Fig. 2

Xoo sRNAs differentially expressed under two culture conditions. Presented sRNAs were identified by high-throughput sRNA sequencing of RNA samples from Xoo cultures on PSA and XOM2 media, respectively. Fold change was calculated as Log2 ratio of sRNA transcript quantity between XOM2 and PSA cultures. The expression level of every sRNA was normalized to be the transcript per million (TPM)