Literature DB >> 11150618

The commercial production of chemicals using pathway engineering.

G Chotani1, T Dodge, A Hsu, M Kumar, R LaDuca, D Trimbur, W Weyler, K Sanford.   

Abstract

Integration of metabolic pathway engineering and fermentation production technologies is necessary for the successful commercial production of chemicals. The 'toolbox' to do pathway engineering is ever expanding to enable mining of biodiversity, to maximize productivity, enhance carbon efficiency, improve product purity, expand product lines, and broaden markets. Functional genomics, proteomics, fluxomics, and physiomics are complementary to pathway engineering, and their successful applications are bound to multiply product turnover per cell, channel carbon efficiently, shrink the size of factories (i.e., reduce steel in the ground), and minimize product development cycle times to bring products to market.

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Year:  2000        PMID: 11150618     DOI: 10.1016/s0167-4838(00)00234-x

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  29 in total

1.  Genetic changes to optimize carbon partitioning between ethanol and biosynthesis in ethanologenic Escherichia coli.

Authors:  S A Underwood; S Zhou; T B Causey; L P Yomano; K T Shanmugam; L O Ingram
Journal:  Appl Environ Microbiol       Date:  2002-12       Impact factor: 4.792

Review 2.  Strain improvement for fermentation and biocatalysis processes by genetic engineering technology.

Authors:  Shu-Jen Chiang
Journal:  J Ind Microbiol Biotechnol       Date:  2004-04-27       Impact factor: 3.346

3.  Functional replacement of the Escherichia coli D-(-)-lactate dehydrogenase gene (ldhA) with the L-(+)-lactate dehydrogenase gene (ldhL) from Pediococcus acidilactici.

Authors:  Shengde Zhou; K T Shanmugam; L O Ingram
Journal:  Appl Environ Microbiol       Date:  2003-04       Impact factor: 4.792

4.  Enhanced trehalose production improves growth of Escherichia coli under osmotic stress.

Authors:  J E Purvis; L P Yomano; L O Ingram
Journal:  Appl Environ Microbiol       Date:  2005-07       Impact factor: 4.792

5.  Using chemobiosynthesis and synthetic mini-polyketide synthases to produce pharmaceutical intermediates in Escherichia coli.

Authors:  Hugo G Menzella; John R Carney; Yong Li; Daniel V Santi
Journal:  Appl Environ Microbiol       Date:  2010-06-11       Impact factor: 4.792

6.  Identification and characterization of coenzyme B12-dependent glycerol dehydratase- and diol dehydratase-encoding genes from metagenomic DNA libraries derived from enrichment cultures.

Authors:  Anja Knietsch; Susanne Bowien; Gregg Whited; Gerhard Gottschalk; Rolf Daniel
Journal:  Appl Environ Microbiol       Date:  2003-06       Impact factor: 4.792

7.  Engineering the metabolism of Escherichia coli W3110 for the conversion of sugar to redox-neutral and oxidized products: homoacetate production.

Authors:  T B Causey; S Zhou; K T Shanmugam; L O Ingram
Journal:  Proc Natl Acad Sci U S A       Date:  2003-01-29       Impact factor: 11.205

8.  Production of optically pure D-lactic acid in mineral salts medium by metabolically engineered Escherichia coli W3110.

Authors:  Shengde Zhou; T B Causey; A Hasona; K T Shanmugam; L O Ingram
Journal:  Appl Environ Microbiol       Date:  2003-01       Impact factor: 4.792

9.  Microbial production and applications of 1,2-propanediol.

Authors:  R K Saxena; Pinki Anand; Saurabh Saran; Jasmine Isar; Lata Agarwal
Journal:  Indian J Microbiol       Date:  2010-03-09       Impact factor: 2.461

10.  Lack of protective osmolytes limits final cell density and volumetric productivity of ethanologenic Escherichia coli KO11 during xylose fermentation.

Authors:  S A Underwood; M L Buszko; K T Shanmugam; L O Ingram
Journal:  Appl Environ Microbiol       Date:  2004-05       Impact factor: 4.792

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