De novo production of xanthohumol by a metabolically engineered Escherichia coli

Xanthohumol is a prenylflavonoid from hops with relevant bioactivities. Microbial production has emerged as a sustainable and potentially economic solution to produce it. Herein, we constructed a pathway for the de novo production of xanthohumol in Escherichia coli. Since the xanthohumol pathway depends on the availability of dimethylallyl pyrophosphate (DMAPP) and S-adenosylmethionine (SAM), SAM synthase (metK) was integrated into the genome of E. coli strains with previously engineered DMAPP pathways. Eleven prenyltransferases (PT) and the O-methyltransferase (OMT) from Humulus lupulus (HlOMT1) were tested. E. coli M-PAR-121:BlIDI:metK, constructed by integrating metK into the E. coli strain with integration of isopentenyl diphosphate isomerase (IDI) from Bacillus licheniformis (E. coli M-PAR-121:BlIDI) and expressing CdpC3PT from Neosartorya fischeri and HlOMT1 in combination with the naringenin chalcone pathway, was the best producer. This strain was able to produce 7.3 mg/L of desmethylxanthohumol and 5.3 mg/L of xanthohumol in the bioreactor, representing the first report of de novo production of xanthohumol in E. coli.

Publication Details

Journal
Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Published
2025-10-01
Primary Topic
Hops Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

De novo production of xanthohumol by a metabolically engineered Escherichia coli

Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Hops Chemistry and Applications
article

De novo production of xanthohumol by a metabolically engineered Escherichia coli

article en

Abstract

Xanthohumol is a prenylflavonoid from hops with relevant bioactivities. Microbial production has emerged as a sustainable and potentially economic solution to produce it. Herein, we constructed a pathway for the de novo production of xanthohumol in Escherichia coli. Since the xanthohumol pathway depends on the availability of dimethylallyl pyrophosphate (DMAPP) and S-adenosylmethionine (SAM), SAM synthase (metK) was integrated into the genome of E. coli strains with previously engineered DMAPP pathways. Eleven prenyltransferases (PT) and the O-methyltransferase (OMT) from Humulus lupulus (HlOMT1) were tested. E. coli M-PAR-121:BlIDI:metK, constructed by integrating metK into the E. coli strain with integration of isopentenyl diphosphate isomerase (IDI) from Bacillus licheniformis (E. coli M-PAR-121:BlIDI) and expressing CdpC3PT from Neosartorya fischeri and HlOMT1 in combination with the naringenin chalcone pathway, was the best producer. This strain was able to produce 7.3 mg/L of desmethylxanthohumol and 5.3 mg/L of xanthohumol in the bioreactor, representing the first report of de novo production of xanthohumol in E. coli.

Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Industry, innovation and infrastructure
Openalex Percentile: Top 33%
Hops Chemistry and Applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.