TY - JOUR
T1 - Artificial methylotrophic cells via bottom-up integration of a methanol-utilizing pathway
AU - Wang, Ke
AU - Liu, Xueqing
AU - Hu, Kevin K.Y.
AU - Haritos, Victoria S.
N1 - Funding Information:
K.W. received MITS and MGS from Monash University. We thank the FlowCore Analysis Platform at Monash University for access to additional flow cytometry equipment. The authors acknowledge the Australian Research Council for financial support from Grant LE16100185. Schematic illustrations were created with BioRender.com .
Publisher Copyright:
© 2024 American Chemical Society
PY - 2024/3/15
Y1 - 2024/3/15
N2 - Methanol has gained substantial attention as a substrate for biomanufacturing due to plentiful stocks and nonreliance on agriculture, and it can be sourced renewably. However, due to inevitable complexities in cell metabolism, microbial methanol conversion requires further improvement before industrial applicability. Here, we present a novel, parallel strategy using artificial cells to provide a simplified and well-defined environment for methanol utilization as artificial methylotrophic cells. We compartmentalized a methanol-utilizing enzyme cascade, including NAD-dependent methanol dehydrogenase (Mdh) and pyruvate-dependent aldolase (KHB aldolase), in cell-sized lipid vesicles using the inverted emulsion method. The reduction of cofactor NAD+ to NADH was used to quantify the conversion of methanol within individual artificial methylotrophic cells via flow cytometry. Compartmentalization of the reaction cascade in liposomes led to a 4-fold higher NADH production compared with bulk enzyme experiments, and the incorporation of KHB aldolase facilitated another 2-fold increase above the Mdh-only reaction. This methanol-utilizing platform can serve as an alternative route to speed up methanol biological conversion, eventually shifting sugar-based bioproduction toward a sustainable methanol bioeconomy.
AB - Methanol has gained substantial attention as a substrate for biomanufacturing due to plentiful stocks and nonreliance on agriculture, and it can be sourced renewably. However, due to inevitable complexities in cell metabolism, microbial methanol conversion requires further improvement before industrial applicability. Here, we present a novel, parallel strategy using artificial cells to provide a simplified and well-defined environment for methanol utilization as artificial methylotrophic cells. We compartmentalized a methanol-utilizing enzyme cascade, including NAD-dependent methanol dehydrogenase (Mdh) and pyruvate-dependent aldolase (KHB aldolase), in cell-sized lipid vesicles using the inverted emulsion method. The reduction of cofactor NAD+ to NADH was used to quantify the conversion of methanol within individual artificial methylotrophic cells via flow cytometry. Compartmentalization of the reaction cascade in liposomes led to a 4-fold higher NADH production compared with bulk enzyme experiments, and the incorporation of KHB aldolase facilitated another 2-fold increase above the Mdh-only reaction. This methanol-utilizing platform can serve as an alternative route to speed up methanol biological conversion, eventually shifting sugar-based bioproduction toward a sustainable methanol bioeconomy.
KW - artificial cells
KW - bottom-up synthetic biology
KW - methanol utilization
KW - one-carbon metabolism
KW - synthetic cells
UR - https://www.scopus.com/pages/publications/85185604448
U2 - 10.1021/acssynbio.3c00683
DO - 10.1021/acssynbio.3c00683
M3 - Article
C2 - 38359048
AN - SCOPUS:85185604448
SN - 2161-5063
VL - 13
SP - 888
EP - 900
JO - ACS Synthetic Biology
JF - ACS Synthetic Biology
IS - 3
ER -