Table 1.
Selection of sgRNA clones enriched by droplet sorting.
sgRNA | Appearances | Effect on growth | Gene function |
---|---|---|---|
gdhA_25* | 4 | None | Glutamate dehydrogenase |
ssr2016_62* | 3 | Impaired | Ferredoxin:plastoquinone reductase, cyclic electron flow |
gltA_41* | 3 | Impaired | Citrate synthase |
pntB_19 | 3 | None | Transhydrogenase subunit |
pcnB_64* | 3 | Impaired | Nucleotidyltransferase |
serA_10* | 2 | Impaired | Phosphoglycerate dehydrogenase |
gltB_3* | 2 | Impaired | Glutamate synthase |
ndhD2_15 | 2 | None | NDH-1 complex subunit, cyclic electron flow |
sdhB_26* | 2 | None | Succinate dehydrogenase |
Entry85_13 | 2 | None | atpA (ATP synthase) asRNA |
pstC_41 | 2 | None | Phosphate transporter |
slr0453_10 | 2 | None | Phosphoketolase |
Note: Mutants were identified from a CRISPRi library based on L-lactate productivity. Appearance is the number of sorting runs (out of four) where that clone had an enrichment factor of at least 2 (normalized abundance in sorted population/normalized abundance in unsorted population). Clones where growth was impaired are denoted. These clones were significantly depleted in the L300 dataset after four generations (ssr2016_62, padj = 1.6e−94; gltA_41, padj = 3.1e−53; pcnB_64, padj = 1.5e−58; serA_10, padj = 3.6e−21; gltB_3, padj = 0.015; multiple-hypothesis adjusted p-values calculated by DESeq2). An asterisk denotes sgRNA mutants selected for reconstruction and validation. Source data are provided as a Source Data file.