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Proteome changes driven by phosphorus deficiency and recovery in the brown tide-forming alga Aureococcus anophagefferens
Authors
A Keller
AA Keller
+73 more
AE Allen
AJ Saldanha
B Essigmann
B Palenik
B Zhang
BAS Van Mooy
Benjamin A. S. Van Mooy
BL Nunn
BM Jones
BMF Pearse
C Fan
CC Chung
CJ Gobler
CJ Gobler
CJ Gobler
CJ Gobler
CJ Gobler
DI Greenfield
DI Greenfield
DN Wilson
E Birney
Erin M. Bertrand
FM Brodsky
G Ballihaut
GM Berg
GM Berg
H Nielsen
H-Y Kim
J LaRoche
JD Bendtsen
JF Hare
JW Ammerman
KJ Flynn
KJ Livak
KJ Popendorf
L Kall
LL Wurch
Louie L. Wurch
M Kato
M Malamy
M Nagano
M Zuker
MA Saito
Mak A. Saito
MB Eisen
ME Theodorou
ML Fournier
MR Mulholland
MS Parker
MV Lee
MW Pfaffl
NA Kamennaya
NA Kamennaya
P Martin
RM Morris
RRL Guillard
S Ma
SD Conner
SM Sowell
Sonya T. Dyhrman
ST Dyhrman
ST Dyhrman
ST Dyhrman
ST Dyhrman
T Kirchhausen
T Le Bihan
Terence Evens
TM Kana
WC Dennison
WC Paxton
WG Sunda
WR Riekhof
XN Lu
Publication date
1 January 2011
Publisher
'Public Library of Science (PLoS)'
Doi
View
on
PubMed
Abstract
© The Author(s), 2011. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in PLoS One 6 (2011): e28949, doi:10.1371/journal.pone.0028949.Shotgun mass spectrometry was used to detect proteins in the harmful alga, Aureococcus anophagefferens, and monitor their relative abundance across nutrient replete (control), phosphate-deficient (−P) and −P refed with phosphate (P-refed) conditions. Spectral counting techniques identified differentially abundant proteins and demonstrated that under phosphate deficiency, A. anophagefferens increases proteins involved in both inorganic and organic phosphorus (P) scavenging, including a phosphate transporter, 5′-nucleotidase, and alkaline phosphatase. Additionally, an increase in abundance of a sulfolipid biosynthesis protein was detected in −P and P-refed conditions. Analysis of the polar membrane lipids showed that cellular concentrations of the sulfolipid sulphoquinovosyldiacylglycerol (SQDG) were nearly two-fold greater in the −P condition versus the control condition, while cellular phospholipids were approximately 8-fold less. Transcript and protein abundances were more tightly coupled for gene products involved in P metabolism compared to those involved in a range of other metabolic functions. Comparison of protein abundances between the −P and P-refed conditions identified differences in the timing of protein degradation and turnover. This suggests that culture studies examining nutrient starvation responses will be valuable in interpreting protein abundance patterns for cellular nutritional status and history in metaproteomic datasets.Research for this work was supported by a National Oceanic and Atmospheric Administration ECOHAB grant (#NA09NOS4780206) and National Science Foundation grant (#OCE-0723667) and a STAR Research Assistance Agreement No. R-83041501-0 awarded by the U.S. Environmental Protection Agency. Further support came from the Woods Hole Coastal Ocean Institute. LLW was supported by a Environmental Protection Agency STAR Fellowship (#FP916901). EMB was supported by a National Science Foundation (NSF) Graduate Research Fellowship (#2007037200) and an Environmental Protection Agency STAR Fellowship (#F6E20324)
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