Enhancement of Lycopene Biosynthesis Using Self-Assembled Multi-Enzymic Protein Cages

Constructions of self-assembled protein nanocages for enzyme immobilization and cargo transport are very promising in biotechnology fields such as natural product biosynthesis. Here, we present an engineered isopentenyl pyrophosphate (IPP) synthetic nanocage with multiple enzymes for lycopene production in bacteria. The enzymes involved in IPP biosynthesis (ScCK, AtIPK, and MxanIDI) were assembled onto the exterior of an engineered protein cage based on α-carboxysome. The IPP synthetic nanocage was co-expressed with CrtE/CrtB/CrtI in <i>Escherichia coli</i>. This approach increased the metabolic flux and resulted in a 1.7-fold increase in lycopene production in the engineered <i>E</i>. <i>coli</i> compared with the control strain. The results provide insights into the immobilization and assembling of IPP biosynthetic enzymes in protein nanocages, which serve as a powerful tool for achieving efficient synthesis of lycopene.

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Publication Details

Journal
Microorganisms
Published
2025-03-26
DOI
https://doi.org/10.3390/microorganisms13040747
Citations
3
Primary Topic
Plant biochemistry and biosynthesis
Type
article
Field-Weighted Citation Impact
2.42
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article

Enhancement of Lycopene Biosynthesis Using Self-Assembled Multi-Enzymic Protein Cages

Ning Yu, Binqiang Wang, Bing Tian, F. Zhang et al.
3 citations
Microorganisms
Plant biochemistry and biosynthesis
2.42
article

Enhancement of Lycopene Biosynthesis Using Self-Assembled Multi-Enzymic Protein Cages

Ning Yu, Binqiang Wang, Bing Tian, F. Zhang, Yonghua Yao, Yulong Zhou
article en
3 citations

Abstract

Constructions of self-assembled protein nanocages for enzyme immobilization and cargo transport are very promising in biotechnology fields such as natural product biosynthesis. Here, we present an engineered isopentenyl pyrophosphate (IPP) synthetic nanocage with multiple enzymes for lycopene production in bacteria. The enzymes involved in IPP biosynthesis (ScCK, AtIPK, and MxanIDI) were assembled onto the exterior of an engineered protein cage based on α-carboxysome. The IPP synthetic nanocage was co-expressed with CrtE/CrtB/CrtI in <i>Escherichia coli</i>. This approach increased the metabolic flux and resulted in a 1.7-fold increase in lycopene production in the engineered <i>E</i>. <i>coli</i> compared with the control strain. The results provide insights into the immobilization and assembling of IPP biosynthetic enzymes in protein nanocages, which serve as a powerful tool for achieving efficient synthesis of lycopene.

MicroorganismsVol. 13(4)
Shihezi University (CN), Xinjiang Production and Construction Corps (CN), Institute of Biophysics (CN), Zhejiang University (CN)
Responsible consumption and production
Openalex Percentile: Top 12%
Plant biochemistry and biosynthesis
2.42
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