Hydrogen sulfide-producing kinetics of Shewanella oneidensis in sulfite and thiosulfate respiration

2020 ◽  
Vol 93 ◽  
pp. 21-27
Author(s):  
Wu Genfu
AIChE Journal ◽  
1984 ◽  
Vol 30 (6) ◽  
pp. 1021-1025 ◽  
Author(s):  
Pan Zhenglu ◽  
Hung-Shan Weng ◽  
Feng Han-Yu ◽  
J. M. Smith

2008 ◽  
Vol 394 (1) ◽  
pp. 162-170 ◽  
Author(s):  
Jes Vollertsen ◽  
Asbjørn Haaning Nielsen ◽  
Henriette Stokbro Jensen ◽  
Tove Wium-Andersen ◽  
Thorkild Hvitved-Jacobsen

1969 ◽  
Vol 73 (4) ◽  
pp. 1158-1160 ◽  
Author(s):  
L. E. Compton ◽  
J. L. Gole ◽  
Richard McKelvy Martin

2008 ◽  
Vol 74 (21) ◽  
pp. 6746-6755 ◽  
Author(s):  
Zheming Wang ◽  
Chongxuan Liu ◽  
Xuelin Wang ◽  
Matthew J. Marshall ◽  
John M. Zachara ◽  
...  

ABSTRACT Because of their cell surface locations, the outer membrane c-type cytochromes MtrC and OmcA of Shewanella oneidensis MR-1 have been suggested to be the terminal reductases for a range of redox-reactive metals that form poorly soluble solids or that do not readily cross the outer membrane. In this work, we determined the kinetics of reduction of a series of Fe(III) complexes with citrate, nitrilotriacetic acid (NTA), and EDTA by MtrC and OmcA using a stopped-flow technique in combination with theoretical computation methods. Stopped-flow kinetic data showed that the reaction proceeded in two stages, a fast stage that was completed in less than 1 s, followed by a second, relatively slower stage. For a given complex, electron transfer by MtrC was faster than that by OmcA. For a given cytochrome, the reaction was completed in the order Fe-EDTA > Fe-NTA > Fe-citrate. The kinetic data could be modeled by two parallel second-order bimolecular redox reactions with second-order rate constants ranging from 0.872 μM−1 s−1 for the reaction between MtrC and the Fe-EDTA complex to 0.012 μM−1 s−1 for the reaction between OmcA and Fe-citrate. The biphasic reaction kinetics was attributed to redox potential differences among the heme groups or redox site heterogeneity within the cytochromes. The results of redox potential and reorganization energy calculations showed that the reaction rate was influenced mostly by the relatively large reorganization energy. The results demonstrate that ligand complexation plays an important role in microbial dissimilatory reduction and mineral transformation of iron, as well as other redox-sensitive metal species in nature.


2003 ◽  
Vol 58 (2) ◽  
pp. 417-427 ◽  
Author(s):  
S Ebrahimi ◽  
R Kleerebezem ◽  
M.C.M van Loosdrecht ◽  
J.J Heijnen

Sign in / Sign up

Export Citation Format

Share Document