우한민 교수
Han Min Woo
성균관대학교 식품생명공학과 · 생화학·유전·분자생물학
연구실 소개
우한민 교수의 연구실은 광합성 세균인 시네코박터 엘롱가투스를 활용해 이산화탄소를 고부가가치 화학물질로 직접 전환하는 생태계 기반의 바이오공정 기술을 개발하고 있습니다. 주요 연구 방향은 CO₂를 원료로 사용하는 대사공학과 합성생물학 기반의 유전자 조절 시스템을 통해 효소 경로를 최적화하고, 테르펜류 및 사쿠레인 등 유망한 생체활성물질을 고수율로 생산하는 것입니다. 특히, CRISPRi 기반의 유전자 억제 기술과 SyneBrick 벡터 플랫폼을 활용해 다중 유전자 조절이 가능한 고도화된 세포공장 플랫폼을 구축하고 있습니다.
연구 현황
연구 성과 추이
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주요 논문
15This is the first demonstration of photosynthetic production of amorpha-4,11-diene from CO2 in cyanobacteria and production of squalene in S. elongatus PCC 7942. Our optimized modular OverMEP strain (SeHL33) with either co-expression of ADS or SQS demonstrated the highest production levels of amorpha-4,11-diene and squalene, which could expand the list of farnesyl diphosphate-derived isoprenoids from CO2 as bio-solar cell factories.
Myrcene, a monoterpene (C10), has gathered attention as a starting material for high-value compounds, such as geraniol/linalool and (-)-menthol. Metabolic engineering has been successfully applied to produce monoterpenes, such as pinene and limonene, at high levels in microbial hosts. However, microbial synthesis of myrcene has not yet been reported. Thus, we metabolically engineered Escherichia coli for production of myrcene by introducing a heterologous mevalonate pathway and overexpressing ta
In cyanobacteria, metabolic engineering using synthetic biology tools is limited to build a biosolar cell factory that converts CO<sub>2</sub> to value-added chemicals, as repression of essential genes has not been achieved. In this study, we developed a dCas12a-mediated CRISPR interference system (CRISPRi-dCas12a) in cyanobacteria that effectively blocked the transcriptional initiation by means of a CRISPR-RNA (crRNA) and 19-nt direct repeat, resulting in 53-94% gene repression. The repression
Cyanobacteria are oxygenic photosynthetic prokaryotes that are able to assimilate CO<sub>2</sub> using solar energy and water. Metabolic engineering of cyanobacteria has suggested the possibility of direct CO<sub>2</sub> conversion to value-added chemicals. However, engineering of cyanobacteria has been limited due to the lack of various genetic tools for expression and control of multiple genes to reconstruct metabolic pathways for biochemicals from CO<sub>2</sub>. Thus, we developed SyneBrick
Capture and conversion of CO2 to valuable chemicals is intended to answer global challenges on environmental issues, climate change and energy security. Engineered cyanobacteria have been enabled to produce industry-relevant chemicals from CO2 . However, the final products from cyanobacteria have often been mixed with fermented metabolites during dark fermentation. In this study, our engineering of Synechococcus elongatus PCC 7942 enabled continuous conversion of CO2 to volatile acetone as sole
High Resolution Image Download MS PowerPoint Slide Direct conversion of carbon dioxide (CO 2 ) to value-added chemicals by engineering of cyanobacteria has received attention as a sustainable strategy in food and chemical industries. Herein, Synechococcus elongatus PCC 7942, a model cyanobacterium, was engineered to produce α-farnesene from CO 2 . As a result of the lack of farnesene synthase (FS) activity in the wild-type cyanobacterium, we metabolically engineered S. elongatus PCC 7942 to expr
The push-and-pull strategy for metabolic engineering was successfully demonstrated in Synechococcus elongatus PCC 7942, a model photosynthetic bacterium, to produce squalene from CO 2 . Squalene synthase (SQS) was fused to either a key enzyme (farnesyl diphosphate synthase) of the methylerythritol phosphate pathway or the β-subunit of phycocyanin (CpcB1). Engineered cyanobacteria with expression of a fusion CpcB1-SQS protein showed a squalene production level (7.16 ± 0.05 mg/L/OD 730 ) that was
BACKGROUND: The construction of microbial cell factories requires cost-effective and rapid strain development through metabolic engineering. Recently, RNA-guided CRISPR technologies have been developed for metabolic engineering of industrially-relevant host. RESULTS: To demonstrate the application of the CRISPR interference (CRISPRi), we developed two-plasmid CRISPRi vectors and applied the CRISPRi in Corynebacterium glutamicum to repress single target genes and double target genes simultaneousl
High Resolution Image Download MS PowerPoint Slide Metabolic engineering of cyanobacteria has received attention as a sustainable strategy to convert carbon dioxide to fatty acid-derived chemicals that are widely used in the food and chemical industries. Herein, Synechococcus elongatus PCC 7942, a model cyanobacterium, was engineered for the first time to produce fatty acid ethyl esters (FAEEs) from CO 2 . Due to the lack of an endogenous ethanol production pathway and wax ester synthase (AftA)
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