Abstract

BackgroundKlebsiella pneumoniae is a promising industrial species for bioproduction of bulk chemicals such as 1,3-propanediol, 2,3-butanediol and 3-hydroxypropionic acid (3-HP). However, lactic acid is a troublesome by-product when optimizing for 3-HP production. Therefore, it is highly desirable to minimize lactic acid.ResultsHere, we show that lactic acid synthesis can be largely blocked by an engineered CRISPR interference (CRISPRi) system in K. pneumoniae. EGFP was recruited as a reporter of this CRISPRi system. Fluorescence assay of this CRISPRi system showed that enhanced green fluorescent protein (EGFP) expression level was repressed by 85–90%. To further test this CRISPRi system, guide RNAs were designed to individually or simultaneously target four lactate-producing enzyme genes. Results showed that all lactate-producing enzyme genes were significantly repressed. Notably, d-lactate dehydrogenase (ldhA) was shown to be the most influential enzyme for lactic acid formation in micro-aerobic conditions, as inhibiting ldhA alone led to lactic acid level similar to simultaneously repressing four genes. In shake flask cultivation, the strain coexpressing puuC (an aldehyde dehydrogenase catalyzing 3-hydroxypropionaldehyde to 3-HP) and dCas9-sgRNA inhibiting ldhA produced 1.37-fold 3-HP relative to the reference strain. Furthermore, in bioreactor cultivation, this CRISPRi strain inhibiting ldhA produced 36.7 g/L 3-HP, but only generated 1 g/L lactic acid. Clearly, this engineered CRISPRi system largely simplified downstream separation of 3-HP from its isomer lactic acid, an extreme challenge for 3-HP bioprocess.ConclusionsThis study offers a deep understanding of lactic acid metabolism in diverse species, and we believe that this CRISPRi system will facilitate biomanufacturing and functional genome studies of K. pneumoniae or beyond.

Highlights

  • Klebsiella pneumoniae is a promising industrial species for bioproduction of bulk chemicals such as 1,3-propanediol, 2,3-butanediol and 3-hydroxypropionic acid (3-HP)

  • ­T1 and ­T2 respectively displayed 85 and 90% inhibition on enhanced green fluorescent protein (EGFP) level when aTc was added into medium. Overall these results indicated that CRISPR interference (CRISPRi) system significantly repressed EGFP expression, tet promoter failed to tightly control dCas9 expression in K. pneumoniae

  • Fluorescence assay of dCas9‐gRNA‐mediated transcription repression in K. pneumoniae The dCas9 was derived from Streptococcus pyogenes, and CRISPRi system was developed to dissect lactic acid metabolism

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Summary

Introduction

Klebsiella pneumoniae is a promising industrial species for bioproduction of bulk chemicals such as 1,3-propanediol, 2,3-butanediol and 3-hydroxypropionic acid (3-HP). It is highly desirable to minimize lactic acid. Byproducts are problematic because they consume cellular resources and entangle downstream separation. Conventional genetic engineering strategies to attenuate byproducts formation mainly rely on deletion or repression of their biosynthesis genes [1,2,3,4]. These approaches in most cases compromise cell growth which in turn hampers the production of desired metabolites [5].

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