» Articles » PMID: 33879571

An Alternative Resource Allocation Strategy in the Chemolithoautotrophic Archaeon

Overview
Specialty Science
Date 2021 Apr 21
PMID 33879571
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Most microorganisms in nature spend the majority of time in a state of slow or zero growth and slow metabolism under limited energy or nutrient flux rather than growing at maximum rates. Yet, most of our knowledge has been derived from studies on fast-growing bacteria. Here, we systematically characterized the physiology of the methanogenic archaeon during slow growth. was grown in continuous culture under energy (formate)-limiting conditions at different dilution rates ranging from 0.09 to 0.002 h, the latter corresponding to 1% of its maximum growth rate under laboratory conditions (0.23 h). While the specific rate of methanogenesis correlated with growth rate as expected, the fraction of cellular energy used for maintenance increased and the maintenance energy per biomass decreased at slower growth. Notably, proteome allocation between catabolic and anabolic pathways was invariant with growth rate. Unexpectedly, cells maintained their maximum methanogenesis capacity over a wide range of growth rates, except for the lowest rates tested. Cell size, cellular DNA, RNA, and protein content as well as ribosome numbers also were largely invariant with growth rate. A reduced protein synthesis rate during slow growth was achieved by a reduction in ribosome activity rather than via the number of cellular ribosomes. Our data revealed a resource allocation strategy of a methanogenic archaeon during energy limitation that is fundamentally different from commonly studied versatile chemoheterotrophic bacteria such as .

Citing Articles

A framework for understanding collective microbiome metabolism.

Huelsmann M, Schubert O, Ackermann M Nat Microbiol. 2024; 9(12):3097-3109.

PMID: 39604625 DOI: 10.1038/s41564-024-01850-3.


Shaping of microbial phenotypes by trade-offs.

Zhu M, Dai X Nat Commun. 2024; 15(1):4238.

PMID: 38762599 PMC: 11102524. DOI: 10.1038/s41467-024-48591-9.


Improved biological methanation using tubular foam-bed reactor.

Khesali Aghtaei H, Heyer R, Reichl U, Benndorf D Biotechnol Biofuels Bioprod. 2024; 17(1):66.

PMID: 38750538 PMC: 11097517. DOI: 10.1186/s13068-024-02509-1.


Synergistic investigation of natural and synthetic C1-trophic microorganisms to foster a circular carbon economy.

Orsi E, Nikel P, Nielsen L, Donati S Nat Commun. 2023; 14(1):6673.

PMID: 37865689 PMC: 10590403. DOI: 10.1038/s41467-023-42166-w.


In vitro Activity of Cefepime/Avibactam Against Carbapenem Resistant and Integrative Metabolomics-Proteomics Approach for Resistance Mechanism: A Single-Center Study.

Wen L, Luo C, Chen X, Liu T, Li X, Wang M Infect Drug Resist. 2023; 16:6061-6077.

PMID: 37719649 PMC: 10503517. DOI: 10.2147/IDR.S420898.


References
1.
Widdel F, Pfennig N . Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. I. Isolation of new sulfate-reducing bacteria enriched with acetate from saline environments. Description of Desulfobacter postgatei gen. nov., sp. nov. Arch Microbiol. 1981; 129(5):395-400. DOI: 10.1007/BF00406470. View

2.
Cassels R, Oliva B, Knowles D . Occurrence of the regulatory nucleotides ppGpp and pppGpp following induction of the stringent response in staphylococci. J Bacteriol. 1995; 177(17):5161-5. PMC: 177300. DOI: 10.1128/jb.177.17.5161-5165.1995. View

3.
Pirt S . The maintenance energy of bacteria in growing cultures. Proc R Soc Lond B Biol Sci. 1965; 163(991):224-31. DOI: 10.1098/rspb.1965.0069. View

4.
Costa K, Wong P, Wang T, Lie T, Dodsworth J, Swanson I . Protein complexing in a methanogen suggests electron bifurcation and electron delivery from formate to heterodisulfide reductase. Proc Natl Acad Sci U S A. 2010; 107(24):11050-5. PMC: 2890747. DOI: 10.1073/pnas.1003653107. View

5.
Molenaar D, van Berlo R, de Ridder D, Teusink B . Shifts in growth strategies reflect tradeoffs in cellular economics. Mol Syst Biol. 2009; 5:323. PMC: 2795476. DOI: 10.1038/msb.2009.82. View