Toward biosynthetic design and implementation of Escherichia coli-derived paclitaxel and other heterologous polyisoprene compounds.

Abstract:

:Escherichia coli offers unparalleled engineering capacity in the context of heterologous natural product biosynthesis. However, as with other heterologous hosts, cellular metabolism must be designed or redesigned to support final compound formation. This task is at once complicated and aided by the fact that the cell does not natively produce an abundance of natural products. As a result, the metabolic engineer avoids complicated interactions with native pathways closely associated with the outcome of interest, but this convenience is tempered by the need to implement the required metabolism to allow functional biosynthesis. This review focuses on engineering E. coli for the purpose of polyisoprene formation, as it is related to isoprenoid compounds currently being pursued through a heterologous approach. In particular, the review features the compound paclitaxel and early efforts to design and overproduce intermediates through E. coli.

journal_name

Appl Environ Microbiol

authors

Jiang M,Stephanopoulos G,Pfeifer BA

doi

10.1128/AEM.07391-11

subject

Has Abstract

pub_date

2012-04-01 00:00:00

pages

2497-504

issue

8

eissn

0099-2240

issn

1098-5336

pii

AEM.07391-11

journal_volume

78

pub_type

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