TY - GEN
T1 - Styrene biosynthesis from glucose by engineered E. Coli
AU - McKenna, Rebekah
AU - Nielsen, David
N1 - Funding Information:
We thank Prof. Bradley Moore (UCSD) and Prof. Kristala Prather (MIT) for their kind gifts. We also thank Tom Colella (ASU) for his skillful technical assistance in GC-MS analysis.
Publisher Copyright:
© 2011 Elsevier Inc. All rights reserved.
PY - 2011
Y1 - 2011
N2 - Styrene is a large volume, commodity petrochemical with diverse commercial applications, including as a monomer building-block for the synthesis of many useful polymers. Here we demonstrate how, through the de novo design and development of a novel metabolic pathway, styrene can alternatively be synthesized from renewable substrates such as glucose. The conversion of endogenously synthesized L-phenylalanine to styrene was achieved by the co-expression of phenylalanine ammonia lyase and trans-cinnamate decarboxylase. Candidate isoenzymes for each step were screened from bacterial, yeast, and plant genetic sources. Finally, over-expression of PAL2 from Arabidopsis thaliana and FDC1 from Saccharomyces cerevisiae (originally classified as ferulate decarboxylase) in an L-phenylalanine over-producing Escherichia coli host led to the accumulation of up to 260 mg/L in shake flask cultures. Achievable titers already approach the styrene toxicity threshold (determined as 300 mg/L). To the best of our knowledge, this is the first report of microbial styrene production from sustainable feedstocks.
AB - Styrene is a large volume, commodity petrochemical with diverse commercial applications, including as a monomer building-block for the synthesis of many useful polymers. Here we demonstrate how, through the de novo design and development of a novel metabolic pathway, styrene can alternatively be synthesized from renewable substrates such as glucose. The conversion of endogenously synthesized L-phenylalanine to styrene was achieved by the co-expression of phenylalanine ammonia lyase and trans-cinnamate decarboxylase. Candidate isoenzymes for each step were screened from bacterial, yeast, and plant genetic sources. Finally, over-expression of PAL2 from Arabidopsis thaliana and FDC1 from Saccharomyces cerevisiae (originally classified as ferulate decarboxylase) in an L-phenylalanine over-producing Escherichia coli host led to the accumulation of up to 260 mg/L in shake flask cultures. Achievable titers already approach the styrene toxicity threshold (determined as 300 mg/L). To the best of our knowledge, this is the first report of microbial styrene production from sustainable feedstocks.
KW - Aromatic
KW - Cinnamic acid
KW - E. coli
KW - L-Phenylalanine
KW - Phenylalanine ammonia lyase
KW - Styrene
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M3 - Conference contribution
AN - SCOPUS:85054588970
SN - 9781618395825
T3 - International Congress on Energy 2011 - Topical Conference at the 2011 AIChE Annual Meeting
SP - 672
EP - 682
BT - International Congress on Energy 2011 - Topical Conference at the 2011 AIChE Annual Meeting
PB - AIChE
T2 - International Congress on Energy 2011 - Topical Conference at the 2011 AIChE Annual Meeting
Y2 - 16 October 2011 through 21 October 2011
ER -