Metabolic engineering of beta-oxidation in Penicillium chrysogenum for improved semi-synthetic cephalosporin biosynthesis


Autoria(s): Veiga, Tania; Gombert, Andreas Karoly; Landes, Nils; Verhoeven, Maarten D.; Kiel, Jan A. K. W.; Krikken, Arjen M.; Nijland, Jeroen G.; Touw, Hesselien; Luttik, Marijke A. H.; Van der Toorn, John C.; Driessen, Arnold J. M.; Bovenberg, Roel A. L.; Van den Berg, Marco A.; Van der Klei, Ida J.; Pronk, Jack T.; Daran, Jean-Marc
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

Industrial production of semi-synthetic cephalosporins by Penicillium chrysogenum requires supplementation of the growth media with the side-chain precursor adipic acid. In glucose-limited chemostat cultures of P. chrysogenum, up to 88% of the consumed adipic acid was not recovered in cephalosporinrelated products, but used as an additional carbon and energy source for growth. This low efficiency of side-chain precursor incorporation provides an economic incentive for studying and engineering the metabolism of adipic acid in P. cluysogenum. Chemostat-based transcriptome analysis in the presence and absence of adipic acid confirmed that adipic acid metabolism in this fungus occurs via beta-oxidation. A set of 52 adipate-responsive genes included six putative genes for acyl-CoA oxidases and dehydrogenases, enzymes responsible for the first step of beta-oxidation. Subcellular localization of the differentially expressed acyl-CoA oxidases and dehydrogenases revealed that the oxidases were exclusively targeted to peroxisomes, while the dehydrogenases were found either in peroxisomes or in mitochondria. Deletion of the genes encoding the peroxisomal acyl-CoA oxidase Pc20g01800 and the mitochondrial acyl-CoA dehydrogenase Pc20g07920 resulted in a 1.6- and 3.7-fold increase in the production of the semi-synthetic cephalosporin intermediate adipoyl-6-APA, respectively. The deletion strains also showed reduced adipate consumption compared to the reference strain, indicating that engineering of the first step of beta-oxidation successfully redirected a larger fraction of adipic acid towards cephalosporin biosynthesis. (C) 2012 Elsevier Inc. All rights reserved.

Netherlands Organization for Scientific Research (NWO) via IBOS (Integration of Biosynthesis and Organic Synthesis) Program of Advanced Chemical Technologies for Sustainability (ACTS) [IBOS 053.63.011]

Netherlands Organization for Scientific Research (NWO) via IBOS (Integration of Biosynthesis and Organic Synthesis) Program of Advanced Chemical Technologies for Sustainability (ACTS)

Netherlands Ministry of Economic Affairs

Netherlands Ministry of Economic Affairs

B-Basic partner organizations through B-Basic

BBasic partner organizations through BBasic

publicprivate NWOACTS program (ACTS: Advanced Chemical Technologies for Sustainability)

public-private NWO-ACTS program (ACTS: Advanced Chemical Technologies for Sustainability)

Identificador

Metabolic Engineerng, San Diego, v. 14, n. 4, supl. 1, Part 4, p. 437-448, July, 2012

1096-7176

http://www.producao.usp.br/handle/BDPI/41775

10.1016/j.ymben.2012.02.004

http://dx.doi.org/10.1016/j.ymben.2012.02.004

Idioma(s)

eng

Publicador

ACADEMIC PRESS INC ELSEVIER SCIENCE

San Diego

Relação

Metabolic Engineering

Direitos

closedAccess

Copyright ACADEMIC PRESS INC ELSEVIER SCIENCE

Palavras-Chave #PENICILLIUM CHRYSOGENUM #BETA-LACTAMS #CEPHALOSPORINS #BETA-OXIDATION #ADIPIC ACID #METABOLIC ENGINEERING #CHAIN DICARBOXYLIC-ACIDS #CLAVULIGERUS CEFE GENE #ACYL-COA OXIDASE #C-14 ADIPIC ACID #SACCHAROMYCES-CEREVISIAE #ASPERGILLUS-NIDULANS #STREPTOMYCES-CLAVULIGERUS #FATTY-ACIDS #HUMAN-URINE #PEROXISOME PROLIFERATION #BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Tipo

article

original article

publishedVersion