» Articles » PMID: 1518815

Multicellular Oxidant Defense in Unicellular Organisms

Overview
Specialty Science
Date 1992 Sep 1
PMID 1518815
Citations 48
Authors
Affiliations
Soon will be listed here.
Abstract

Although catalase is thought to be a major defense against hydrogen peroxide (H2O2), the catalase activity within individual Escherichia coli fails to protect against exogenous H2O2. Contrary to earlier reports, we find that dilute suspensions of wild-type and catalase-deficient E. coli are identical in their sensitivity to H2O2, perhaps because even wild-type, catalase-positive E. coli cannot maintain an internal/external concentration gradient of this highly diffusible oxidant. However, concentrated suspensions or colonies of catalase-positive E. coli do preferentially survive H2O2 challenge and can even cross-protect adjacent catalase-deficient organisms. Furthermore, high-density catalase-positive--but not catalase-negative--E. coli can survive and multiply in the presence of competitive, peroxide-generating streptococci. These observations support the concept that bacterial catalase may defend colonial, but not individual, E. coli against environmental H2O2. Group protection by the activity of enzymes that mitigate oxidative stress may have been a driving force in the evolution of multicellular organisms.

Citing Articles

Collective peroxide detoxification determines microbial mutation rate plasticity in E. coli.

Green R, Wang H, Botchey C, Zhang S, Wadsworth C, Tyrrell F PLoS Biol. 2024; 22(7):e3002711.

PMID: 39008532 PMC: 11272383. DOI: 10.1371/journal.pbio.3002711.


Modeling the reactive oxygen species (ROS) wave in Chlamydomonas reinhardtii colonies.

Zhou Y, Fichman Y, Zhang S, Mittler R, Chen S Free Radic Biol Med. 2024; 222:165-172.

PMID: 38851517 PMC: 11344667. DOI: 10.1016/j.freeradbiomed.2024.06.003.


Chaos in a bacterial stress response.

Choudhary D, Foster K, Uphoff S Curr Biol. 2023; 33(24):5404-5414.e9.

PMID: 38029757 PMC: 7616676. DOI: 10.1016/j.cub.2023.11.002.


Phenotypic heterogeneity in the bacterial oxidative stress response is driven by cell-cell interactions.

Choudhary D, Lagage V, Foster K, Uphoff S Cell Rep. 2023; 42(3):112168.

PMID: 36848288 PMC: 10935545. DOI: 10.1016/j.celrep.2023.112168.


Physiological roles of catalases Cat1 and Cat2 in Myxococcus xanthus.

Yoshio K, Yoshioka Y, Toshikuni K J Microbiol. 2022; 60(12):1168-1177.

PMID: 36279102 DOI: 10.1007/s12275-022-2277-7.


References
1.
Hillman J, Shivers M . Interaction between wild-type, mutant and revertant forms of the bacterium Streptococcus sanguis and the bacterium Actinobacillus actinomycetemcomitans in vitro and in the gnotobiotic rat. Arch Oral Biol. 1988; 33(6):395-401. DOI: 10.1016/0003-9969(88)90196-3. View

2.
Cooper W, Zika R . Photochemical formation of hydrogen peroxide in surface and ground waters exposed to sunlight. Science. 1983; 220(4598):711-2. DOI: 10.1126/science.220.4598.711. View

3.
Imlay J, Linn S . Mutagenesis and stress responses induced in Escherichia coli by hydrogen peroxide. J Bacteriol. 1987; 169(7):2967-76. PMC: 212335. DOI: 10.1128/jb.169.7.2967-2976.1987. View

4.
Carlsson J, Edlund M, Lundmark S . Characteristics of a hydrogen peroxide-forming pyruvate oxidase from Streptococcus sanguis. Oral Microbiol Immunol. 1987; 2(1):15-20. DOI: 10.1111/j.1399-302x.1987.tb00264.x. View

5.
Greenberg J, Demple B . Glutathione in Escherichia coli is dispensable for resistance to H2O2 and gamma radiation. J Bacteriol. 1986; 168(2):1026-9. PMC: 213589. DOI: 10.1128/jb.168.2.1026-1029.1986. View