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. 2019 Jul 19;10:1642. doi: 10.3389/fmicb.2019.01642

TABLE 1.

Bacterial strains and plasmids used in this study.

Strain or plasmid Genotype References or sources
At. ferrooxidans
ATCC 23270 Wild type
Escherichia coli
JM109 endA1, recA1, gyrA96, thi, hsdR17 (rk–, mk+), relA1, supE44, Δ(lac-proAB), [F′ traD36, proAB, laqIqZΔM15] Promega
BL21 F-, ompT, hsdSB (rB-mB-), gal, dcm, rne131, (DE3) Invitrogen
PK22 hsdS, gaL λDE53, Δcrp-bs990, rpsL, Δfnr, zcj-3061::Tn10 Lazazzera et al., 1993
RZ7350 lacZ Δ145, narG234::MudI1734 Kiley and Reznikoff, 1991
RZ8480 Δfnr, lacZ Δ145, narG234::MudI1734 Lazazzera et al., 1993
Plasmids
pET100/D-TOPO Expression vector Invitrogen
pET100/D-TOPO FNRAF Expression vector, FNRAF protein This study
pKK223-3 Plasmid vector, Ampr PL-Pharmacia
pKK223-3 fnrAF fnrAF coding region cloned into pKK223-3 vector with a tac promoter This study
pET11A Expresion vector, Ampr with a T7 promoter Novagen
pET11A fnrAF fnrAF coding region cloned into pET11A vector with a T7 promoter This study