TY - JOUR
T1 - Amino Acid Self-Regenerating Cell-Free Protein Synthesis System that Feeds on PLA Plastics, CO2, Ammonium, and α-Ketoglutarate
AU - Nishikawa, Shota
AU - Yu, Wen Chi
AU - Jia, Tony Z.
AU - He, Ming Jing
AU - Khusnutdinova, Anna
AU - Yakunin, Alexander F.
AU - Chiang, Yin Ru
AU - Fujishima, Kosuke
AU - Wang, Po Hsiang
N1 - Publisher Copyright:
© 2024 The Authors. Published by American Chemical Society
PY - 2024/5/17
Y1 - 2024/5/17
N2 - Recent advances in synthetic biology have enabled the in vitro operation of the central dogma in the reconstituted cell-free protein synthesis system (i.e., the PURE system), which represents a convenient platform to address molecular-level biochemical questions and a robust workhorse for biomanufacturing of noncanonical peptides, polyketides, and enzymes that are difficult to express in vivo. However, unlike living cells regenerating their building blocks from substrates, PURE systems require an extra supply of 20 amino acids (AAs) for protein synthesis. Cell-free protein synthesis would be more cost-effective and environmentally friendly if the PURE systems could self-regenerate the protein building blocks (i.e., AAs) from a renewable feedstock, such as plastic waste. Here, we developed a renovated PURE system capable of self-regenerating aspartate, asparagine, glutamate, and glutamine using polylactate (PLA) plastics and α-ketoglutarate, CO2, and NH4+ as the AAs precursors. We first established a one-pot, cofactor self-sufficient multienzyme cascade to oxidize d l-PLA to (i) produce pyruvate as the precursor of aspartate and asparagine and (ii) regenerate NADH (reducing equivalents) for the reductive amination of α-ketoglutarate to yield glutamate and subsequent glutamine, the shared amine group donors for most AAs. Subsequently, the PLA-metabolic multienzyme cascade was introduced into the PURE system devoid of the four PLA-derived AAs. The PLA hydrolase-coding mRNA was translated in the modified PURE system, producing PLA hydrolase incorporating PLA-derived AAs. This enzyme further metabolizes PLA into more AAs for mRNA translation, forming a closed-loop circuit that seamlessly couples mRNA translation to AA metabolism. This process resembles a simplified heterotrophic life form, utilizing PLA both as building blocks and as reducing equivalents. Therefore, the “PLA-eating” PURE system established here offers a bioeconomy platform for valorizing PLA plastic for the future production of peptidyl biochemicals.
AB - Recent advances in synthetic biology have enabled the in vitro operation of the central dogma in the reconstituted cell-free protein synthesis system (i.e., the PURE system), which represents a convenient platform to address molecular-level biochemical questions and a robust workhorse for biomanufacturing of noncanonical peptides, polyketides, and enzymes that are difficult to express in vivo. However, unlike living cells regenerating their building blocks from substrates, PURE systems require an extra supply of 20 amino acids (AAs) for protein synthesis. Cell-free protein synthesis would be more cost-effective and environmentally friendly if the PURE systems could self-regenerate the protein building blocks (i.e., AAs) from a renewable feedstock, such as plastic waste. Here, we developed a renovated PURE system capable of self-regenerating aspartate, asparagine, glutamate, and glutamine using polylactate (PLA) plastics and α-ketoglutarate, CO2, and NH4+ as the AAs precursors. We first established a one-pot, cofactor self-sufficient multienzyme cascade to oxidize d l-PLA to (i) produce pyruvate as the precursor of aspartate and asparagine and (ii) regenerate NADH (reducing equivalents) for the reductive amination of α-ketoglutarate to yield glutamate and subsequent glutamine, the shared amine group donors for most AAs. Subsequently, the PLA-metabolic multienzyme cascade was introduced into the PURE system devoid of the four PLA-derived AAs. The PLA hydrolase-coding mRNA was translated in the modified PURE system, producing PLA hydrolase incorporating PLA-derived AAs. This enzyme further metabolizes PLA into more AAs for mRNA translation, forming a closed-loop circuit that seamlessly couples mRNA translation to AA metabolism. This process resembles a simplified heterotrophic life form, utilizing PLA both as building blocks and as reducing equivalents. Therefore, the “PLA-eating” PURE system established here offers a bioeconomy platform for valorizing PLA plastic for the future production of peptidyl biochemicals.
KW - bioplastic valorization
KW - cell-free biocatalysis
KW - cofactor self-sufficient
KW - green chemistry
KW - in vitro protein synthesis
KW - one-pot multienzyme cascade
KW - polylactic acid
KW - sustainable bioeconomy
UR - http://www.scopus.com/inward/record.url?scp=85192257875&partnerID=8YFLogxK
U2 - 10.1021/acscatal.4c00992
DO - 10.1021/acscatal.4c00992
M3 - 期刊論文
AN - SCOPUS:85192257875
SN - 2155-5435
VL - 14
SP - 7696
EP - 7706
JO - ACS Catalysis
JF - ACS Catalysis
IS - 10
ER -