacific Grove, California 93950-3094 (C.E.B.); and Department of Plant Biology, The Carnegie Institution of Washington, 260 Panama Street, Stanford, California 94305 (A.R.G.)

We have identified two novel periplasmic/cell wall polypeptides that specifically accumulate during sulfur limitation of Chlamydomonas reinhardtii. These polypeptides, present at high levels in the extracellular polypeptide fraction from a sulfur-deprived, cell wall-minus C. reinhardtii strain, have apparent molecular masses of 76 and 88 kD and are designated Ecp76 and Ecp88. N-terminal sequences of these polypeptides facilitated the isolation of full-length Ecp76 and Ecp88 cDNAs. Ecp76 and Ecp88 polypeptides are deduced to be 583 and 595 amino acids, respectively. Their amino acid sequences are similar to each other, with features characteristic of cell wall-localized hydroxyproline-rich glycoproteins; the N terminus of each polypeptide contains a predicted signal sequence, whereas the C terminus is rich in proline, alanine, and serine. Ecp76 and Ecp88 have either no (Ecp88) or one (Ecp76) sulfur-containing amino acid and transcripts encoding these polypeptides are not detected in cultures maintained on complete medium, but accumulate when cells are deprived of sulfur. This accumulation is temporally delayed relative to the accumulation of sulfur stress-induced arylsulfatase and ATP sulfurylase transcripts. The addition of sulfate back to sulfur-starved cultures caused a rapid decline in Ecp76 and Ecp88 mRNAs (half lives < 10 min). Furthermore, the C. reinhardtii sac1 mutant, which lacks a regulatory protein critical for acclimation to sulfur limitation, does not accumulate Ecp76 or Ecp88 transcripts. These results suggest that the Ecp76 and Ecp88 genes are under SacI control, and that restructuring of the C. reinhardtii cell wall during sulfur limitation may be important for redistribution of internal and efficient utilization of environmental sulfur-containing molecules.


1 This work was supported by the Japan Society for the Promotion of Science (postdoctoral fellowship no. 6067 to H.T.). This work was supported in part by the U.S. Department of Agriculture (grant no. 9900622 awarded to J. Davies [Exelixis Pharmaceuticals, San Francisco] and transferred to A.R.G.). This is Carnegie Institution Publication No. 1486.

* Corresponding author; e-mail arthur{at}andrew2.stanford.edu; fax 650-325-6857.

© 2001 American Society of Plant Physiologists



This article has been cited by other articles:


Home page
Eukaryot CellHome page
A. V. Nguyen, S. R. Thomas-Hall, A. Malnoe, M. Timmins, J. H. Mussgnug, J. Rupprecht, O. Kruse, B. Hankamer, and P. M. Schenk
Transcriptome for Photobiological Hydrogen Production Induced by Sulfur Deprivation in the Green Alga Chlamydomonas reinhardtii
Eukaryot. Cell, November 1, 2008; 7(11): 1965 - 1979.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
D. Gonzalez-Ballester, S. V. Pollock, W. Pootakham, and A. R. Grossman
The Central Role of a SNRK2 Kinase in Sulfur Deprivation Responses
Plant Physiology, May 1, 2008; 147(1): 216 - 227.
[Abstract] [Full Text] [PDF]


Home page
ANN BOT (LOND)Home page
S. KOPRIVA
Regulation of Sulfate Assimilation in Arabidopsis and Beyond
Ann. Bot., April 1, 2006; 97(4): 479 - 495.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
C. Bolling and O. Fiehn
Metabolite Profiling of Chlamydomonas reinhardtii under Nutrient Deprivation
Plant Physiology, December 1, 2005; 139(4): 1995 - 2005.
[Abstract] [Full Text] [PDF]


Home page
Eukaryot CellHome page
Z. Zhang, J. Shrager, M. Jain, C.-W. Chang, O. Vallon, and A. R. Grossman
Insights into the Survival of Chlamydomonas reinhardtii during Sulfur Starvation Based on Microarray Analysis of Gene Expression
Eukaryot. Cell, October 1, 2004; 3(5): 1331 - 1348.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
S. Kopriva and H. Rennenberg
Control of sulphate assimilation and glutathione synthesis: interaction with N and C metabolism
J. Exp. Bot., August 1, 2004; 55(404): 1831 - 1842.
[Abstract] [Full Text] [PDF]


Home page
Eukaryot CellHome page
A. R. Grossman, E. E. Harris, C. Hauser, P. A. Lefebvre, D. Martinez, D. Rokhsar, J. Shrager, C. D. Silflow, D. Stern, O. Vallon, et al.
Chlamydomonas reinhardtii at the Crossroads of Genomics
Eukaryot. Cell, December 1, 2003; 2(6): 1137 - 1150.
[Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
S. Kosourov, M. Seibert, and M. L. Ghirardi
Effects of Extracellular pH on the Metabolic Pathways in Sulfur-Deprived, H2-Producing Chlamydomonas reinhardtii Cultures
Plant Cell Physiol., February 15, 2003; 44(2): 146 - 155.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
J. Shrager, C. Hauser, C.-W. Chang, E. H. Harris, J. Davies, J. McDermott, R. Tamse, Z. Zhang, and A. R. Grossman
Chlamydomonas reinhardtii Genome Project. A Guide to the Generation and Use of the cDNA Information
Plant Physiology, February 1, 2003; 131(2): 401 - 408.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
C. G. Ravina, C.-I. Chang, G. P. Tsakraklides, J. P. McDermott, J. M. Vega, T. Leustek, C. Gotor, and J. P. Davies
The sac Mutants of Chlamydomonas reinhardtii Reveal Transcriptional and Posttranscriptional Control of Cysteine Biosynthesis
Plant Physiology, December 1, 2002; 130(4): 2076 - 2084.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 2001 by the American Society of Plant Biologists