TY - JOUR
T1 - Changes in metabolic pathways of Desulfovibrio alaskensis G20 cells induced by molybdate excess
AU - Nair, Rashmi R.
AU - Silveira, Célia Marisa Costa Figueiredo
AU - Diniz, Mário S.
AU - Almeida, Maria Gabriela Machado de
AU - Moura, Jose J G
AU - Rivas, Maria G.
N1 - Sem PDF.
Fundacao para a Ciencia e Tecnologia (EXPL/BBB-BEP/0274/2012; SRFH/BPD/63061/2009; SRFH/BPD/79566/2011)
PY - 2015
Y1 - 2015
N2 - The activity of sulfate-reducing bacteria (SRB) intensifies the problems associated to corrosion of metals and the solution entails significant economic costs. Although molybdate can be used to control the negative effects of these organisms, the mechanisms triggered in the cells exposed to Mo-excess are poorly understood. In this work, the effects of molybdate ions on the growth and morphology of the SRB Desulfovibrio alaskensis G20 (DaG20) were investigated. In addition, the cellular localization, ion uptake and regulation of protein expression were studied. We found that molybdate concentrations ranging between 50 and 150 μM produce a twofold increase in the doubling time with this effect being more significant at 200 μM molybdate (five times increase in the doubling time). It was also observed that 500 μM molybdate completely inhibits the cellular growth. On the context of protein regulation, we found that several enzymes involved in energy metabolism, cellular division and metal uptake processes were particularly influenced under the conditions tested. An overall description of some of the mechanisms involved in the DaG20 adaptation to molybdate-stress conditions is discussed.
AB - The activity of sulfate-reducing bacteria (SRB) intensifies the problems associated to corrosion of metals and the solution entails significant economic costs. Although molybdate can be used to control the negative effects of these organisms, the mechanisms triggered in the cells exposed to Mo-excess are poorly understood. In this work, the effects of molybdate ions on the growth and morphology of the SRB Desulfovibrio alaskensis G20 (DaG20) were investigated. In addition, the cellular localization, ion uptake and regulation of protein expression were studied. We found that molybdate concentrations ranging between 50 and 150 μM produce a twofold increase in the doubling time with this effect being more significant at 200 μM molybdate (five times increase in the doubling time). It was also observed that 500 μM molybdate completely inhibits the cellular growth. On the context of protein regulation, we found that several enzymes involved in energy metabolism, cellular division and metal uptake processes were particularly influenced under the conditions tested. An overall description of some of the mechanisms involved in the DaG20 adaptation to molybdate-stress conditions is discussed.
KW - Hydrogen cycling
KW - Microbiologically influenced corrosion
KW - Molybdenum
KW - Sulfate-reducing bacteria
KW - Tungsten
UR - http://www.scopus.com/inward/record.url?scp=84925520023&partnerID=8YFLogxK
U2 - 10.1007/s00775-014-1224-4
DO - 10.1007/s00775-014-1224-4
M3 - Article
C2 - 25488518
AN - SCOPUS:84925520023
SN - 0949-8257
VL - 20
SP - 311
EP - 322
JO - JBIC Journal of Biological Inorganic Chemistry
JF - JBIC Journal of Biological Inorganic Chemistry
IS - 2
T2 - 2013 Molybdenum and Tungsten Enzymes Conference
Y2 - 16 July 2013 through 19 July 2013
ER -