TY - JOUR
T1 - Production of squalene by squalene synthases and their truncated mutants in Escherichia coli
AU - Katabami, Akinori
AU - Li, Ling
AU - Iwasaki, Miki
AU - Furubayashi, Maiko
AU - Saito, Kyoichi
AU - Umeno, Daisuke
N1 - Funding Information:
D.U. is supported by the PRESTO (JST) and the MEXT / JSPS Grant-in-Aid for Scientific Research on Innovative Areas 23108507 . M.F. and M.I are supported by a JSPS fellowship for young scientists. This work is financially supported by the Mishima-Kaiun Memorial Foundation , the Futaba Electronics Memorial Foundation , and the Shorai Foundation for Science and Technology .
Publisher Copyright:
© 2014 The Society for Biotechnology, Japan.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Squalene is a precursor of thousands of bioactive triterpenoids and also has industrial value as a lubricant, health-promoting agent, and/or drop-in biofuel. To establish an efficient Escherichia coli-based system for squalene production, we tested two different squalene synthases and their mutants in combination with precursor pathways. By co-expressing a chimeric mevalonate pathway with human or Thermosynechococcus squalene synthase, E.coli accumulated squalene up to 230mg/L or 55mg/g-DCW in flask culture. We also determined that a significant truncation of squalene synthase at the C-terminus retains partial cellular activity. The squalene-producing strain described herein represents a convenient platform for gene discovery and the construction of the pathway toward natural and non-natural hopanoids/steroids.
AB - Squalene is a precursor of thousands of bioactive triterpenoids and also has industrial value as a lubricant, health-promoting agent, and/or drop-in biofuel. To establish an efficient Escherichia coli-based system for squalene production, we tested two different squalene synthases and their mutants in combination with precursor pathways. By co-expressing a chimeric mevalonate pathway with human or Thermosynechococcus squalene synthase, E.coli accumulated squalene up to 230mg/L or 55mg/g-DCW in flask culture. We also determined that a significant truncation of squalene synthase at the C-terminus retains partial cellular activity. The squalene-producing strain described herein represents a convenient platform for gene discovery and the construction of the pathway toward natural and non-natural hopanoids/steroids.
KW - Bacterial production
KW - Carotenoid
KW - Mevalonate pathway
KW - Squalene synthase
KW - Triterpenoid
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U2 - 10.1016/j.jbiosc.2014.07.013
DO - 10.1016/j.jbiosc.2014.07.013
M3 - Article
C2 - 25282635
AN - SCOPUS:84922575910
SN - 1389-1723
VL - 119
SP - 165
EP - 171
JO - Journal of Bioscience and Bioengineering
JF - Journal of Bioscience and Bioengineering
IS - 2
ER -