Cloning, expression, and characterization of epi-cedrol synthase, a sesquiterpene cyclase from Artemisia annua L

被引:98
|
作者
Mercke, P
Crock, J
Croteau, R
Brodelius, PE
机构
[1] Univ Kalmar, Dept Nat Sci, S-39129 Kalmar, Sweden
[2] Washington State Univ, Inst Biol Chem, Pullman, WA 99164 USA
[3] Univ Lund, Dept Plant Biochem, S-22100 Lund, Sweden
关键词
epi-cedrol synthase cDNA; sesquiterpene cyclase; monoterpene cyclase; bacterial expression; Artemisia annua;
D O I
10.1006/abbi.1999.1358
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sesquiterpene cyclases (synthases) catalyze the conversion of the isoprenoid intermediate farnesyl diphosphate to various sesquiterpene structural types. In plants, many sesquiterpenes are produced as defensive chemicals (phytoalexins) or mediators of chemical communication (i.e., pollinator attractants). A number of sesquiterpene synthases are present in Artemisia annua L. (annual wormwood). We have isolated a cDNA clone encoding one of these, epi-cedrol synthase. This clone contains a 1641-bp open reading frame coding for 547 amino acids (63.5 kDa), a 38-bp 5'-untranslated end, and a 272-bp 3'-untranslated sequence. The deduced amino acid sequence was 32 to 43% identical with the sequences of other known sesquiterpene cyclases from angiosperms. When expressed in Escherichia coli, the recombinant enzyme catalyzed the formation of both olefinic (3%) and oxygenated (97%) sesquiterpenes from farnesyl diphosphate. GC-MS analysis identified the olefins as alpha-cedrene (57% of the olefins), beta-cedrene (13%), (E)-beta-farnesene (5%), alpha-acoradiene (1%), (E)-alpha-bisabolene (8%), and three unknown olefins (16%) and the oxygenated sesquiterpenes (97% of total sesquiterpene generated, exclusive of farnesol and nerolidol) as cedrol (4%) and epi-cedrol (96%). epi-Cedrol synthase was not active with geranylgeranyl diphosphate as substrate, whereas geranyl diphosphate was converted to monoterpenes by the recombinant enzyme at a rate of about 15% of that observed with farnesyl diphosphate as substrate. The monoterpene olefin products are limonene (45%), terpinolene (42%), gamma-terpinene (8%), myrcene (5%), and alpha-terpinene (2%); a small amount of the monoterpene alcohol terpinen-4-ol is also produced. The pH optimum for the recombinant enzyme is 8.5-9.0 (with farnesyl diphosphate as substrate) and the IT, values for farnesyl diphosphate are 0.4 and 1.3 mu M at pH 7.0 and 9.0, respectively. The K-m for Mg2+ is 80 mu M at pH 7.0 and 9.0. (C) 1999 Academic Press.
引用
收藏
页码:213 / 222
页数:10
相关论文
共 50 条
  • [1] Enhancing epi-cedrol production in Escherichia coli by fusion expression of farnesyl pyrophosphate synthase and epi-cedrol synthase
    Navale, Govinda R.
    Sharma, Poojadevi
    Said, Madhukar S.
    Ramkumar, Sudha
    Dharne, Mahesh S.
    Thulasiram, H., V
    Shinde, Sandip S.
    ENGINEERING IN LIFE SCIENCES, 2019, 19 (09): : 606 - 616
  • [2] cDNA isolation, characterization and bacterial expression of a sesquiterpene synthase from artemisia annua
    Hua, L
    Matsuda, SPT
    FASEB JOURNAL, 1999, 13 (07): : A1553 - A1553
  • [3] Cloning, E-coli expression and molecular analysis of a novel sesquiterpene synthase gene from Artemisia annua
    Liu, Y
    Ye, HC
    Li, GF
    ACTA BOTANICA SINICA, 2002, 44 (12): : 1450 - 1455
  • [4] In vitro regeneration and transient expression of recombinant sesquiterpene cyclase (SQC) in Artemisia annua L.
    Mirzaee, H.
    Sharafi, A.
    Sohi, H. Hashemi
    SOUTH AFRICAN JOURNAL OF BOTANY, 2016, 104 : 225 - 231
  • [5] Cloning and functional characterization of a β-pinene synthase from Artemisia annua that shows a circadian pattern of expression
    Lu, S
    Xu, R
    Jia, JW
    Pang, JH
    Matsuda, SPT
    Chen, XY
    PLANT PHYSIOLOGY, 2002, 130 (01) : 477 - 486
  • [6] Cloning and molecular analysis of two new sesquiterpene cyclases from Artemisia annua L.
    Van Geldre, E
    De Pauw, I
    Inzé, D
    Van Montagu, M
    Van den Eeckhout, E
    PLANT SCIENCE, 2000, 158 (1-2) : 163 - 171
  • [7] Cloning and Characterization of a Carotenoid Cleavage Dioxygenase from Artemisia Annua L.
    Liu, Shuoqian
    Tian, Na
    Liu, Zhonghua
    Huang, Jianan
    Li, Juan
    MECHANICAL ENGINEERING AND MATERIALS SCIENCE, 2012, 108 : 274 - 281
  • [8] Functional expression and characterization of sesquiterpene synthases from Artemisia annua L. using transient expression system in Nicotiana benthamiana
    Kanagarajan, Selvaraju
    Muthusamy, Saraladevi
    Gliszczynska, Anna
    Lundgren, Anneli
    Brodelius, Peter E.
    PLANT CELL REPORTS, 2012, 31 (07) : 1309 - 1319
  • [9] Functional expression and characterization of sesquiterpene synthases from Artemisia annua L. using transient expression system in Nicotiana benthamiana
    Selvaraju Kanagarajan
    Saraladevi Muthusamy
    Anna Gliszczyńska
    Anneli Lundgren
    Peter E. Brodelius
    Plant Cell Reports, 2012, 31 : 1309 - 1319
  • [10] Cloning, expression, and immunological characterization of two novel profilins from Artemisia annua
    Hu, Qiao-Li
    Zhu, Li-Xiang
    Xu, Zhi-Qiang
    Pan, Chen
    Zhong, Qiu-Min
    Sun, Jin-Lyu
    Wei, Ji-Fu
    CHINESE MEDICAL JOURNAL, 2021, 134 (10) : 1224 - 1226