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. 2020 Apr 3;11:1666. doi: 10.1038/s41467-020-15491-7

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.