Steps towards the synthetic biology of polyketide biosynthesis. - Wikidata - awgldk - TriplyDB

Steps towards the synthetic biology of polyketide biosynthesis.

Steps towards the synthetic biology of polyketide biosynthesis.

http://www.wikidata.org/entity/Q38174180

about

Synthetic biology for pharmaceutical drug discovery Second-generation probes for biosynthetic intermediate capture: towards a comprehensive profiling of polyketide assembly Insights into 6-Methylsalicylic Acid Bio-assembly by Using Chemical Probes Roles of type II thioesterases and their application for secondary metabolite yield improvement.Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases.Chemical probes for the functionalization of polyketide intermediates.Breaking a pathogen's iron will: Inhibiting siderophore production as an antimicrobial strategy Insights into 6-Methylsalicylic Acid Bio-assembly by Using Chemical Probes.Precision multidimensional assay for high-throughput microRNA drug discovery Synthetic Biology of Natural Products.Complete genome sequencing and antibiotics biosynthesis pathways analysis of Streptomyces lydicus 103.Recent advances in combinatorial biosynthesis for drug discovery Synthetic biology advances for pharmaceutical production.Pseudomonas putida-a versatile host for the production of natural products.The biosynthetic pathway of FK506 and its engineering: from past achievements to future prospects.Genetic engineering of modular PKSs: from combinatorial biosynthesis to synthetic biology.Strategies for the Discovery and Development of New Antibiotics from Natural Products: Three Case Studies.The Conformational Flexibility of the Acyltransferase from the Disorazole Polyketide Synthase Is Revealed by an X-ray Free-Electron Laser Using a Room-Temperature Sample Delivery Method for Serial Crystallography.Engineered polyketides: Synergy between protein and host level engineering.Output ordering and prioritisation system (OOPS): ranking biosynthetic gene clusters to enhance bioactive metabolite discovery.

P2860

Q26775582-CB49B5D3-710A-49C6-B71E-8F4B49D6208C Q28822516-B4B76ADE-7875-4D18-A957-3A3C9AF67E5C Q28829669-E412B671-D3C2-4FB7-8414-65FD6E8269DD Q34100622-76EF5725-50D2-4733-8590-2CD344F53434 Q34120045-EE02C2E0-F784-46DA-AC47-03D892F2A789 Q35248736-68F2E7F8-5E1A-4889-BDAB-7DDFB28322D5 Q35688927-95CABA8D-B938-4AD1-8397-62EEB9760197 Q35911523-742A4677-97F2-492E-84B5-4BB7B128B711 Q35924586-3464F25E-E040-4791-8A55-403B0D0B64DF Q36098396-15A5FC15-1C2E-4DA7-84E7-8B33F69EADAA Q37710901-F81EED78-56F5-4FB1-B5AB-A214B50928A8 Q38364681-052731A4-7FBD-48F4-86FC-71822E229644 Q38368454-429F2B5C-5CB6-48E0-9DBA-281B871CE93D Q38534411-E2024E73-E108-4E13-A36D-EE4EC7A8CE74 Q38581311-EE5771B6-03A0-4A78-B959-B7E967B3B051 Q38629855-C4CA25E1-7DF4-45A9-8BF6-E0EAF0B8DB51 Q38980013-C46A97F3-02E1-495B-BA56-65D6C13DE708 Q46361736-1BE8A77D-5618-45EF-8858-1E525BD761EC Q47215208-DEC7A5AC-45B7-4B87-A81F-B6E1E7F4B534 Q47236080-582E37E7-6A48-4232-85CB-A04FB1EC705B

P2860

Steps towards the synthetic biology of polyketide biosynthesis.

http://www.wikidata.org/entity/Q38174180

description

article científic

@ca

article scientifique

@fr

articol științific

@ro

articolo scientifico

@it

artigo científico

@gl

artigo científico

@pt

artigo científico

@pt-br

artikel ilmiah

@id

artikull shkencor

@sq

artículo científico

@es

name

Steps towards the synthetic biology of polyketide biosynthesis.

@en

type

label

Steps towards the synthetic biology of polyketide biosynthesis.

@en

prefLabel

Steps towards the synthetic biology of polyketide biosynthesis.

@en

P1433

Q38174180-4B1E337E-D1E6-4867-92E7-262E1989CB66

P1476

Q38174180-29548A2F-774C-48AB-81D4-DD619E08B822

P2093

Q38174180-7A331D85-8C72-4507-A730-A844C7E76D1F

P275

Q38174180-490207D2-2EB4-4142-8976-38AB9A919CED

P2860

Q38174180-02E58A0A-B999-4E1C-A421-F685DCA75B0F

Q38174180-0655CF7E-68E9-44AE-A8E7-BA1060DF4F41

Q38174180-0BE1E1B8-0543-4B36-8500-524D7229D9EA

Q38174180-12DBA539-2C32-44EB-B2C3-964B322474A0

Q38174180-13EEAE04-1650-4A0B-BD6F-4E989391EFB8

Q38174180-14A022C9-ECAC-423E-A0D9-FD289D02F031

Q38174180-19620ABF-4363-46E4-B426-366AD0B9E380

Q38174180-1B0E72AA-D605-48FB-A0E1-EDD7F7E83AFC

Q38174180-1CEE0039-82F5-4C12-B259-F83144D9D510

Q38174180-1E767689-975B-43B9-A1BB-0ED190230309

P304

Q38174180-460307B5-C3BB-4F70-86B9-CB99A6948BCE

P31

Q38174180-4D9B093D-406B-4EFF-A787-8369F4DB3853

Q38174180-72D7043F-A7E9-43F3-B2C2-8AA41A5818EB

P356

Q38174180-C06F3FBC-ED74-416D-BB05-87BE0CEEB055

P433

Q38174180-DD5F2AC8-D793-431F-A7D9-0B3A368E9A51

P478

Q38174180-C7BC6A18-4EFB-4496-8271-8987CF9EA334

P50

Q38174180-2539793A-BF5E-41F3-A351-DFF964DBA2F7

Q38174180-5468992B-D892-4C69-BA80-250578B678AC

P577

Q38174180-30A78CF9-2214-4B39-8571-DD8C6A86B21B

Q38174180-BF14E1A5-A384-43D0-B7B5-EED71D418031

P5875

Q38174180-9E2060AF-22D6-4FFB-9003-CCF6F994E6D8

P698

Q38174180-6991AF54-8636-4BB2-913F-8AA5D9C197F5

P921

Q38174180-637A292F-9AEF-41BA-8870-B10A87894148

Q38174180-6A4A6D7F-87B0-4978-8514-B450E8D4FFDB

Q38174180-BA3D6999-5A1F-4559-B145-588423637CBB

Q38174180-C6E45C6D-DE15-4441-953C-9E1F65800833

P932

Q38174180-58CA57D3-3912-4CF2-97FB-AD786CEFF8EC

P356

1574-6968.12365

P1433

FEMS Microbiology Letters

P1476

Steps towards the synthetic biology of polyketide biosynthesis.

@en

P2093

Matthew Cummings

http://www.w3.org/2001/XMLSchema#string

P275

Creative Commons Attribution 3.0 Unported

P2860

Identification and expression of genes involved in biosynthesis of L-oleandrose and its intermediate L-olivose in the oleandomycin producer Streptomyces antibioticus

Anthracyclines: molecular advances and pharmacologic developments in antitumor activity and cardiotoxicity

Carrier protein structure and recognition in polyketide and nonribosomal peptide biosynthesis.

Traceless protein splicing utilizing evolved split inteins.

Multiple genetic modifications of the erythromycin polyketide synthase to produce a library of novel "unnatural" natural products.

Construction of desosamine containing polyketide libraries using a glycosyltransferase with broad substrate specificity.

Expanding the scope of aromatic polyketides by combinatorial biosynthesis.

Biosynthesis of complex polyketides in a metabolically engineered strain of E. coli.

Interspecies complementation in Saccharopolyspora erythraea : elucidation of the function of oleP1, oleG1 and oleG2 from the oleandomycin biosynthetic gene cluster of Streptomyces antibioticus and generation of new erythromycin derivatives.

Tuning genetic control through promoter engineering

P304

116-125

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/1574-6968.12365

http://www.w3.org/2001/XMLSchema#string

P433

2

http://www.w3.org/2001/XMLSchema#string

P478

351

http://www.w3.org/2001/XMLSchema#string

P50

Rainer Breitling

P577

2014-01-07T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

2014-02-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

259488848

http://www.w3.org/2001/XMLSchema#string

P698

24372666

http://www.w3.org/2001/XMLSchema#string

P921

polycyclic compound

biomedical investigative technique

synthetic biology

P932

4237116

http://www.w3.org/2001/XMLSchema#string