Login / Signup

Identification of RoCYP01 (CYP716A155) enables construction of engineered yeast for high-yield production of betulinic acid.

Jiajian HuangWenlong ZhaTianyue AnHua DongYing HuangDong WangRongmin YuLixin DuanXueli ZhangReuben J PetersZhubo DaiJiachen Zi
Published in: Applied microbiology and biotechnology (2019)
Betulinic acid (BA) and its derivatives possess potent pharmacological activity against cancer and HIV. As with many phytochemicals, access to BA is limited by the requirement for laborious extraction from plant biomass where it is found in low amounts. This might be alleviated by metabolically engineering production of BA into an industrially relevant microbe such as Saccharomyces cerevisiae (yeast), which requires complete elucidation of the corresponding biosynthetic pathway. However, while cytochrome P450 enzymes (CYPs) that can oxidize lupeol into BA have been previously identified from the CYP716A subfamily, these generally do not seem to be specific to such biosynthesis and, in any case, have not been shown to enable high-yielding metabolic engineering. Here RoCYP01 (CYP716A155) was identified from the BA-producing plant Rosmarinus officinalis (rosemary) and demonstrated to effectively convert lupeol into BA, with strong correlation of its expression and BA accumulation. This was further utilized to construct a yeast strain that yields > 1 g/L of BA, providing a viable route for biotechnological production of this valuable triterpenoid.
Keyphrases
  • saccharomyces cerevisiae
  • cell wall
  • poor prognosis
  • human immunodeficiency virus
  • squamous cell carcinoma
  • hiv aids
  • papillary thyroid
  • transcription factor
  • young adults
  • long non coding rna