» Articles » PMID: 18430135

The Global, PpGpp-mediated Stringent Response to Amino Acid Starvation in Escherichia Coli

Overview
Journal Mol Microbiol
Date 2008 Apr 24
PMID 18430135
Citations 290
Authors
Affiliations
Soon will be listed here.
Abstract

The stringent response to amino acid starvation, whereby stable RNA synthesis is curtailed in favour of transcription of amino acid biosynthetic genes, is controlled by the alarmone ppGpp. To elucidate the extent of gene expression effected by ppGpp, we designed an experimental system based on starvation for isoleucine, which could be applied to both wild-type Escherichia coli and the multiauxotrophic relA spoT mutant (ppGpp(0)). We used microarrays to profile the response to amino acid starvation in both strains. The wild-type response included induction of the general stress response, downregulation of genes involved in production of macromolecular structures and comprehensive restructuring of metabolic gene expression, but not induction of amino acid biosynthesis genes en masse. This restructuring of metabolism was confirmed using kinetic Biolog assays. These responses were profoundly altered in the ppGpp(0) strain. Furthermore, upon isoleucine starvation, the ppGpp(0) strain exhibited a larger cell size and continued growth, ultimately producing 50% more biomass than the wild-type, despite producing a similar amount of protein. This mutant phenotype correlated with aberrant gene expression in diverse processes, including DNA replication, cell division, and fatty acid and membrane biosynthesis. We present a model that expands and functionally integrates the ppGpp-mediated stringent response to include control of virtually all macromolecular synthesis and intermediary metabolism.

Citing Articles

Cell size regulation in bacteria: a tale of old regulators with new mechanisms.

Khan E, Mera P bioRxiv. 2025; .

PMID: 40027726 PMC: 11870628. DOI: 10.1101/2025.02.22.639668.


Toxin-antitoxin genes are differentially expressed in and mutans cultured under nitrogen, fatty acid, or carbon starvation conditions.

Maciag-Dorszynska M, Olszewski P, Karczewska M, Boss L Front Microbiol. 2025; 15:1528825.

PMID: 39895937 PMC: 11783221. DOI: 10.3389/fmicb.2024.1528825.


Effect of Light Regime on Puniceispirillum marinum IMCC1322 in Nutrient-Replete Conditions.

Oh H, Lee J, Choi A, Yang S, Shin G, Kang S J Microbiol Biotechnol. 2025; 35:e2410034.

PMID: 39809517 PMC: 11813361. DOI: 10.4014/jmb.2410.10034.


Molecular mechanism and application of emerging technologies in study of bacterial persisters.

Yuan S, Shen Y, Quan Y, Gao S, Zuo J, Jin W BMC Microbiol. 2024; 24(1):480.

PMID: 39548389 PMC: 11568608. DOI: 10.1186/s12866-024-03628-3.


Gut microbiota-derived butyrate selectively interferes with growth of carbapenem-resistant based on their resistance mechanism.

Happ E, Schulze K, Afrin Z, Woltemate S, Gorner P, Ziesing S Gut Microbes. 2024; 16(1):2397058.

PMID: 39292563 PMC: 11529417. DOI: 10.1080/19490976.2024.2397058.


References
1.
Taguchi M, Izui K, Katsuki H . Augmentation of glycogen synthesis under stringent control in Escherichia coli. J Biochem. 1980; 88(2):379-87. DOI: 10.1093/oxfordjournals.jbchem.a132983. View

2.
Stent G, Brenner S . A genetic locus for the regulation of ribonucleic acid synthesis. Proc Natl Acad Sci U S A. 1961; 47:2005-14. PMC: 223254. DOI: 10.1073/pnas.47.12.2005. View

3.
Schreiber G, Ron E, Glaser G . ppGpp-mediated regulation of DNA replication and cell division in Escherichia coli. Curr Microbiol. 1995; 30(1):27-32. DOI: 10.1007/BF00294520. View

4.
Wren J, Conway T . Meta-analysis of published transcriptional and translational fold changes reveals a preference for low-fold inductions. OMICS. 2006; 10(1):15-27. DOI: 10.1089/omi.2006.10.15. View

5.
Tosa T, PIZER L . Biochemical bases for the antimetabolite action of L-serine hydroxamate. J Bacteriol. 1971; 106(3):972-82. PMC: 248741. DOI: 10.1128/jb.106.3.972-982.1971. View