» Articles » PMID: 32989476

Insights into Growth Kinetics and Roles of Enzymes of Krebs' Cycle and Sulfur Oxidation During Exochemolithoheterotrophic Growth of Achromobacter Aegrifaciens NCCB 38021 on Succinate with Thiosulfate As the Auxiliary Electron Donor

Overview
Journal Arch Microbiol
Specialty Microbiology
Date 2020 Sep 29
PMID 32989476
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Achromobacter aegrifaciens NCCB 38021 was grown heterotrophically on succinate versus exochemolithoheterotrophically on succinate with thiosulfate as auxiliary electron donor. In batch culture, no significant differences in specific molar growth yield or specific growth rate were found for the two growth conditions, but in continuous culture in the succinate-limited chemostat, the maximum specific growth yield coefficient increased by 23.3% with thiosulfate present, consistent with previous studies of endo- and exochemolithoheterotrophs and thermodynamic predictions. Thiosulfate oxidation was coupled to respiration at cytochrome c, and thiosulfate-dependent ATP biosynthesis occurred. Specific activities of cytochrome c-linked thiosulfate dehydrogenase (E.C. 1.8.2.2) and two other enzymes of sulfur metabolism were significantly higher in exochemolithoheterotrophically grown cell extracts, while those of succinyl-transferring 2-oxoglutarate dehydrogenase (E.C. 1.2.4.2), fumarate hydratase (E.C. 4.2.1.2) and malate dehydrogenase (NAD, E.C. 1.1.1.37) were significantly lower-presumably owing to less need to generate reducing equivalents during Krebs' cycle, since they could be produced from thiosulfate oxidation.

Citing Articles

Arsenotrophic Achromobacter aegrifaciens strains isolated from arsenic contaminated tubewell water and soil sources shared similar genomic potentials.

Hoque M, Mannan A, Hossian A, Faisal G, Hossain M, Sultana M BMC Microbiol. 2024; 24(1):518.

PMID: 39627700 PMC: 11616139. DOI: 10.1186/s12866-024-03676-9.


Draft genome sequence of an arsenotrophic strain isolated from soil in Bangladesh.

Hoque M, Hossain A, Faisal G, Bukharid M, Hossain M, Sultana M Microbiol Resour Announc. 2024; 13(11):e0013724.

PMID: 39315834 PMC: 11556063. DOI: 10.1128/mra.00137-24.

References
1.
Boden R . Reclassification of Halothiobacillus hydrothermalis and Halothiobacillus halophilus to Guyparkeria gen. nov. in the Thioalkalibacteraceae fam. nov., with emended descriptions of the genus Halothiobacillus and family Halothiobacillaceae. Int J Syst Evol Microbiol. 2017; 67(10):3919-3928. DOI: 10.1099/ijsem.0.002222. View

2.
Boden R, Murrell J . Response to mercury (II) ions in Methylococcus capsulatus (Bath). FEMS Microbiol Lett. 2011; 324(2):106-10. DOI: 10.1111/j.1574-6968.2011.02395.x. View

3.
Boden R, Scott K . Evaluation of the genus Thiothrix Winogradsky 1888 (Approved Lists 1980) emend. Aruga et al. 2002: reclassification of Thiothrix disciformis to Thiolinea disciformis gen. nov., comb. nov., and of Thiothrix flexilis to Thiofilum flexile gen. nov.,.... Int J Syst Evol Microbiol. 2018; 68(7):2226-2239. DOI: 10.1099/ijsem.0.002816. View

4.
Boden R, Murrell J, Schafer H . Dimethylsulfide is an energy source for the heterotrophic marine bacterium Sagittula stellata. FEMS Microbiol Lett. 2011; 322(2):188-93. DOI: 10.1111/j.1574-6968.2011.02349.x. View

5.
Boden R, Cleland D, Green P, Katayama Y, Uchino Y, Murrell J . Phylogenetic assessment of culture collection strains of Thiobacillus thioparus, and definitive 16S rRNA gene sequences for T. thioparus, T. denitrificans, and Halothiobacillus neapolitanus. Arch Microbiol. 2011; 194(3):187-95. DOI: 10.1007/s00203-011-0747-0. View