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Metabolic engineering of "last-line antibiotic" colistin in Paenibacillus polymyxa.
Chen, Nanzhu; Cai, Peiyan; Zhang, Dengwei; Zhang, Junliang; Zhong, Zheng; Li, Yong-Xin.
Afiliación
  • Chen N; Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
  • Cai P; Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
  • Zhang D; Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
  • Zhang J; Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
  • Zhong Z; Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
  • Li YX; Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China. Electronic address: yxpli@hku.hk.
Metab Eng ; 85: 35-45, 2024 Sep.
Article en En | MEDLINE | ID: mdl-39019251
ABSTRACT
Colistin, also known as polymyxin E, is a lipopeptide antibiotic used to treat infections caused by multidrug-resistant gram-negative bacteria. It is considered a "last-line antibiotic", but its clinical development is hindered by low titer and impurities resulting from the presence of diverse homologs in microbial fermentation. To ensure consistent pharmaceutical activity and kinetics, it is crucial to have high-purity colistin active pharmaceutical ingredient (API) in the pharmaceutical industry. This study focused on the metabolic engineering of a natural colistin producer strain to produce colistin with a high titer and purity. Guided by genome mining, we identified Paenibacillus polymyxa ATCC 842 as a natural colistin producer capable of generating a high proportion of colistin A. By systematically inactivating seven non-essential biosynthetic gene clusters (BGCs) of peptide metabolites that might compete precursors with colistin or inhibit colistin production, we created an engineered strain, P14, which exhibited an 82% increase in colistin titer and effectively eliminated metabolite impurities such as tridecaptin, paenibacillin, and paenilan. Additionally, we engineered the L-2,4-diaminobutyric acid (L-2,4-DABA) pathway to further enhance colistin production, resulting in the engineered strain P19, which boosted a remarkable colistin titer of 649.3 mg/L - a 269% improvement compared to the original strain. By concurrently feeding L-isoleucine and L-leucine, we successfully produced high-purity colistin A, constituting 88% of the total colistin products. This study highlights the potential of metabolic engineering in improving the titer and purity of lipopeptide antibiotics in the non-model strain, making them more suitable for clinical use. These findings indicate that efficiently producing colistin API in high purity directly from fermentation can now be achieved in a straightforward manner.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Colistina / Ingeniería Metabólica / Paenibacillus polymyxa / Antibacterianos Idioma: En Revista: Metab Eng Asunto de la revista: ENGENHARIA BIOMEDICA / METABOLISMO Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Bélgica

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Colistina / Ingeniería Metabólica / Paenibacillus polymyxa / Antibacterianos Idioma: En Revista: Metab Eng Asunto de la revista: ENGENHARIA BIOMEDICA / METABOLISMO Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Bélgica