Skip to main content
. 2023 Dec 4;23:381. doi: 10.1186/s12866-023-03133-z

Table 1.

Transcription rates of metal transporters and metal-related genesa

Hfx. alexandrinus DSM 27206 ORFb Gene name Log2FC Annotation
0.1 mM 0.25 mM 0.5 mM
Hfx-2019-SC1-cds4 copA 3.25 4.48 5.64 Cu+-exporting ATPase
Hfx-2019-SC1-cds5 lrp - 2.2 3.73 Transcriptional regulator
Hfx-2019-SC1-cds6 copZ - - 3.1 Copper chaperone
Hfx-2019-SC1-cds149 petE 5.49 - - Plastocyanin/azurin family
Hfx-2019-SC1-cds430 3.14 - - HTH_ARSR domain containing protein
Hfx-2019-SC3-cds305 - - 2.09 HTH_ARSR domain containing protein
Hfx-2019-SC4-cds254 2.08 - 2.67 ABC.PE.A1 peptide/nickel transport system ATP-binding protein
Hfx-2019-SC4-cds255 - - 2.84 ABC.PE.A peptide/nickel transport system ATP-binding protein
Hfx-2019-SC4-cds257 - - 2.84 ABC.PE.P peptide/nickel transport system permease protein
Hfx-2019-SC4-cds258 ddpA - - 2.19 ABC.PE.S peptide/nickel transport system substrate-binding protein
Hfx-2019-SC4-cds326 petE - - 3.06 Plastocyanin/azurin family
Hfx-2019-SC5-cds117 mntH - - 2.43 Manganese transport protein
Hfx-2019-SC4-cds164 mobA - - -5.72 Molybdopterin-guanine dinucleotide biosynthesis protein A
Hfx-2019-SC4-cds165 wtpA - - -5.94 Molybdate/tungstate transport system substrate-binding protein
Hfx-2019-SC4-cds166 wtpB - - -5.15 Molybdate/tungstate transport system permease protein
Hfx-2019-SC4-cds220 - -2.68 - LucA/LucC family protein member
Hfx-2019-SC4-cds224 fepB -2.17 - - ABC.FEV.S iron complex transport system substrate-binding protein
Hfx-2019-SC4-cds239 cibT -2.16 - - Cobalt-precorrin-6B (C15)-methyltransferase
Hfx-2019-SC4-cds240 cbtB -2.9 - - Cobalt transporter subunit, putative
Hfx-2019-SC4-cds241 cbtA -2.83 - - Cobalt transporter subunit, putative
Hfx-2019-SC4-cds243 asnC -2.09 - - Lrp/AsnC family transcriptional regulator
Hfx-2019-SC4-cds337 -2 - - ABC.PE.P1 peptide/nickel transport system permease protein

aRNA-Seq was used to determine the expression levels of the genes in Hfx. alexandrinus DSM 27206, as detailed in the section on Materials and Methods. The data are the average of three replicates. The threshold of differential expression genes was: |log2(FoldChange)|> 1 and qvalue < 0.00. Dashes indicate that there were minimal changes to the transcription, not considered statistically significant. bThe gene name, number, and annotation were generated through the gDNA sequencing of the tested strain, as described in the Materials and Methods section