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The transcript level of desB in wild-type strain EC1, dzrR mutant, and complementation strain dzrR (pBB- dzrR ) monitored by RT-qPCR assay. Fold change of desB expression was analyzed using 2 -∆∆C T method, with 16S rRNA gene serving as the endogenous control and the wild-type strain EC1 as the reference sample. Data are presented as mean SE, n = 4. Statistical analysis was performed using permutation test versus the wild-type strain EC1. * P < 0.05

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