TY - JOUR
T1 - Leveraging Engineered Pseudomonas putida Minicells for Bioconversion of Organic Acids into Short-Chain Methyl Ketones
AU - Kozaeva, Ekaterina
AU - Nieto-Domínguez, Manuel
AU - Tang, Kent Kang Yong
AU - Stammnitz, Maximilian
AU - Nikel, Pablo Iván
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society.
PY - 2025
Y1 - 2025
N2 - Methyl ketones, key building blocks widely used in diverse industrial applications, largely depend on oil-derived chemical methods for their production. Here, we investigated biobased production alternatives for short-chain ketones, adapting the solvent-tolerant soil bacterium Pseudomonas putida as a host for ketone biosynthesis either by whole-cell biocatalysis or using engineered minicells, chromosome-free bacterial vesicles. Organic acids (acetate, propanoate and butanoate) were selected as the main carbon substrate to drive the biosynthesis of acetone, butanone and 2-pentanone. Pathway optimization identified efficient enzyme variants from Clostridium acetobutylicum and Escherichia coli, tested with both constitutive and inducible expression of the cognate genes. By implementing these optimized pathways in P. putida minicells, which can be prepared through a simple three-step purification protocol, the feedstock was converted into the target short-chain methyl ketones. These results highlight the value of combining morphology and pathway engineering of noncanonical bacterial hosts to establish alternative bioprocesses for toxic chemicals that are difficult to produce by conventional approaches.
AB - Methyl ketones, key building blocks widely used in diverse industrial applications, largely depend on oil-derived chemical methods for their production. Here, we investigated biobased production alternatives for short-chain ketones, adapting the solvent-tolerant soil bacterium Pseudomonas putida as a host for ketone biosynthesis either by whole-cell biocatalysis or using engineered minicells, chromosome-free bacterial vesicles. Organic acids (acetate, propanoate and butanoate) were selected as the main carbon substrate to drive the biosynthesis of acetone, butanone and 2-pentanone. Pathway optimization identified efficient enzyme variants from Clostridium acetobutylicum and Escherichia coli, tested with both constitutive and inducible expression of the cognate genes. By implementing these optimized pathways in P. putida minicells, which can be prepared through a simple three-step purification protocol, the feedstock was converted into the target short-chain methyl ketones. These results highlight the value of combining morphology and pathway engineering of noncanonical bacterial hosts to establish alternative bioprocesses for toxic chemicals that are difficult to produce by conventional approaches.
KW - 2-pentanone
KW - Acetone
KW - Butanone
KW - Ketones
KW - Metabolic engineering
KW - Minicells
KW - Pseudomonas putida
KW - Synthetic biology
U2 - 10.1021/acssynbio.4c00700
DO - 10.1021/acssynbio.4c00700
M3 - Journal article
C2 - 39748701
AN - SCOPUS:85215085225
SN - 2161-5063
VL - 14
SP - 257
EP - 272
JO - ACS Synthetic Biology
JF - ACS Synthetic Biology
IS - 1
ER -