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. 2019 Oct 30;85(22):e01443-19. doi: 10.1128/AEM.01443-19

TABLE 1.

Genes and primers used in the qRT-PCR assay

Gene Annotation Primer sequence (5′–3′)
Forward Reverse
Primer for the oxidoreductase gene
    ZMO1116 Oxidoreductase TGTGGTTTGGGCCATCCG TGTCGGTGCGTCCTGTTTGT
    ZMO1772 NAD(P)H quinone oxidoreductase GGTCGCCTTGTCATTGTCG GGCTGTTCTGGCACGCAT
    ZMO1885 NADH flavin oxidoreductase TGGAGTGATGCCCAAGTAGAAG CACTGACATTAGACGGCACCATA
Primer for the reductase gene
    ZMO1993 NADPH quinone reductase GCGGTGTCGGTAGCTTGTT GCCTTCGCCGTGATTCTG
    ZMO0833 UDP-N-acetylenolpyruvoylglucosamine reductase ATCGCCTGCGTTGTGGTG GCATTCATGCGGATCATACCA
    ZMO1222 3-Oxoacyl-(acyl-carrier-protein) reductase TTAGCCGTGCCGTCATCAGA CGATCATGCCTGCCTTTGC
    ZMO1303 Pyrroline-5-carboxylate reductase ACAACCCTGATTTCTATTCTTGCC AACAACGCCCTTCCCTAACG
    ZMO1984 Aldo-keto reductase TCGCCATTTGTCAGCCTATC CAGCAAAGTTACTGCTACCCAC
    ZMO1254 Redoxin domain-containing protein CGCTATGGTAATCCCTATCAGGC GCTCATAAGCTGTGGCAAATCC
Primer for the dehydrogenase gene
    ZMO1335 NAD(P)H dehydrogenase (quinone) CCCGATTTGGGCGTTTG AGACCGCTCCGACCTTTCC
    ZMO1949 NAD(P)H dehydrogenase (quinone) TGGAGGCAAGCGGTTCTAC GCAACAGCGGTTTGAGCAT
    ZMO0157 d-Isomer-specific 2-hydroxyacid dehydrogenase TATGGCTGTCGGGTTATTCC TTCGGCGATGGCTTGG
    ZMO0788 d-Sorbitol dehydrogenase CAGTTGTCACGGTCGCAATG GCCGCAATCTGACTATCGTTTA
    ZMO1576 Short-chain dehydrogenase/reductase TCTATCGTCGCTAAGGGTGGTC GCTGCAATCCCATAAAGAACG
    ZMO1696 Zinc-binding alcohol dehydrogenase TCCGAAGACAGGCGAAGAATG CCTCGTCACCGACCTTAAATAGC
Primer for other genes
    ZMO1399 Fatty acid hydroxylase GAAACGGATTCACTATGACCAC CCGACAGCATAACCGATACA
    ZMO0020 Hypothetical protein CCGATCTAGTAAGCCAATTCACC TTTCAAATCTGTTGGTTGGGTGT
    ZMO0021 Hypothetical protein CCACTTCATATCGCTTCTGTCG GCGTAATCGGTGATCCCAAA
    ZMO0074 Hypothetical protein CGATAAAGACCGCCCGACC TCGCCAAGCAGGCATTCG
    ZMO1821 Hypothetical protein AGAAAGCCGCCGCCATC CACCATCATACCAACTGTCAACG
    ZMOr003a 16S rRNA gene TTAAGTTGGGCACTTTAGAGGAAC TGTCACCGCCATTGTAGCAC
a

The 16S rRNA gene ZMOr003 was used as the internal control to normalize the difference of the data.