Reconstitution of biosynthetic machinery for the synthesis of the highly elaborated indole diterpene penitrem. - Wikidata - wikimedia - TriplyDB

Reconstitution of biosynthetic machinery for the synthesis of the highly elaborated indole diterpene penitrem.

Reconstitution of biosynthetic machinery for the synthesis of the highly elaborated indole diterpene penitrem.

http://www.wikidata.org/entity/Q41127959

about

Molecular Cloning and Functional Analysis of Gene Clusters for the Biosynthesis of Indole-Diterpenes in Penicillium crustosum and P. janthinellum.Total Synthesis of (-)-Nodulisporic Acid D.Biosynthesis of fungal meroterpenoids.Oxidative Cyclization in Natural Product Biosynthesis Influence of Environmental Factors on the Production of Penitrems A-F by Penicillium crustosum.Discovery of Unclustered Fungal Indole Diterpene Biosynthetic Pathways through Combinatorial Pathway Reassembly in Engineered Yeast.Subcellular localization of aphidicolin biosynthetic enzymes heterologously expressed in Aspergillus oryzae.Biosynthetic Machinery of Diterpene Pleuromutilin Isolated from Basidiomycete Fungi.Expansion of chemical space for natural products by uncommon P450 reactions.Reconstitution of biosynthetic machinery of fungal polyketides: unexpected oxidations of biosynthetic intermediates by expression host.Safety of the fungal workhorses of industrial biotechnology: update on the mycotoxin and secondary metabolite potential of Aspergillus niger, Aspergillus oryzae, and Trichoderma reesei Hot off the press

P2860

Q35715717-329E22F7-2AE3-4EE2-8364-8A9F18A36049 Q35775905-5EC51D0C-4F26-4C5F-ADD7-927FA8EB46E1 Q38615304-2B3C7C90-EF93-4959-95AB-DAC83E53BF35 Q39034361-E0868796-4A18-4AA8-98F5-D54BF0CA60A3 Q41175053-7E5F9E7C-199A-4FF5-96CD-7B414AFE63A4 Q42536079-192E01EA-6F24-41E9-86C8-3EA2AF186FFE Q47298196-BD4699D0-9EA8-4ED9-9E7E-964377FE3C8C Q47780684-DA0A83A6-7502-46B1-9478-DB71AFC4E3E5 Q47996749-CA8EED8E-1EBE-4D0D-B3CA-79332F0B6CDA Q53658011-5F81DED9-5F98-44F9-8577-B84122BB1E7E Q57183197-7EC3375B-5A36-4FE6-9882-3C7489499621 Q58856781-E509726E-DA4C-4473-8A10-387EE899D06A

P2860

Reconstitution of biosynthetic machinery for the synthesis of the highly elaborated indole diterpene penitrem.

http://www.wikidata.org/entity/Q41127959

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Reconstitution of biosynthetic ...... ted indole diterpene penitrem.

@en

type

label

Reconstitution of biosynthetic ...... ted indole diterpene penitrem.

@en

prefLabel

Reconstitution of biosynthetic ...... ted indole diterpene penitrem.

@en

P1433

Q41127959-6567DB92-9A3F-4C0D-8EEF-E3EB0C3D4958

P1476

Q41127959-62D1C38A-170F-47D6-AC79-EC6CC6A3DB0E

P2093

Q41127959-58752750-FB0E-40AA-8EC0-AE566CC0347A

Q41127959-955777F6-F953-4EA9-803A-ECDFB3B21732

Q41127959-99810D0D-44E4-4D07-872B-ADA3E96BCDE7

Q41127959-A45BF963-8F3C-47FC-949A-CE305E044987

Q41127959-A943A073-CCB8-488D-94A1-4B44087D6E7E

Q41127959-D06D3F1F-D483-41A3-8CFD-CA2DADE56943

P2860

Q41127959-00C20706-4E02-4434-A431-D820F537DC3B

Q41127959-074C4D44-59F4-4170-9C20-239F7477EFCD

Q41127959-13DCC4E8-37EF-44CC-BBE7-1E76C2581D5A

Q41127959-2650156C-3DA4-408E-AD30-F230C418C57D

Q41127959-2AF92A37-3984-47F9-A8B5-CB30A9AAEFFB

Q41127959-2EFC3E1E-0721-4905-997E-26190A24A87B

Q41127959-57BF98CF-52FC-4544-9C4D-CDF79F878AF8

Q41127959-594C0362-350D-4DA5-971F-F0D0170581E9

Q41127959-62C289BD-A857-4D99-8DB4-FA37D89F3E22

Q41127959-6586454D-BC9A-47CE-A74C-BBFD7C978F7A

P304

Q41127959-3B13604C-D143-4EA8-B5D5-A05A748E4B89

P31

Q41127959-CB64D7C9-C1A3-46D0-8B18-59DB2CA2C722

P356

Q41127959-4617EB86-304D-444A-9CFE-46EB6349A4A8

P407

Q41127959-55012FB9-E727-4B9F-B3B1-5932AC467476

P433

Q41127959-784E2FB9-AEE8-4079-A54A-8E1291F5985E

P478

Q41127959-F2D5F69A-EC60-413B-8584-758ED996A726

P50

Q41127959-004018C4-8638-43FC-9620-E24310A36C1C

Q41127959-1F06BC40-F59D-4F54-AE93-15765403B652

Q41127959-F5B53B55-8B49-4A59-B64D-527DF230699B

P577

Q41127959-58E7F9F2-91E7-44C6-B1C3-775428B4E571

P698

Q41127959-4B67C19C-C816-4CBD-B2C3-F9D33DE22F58

P356

P1433

Angewandte Chemie International Edition

P1476

Reconstitution of biosynthetic ...... ated indole diterpene penitrem

@en

P2093

Chengwei Liu

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

Hideaki Oikawa

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

Hideyuki Suzuki

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

Jun Ishikawa

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

Koichi Tagami

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

Tomoyuki Matsumoto

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

P2860

The structural basis of cephalosporin formation in a mononuclear ferrous enzyme

Structure of a cephalosporin synthase

Identification and nomenclature of the genus Penicillium

Molecular cloning and genetic analysis of an indole-diterpene gene cluster from Penicillium paxilli.

Unusual acetylation-elimination in the formation of tetronate antibiotics.

Defining paxilline biosynthesis in Penicillium paxilli: functional characterization of two cytochrome P450 monooxygenases.

The genetic basis for indole-diterpene chemical diversity in filamentous fungi.

A gene cluster containing two fungal polyketide synthases encodes the biosynthetic pathway for a polyketide, asperfuranone, in Aspergillus nidulans

Identification of two aflatrem biosynthesis gene loci in Aspergillus flavus and metabolic engineering of Penicillium paxilli to elucidate their function.

Total biosynthesis of diterpene aphidicolin, a specific inhibitor of DNA polymerase α: heterologous expression of four biosynthetic genes in Aspergillus oryzae.

P304

5748-5752

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

P31

scholarly article

P356

10.1002/ANIE.201501072

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

P407

P433

19

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

P478

54

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

P50

P577

2015-04-01T00:00:00Z

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

P698

25831977

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