Metabolic engineering of Corynebacterium glutamicum for L-cysteine production.
C. glutamicum
Feedback-insensitive CysEs
L-Cysteine production
L-Cysteine transporters
L-Serine biosynthesis
Thiosulfate
Journal
Applied microbiology and biotechnology
ISSN: 1432-0614
Titre abrégé: Appl Microbiol Biotechnol
Pays: Germany
ID NLM: 8406612
Informations de publication
Date de publication:
Feb 2019
Feb 2019
Historique:
received:
27
07
2018
accepted:
28
11
2018
revised:
26
11
2018
pubmed:
20
12
2018
medline:
31
5
2019
entrez:
20
12
2018
Statut:
ppublish
Résumé
L-cysteine, a valuable sulfur-containing amino acid, has been widely used in food, agriculture, and pharmaceutical industries. Due to the toxicity and complex regulation of L-cysteine, no efficient cell factory has yet been achieved for L-cysteine industrial production. In this study, the food-grade microorganism Corynebacterium glutamicum was engineered for L-cysteine production. Through deletion of the L-cysteine desulfhydrases (CD) and overexpression of the native serine acetyltransferase (CysE), the initial L-cysteine-producing strain CYS-2 was constructed to produce 58.2 ± 5.1 mg/L of L-cysteine. Subsequently, several metabolic engineering strategies were performed to further promote L-cysteine biosynthesis, including using strong promoter tac-M to enhance expression intensity of CysE, investigating the best candidate among several heterogeneous feedback-insensitive CysEs for L-cysteine biosynthesis, overexpressing L-cysteine synthase (CysK) to drive more metabolic flux, evaluating the efflux capacity of several heterogeneous L-cysteine transporters, engineering L-serine biosynthesis module to increase the precursor L-serine level and using thiosulfate as the sulfur source. Finally, the L-cysteine concentration of the engineered strain CYS-19 could produce 947.9 ± 46.5 mg/L with addition of 6 g/L Na
Identifiants
pubmed: 30564850
doi: 10.1007/s00253-018-9547-7
pii: 10.1007/s00253-018-9547-7
doi:
Substances chimiques
Serine O-Acetyltransferase
EC 2.3.1.30
Cysteine Synthase
EC 2.5.1.47
Cystathionine gamma-Lyase
EC 4.4.1.1
Cysteine
K848JZ4886
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1325-1338Subventions
Organisme : National Natural Science Foundation of China
ID : No. 31500044
Organisme : Natural Science Foundation of Tianjin City
ID : 17JCQNJC09600
Organisme : Natural Science Foundation of Tianjin City
ID : No. 17JCYBJC24000
Organisme : Hebei Normal University of Science and Technology
ID : ZD2017047
Organisme : Tianjin Science and Technology Committee
ID : 15PTCYSY00020