Metabolite Profiling Identified Methylerythritol Cyclodiphosphate Efflux as a Limiting Step in Microbial Isoprenoid Production

Isoprenoids are natural products that are all derived from isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). These precursors are synthesized either by the mevalonate (MVA) pathway or the 1-Deoxy-D-Xylulose 5-Phosphate (DXP) pathway. Metabolic engineering of microbes has enabled o...

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Main Authors: Zhou, Kang (Contributor), Zou, Ruiyang (Contributor), Stephanopoulos, Gregory (Contributor), Too, Heng-Phon (Contributor)
Other Authors: Massachusetts Institute of Technology. Department of Chemical Engineering (Contributor), Singapore-MIT Alliance in Research and Technology (SMART) (Contributor)
Format: Article
Language:English
Published: Public Library of Science, 2013-01-30T15:31:44Z.
Subjects:
Online Access:Get fulltext
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100 1 0 |a Zhou, Kang  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Chemical Engineering  |e contributor 
100 1 0 |a Singapore-MIT Alliance in Research and Technology   |q  (SMART)   |e contributor 
100 1 0 |a Zhou, Kang  |e contributor 
100 1 0 |a Zou, Ruiyang  |e contributor 
100 1 0 |a Stephanopoulos, Gregory  |e contributor 
100 1 0 |a Too, Heng-Phon  |e contributor 
700 1 0 |a Zou, Ruiyang  |e author 
700 1 0 |a Stephanopoulos, Gregory  |e author 
700 1 0 |a Too, Heng-Phon  |e author 
245 0 0 |a Metabolite Profiling Identified Methylerythritol Cyclodiphosphate Efflux as a Limiting Step in Microbial Isoprenoid Production 
260 |b Public Library of Science,   |c 2013-01-30T15:31:44Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/76647 
520 |a Isoprenoids are natural products that are all derived from isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). These precursors are synthesized either by the mevalonate (MVA) pathway or the 1-Deoxy-D-Xylulose 5-Phosphate (DXP) pathway. Metabolic engineering of microbes has enabled overproduction of various isoprenoid products from the DXP pathway including lycopene, artemisinic acid, taxadiene and levopimaradiene. To date, there is no method to accurately measure all the DXP metabolic intermediates simultaneously so as to enable the identification of potential flux limiting steps. In this study, a solid phase extraction coupled with ultra performance liquid chromatography mass spectrometry (SPE UPLC-MS) method was developed. This method was used to measure the DXP intermediates in genetically engineered E. coli. Unexpectedly, methylerythritol cyclodiphosphate (MEC) was found to efflux when certain enzymes of the pathway were over-expressed, demonstrating the existence of a novel competing pathway branch in the DXP metabolism. Guided by these findings, ispG was overexpressed and was found to effectively reduce the efflux of MEC inside the cells, resulting in a significant increase in downstream isoprenoid production. This study demonstrated the necessity to quantify metabolites enabling the identification of a hitherto unrecognized pathway and provided useful insights into rational design in metabolic engineering. 
520 |a Singapore-MIT Alliance 
546 |a en_US 
655 7 |a Article 
773 |t PLoS ONE