Biosynthesis and Heterologous Production of Vioprolides: Rational Biosynthetic Engineering and Unprecedented 4-Methylazetidine-carboxylic Acid Formation

被引:66
作者
Yan, Fu [1 ,2 ]
Auerbach, David [1 ,2 ]
Chai, Yi [1 ,2 ]
Keller, Lena [1 ,2 ]
Tu, Qiang [1 ,2 ]
Huettel, Stephan [3 ]
Glemser, Amelie [3 ]
Grab, Hanusch A. [4 ]
Bach, Thorsten [4 ]
Zhang, Youming [5 ]
Mueller, Rolf [1 ,2 ]
机构
[1] Saarland Univ, Helmholtz Ctr Infect Res, Helmholtz Inst Pharmaceut Res Saarland HIPS, Campus Bldg E8-1, D-66123 Saarbrucken, Germany
[2] Saarland Univ, Dept Pharm, Campus Bldg E8-1, D-66123 Saarbrucken, Germany
[3] Helmholtz Ctr Infect Res, Dept Microbial Drugs, Braunschweig, Germany
[4] Tech Univ Munich, Lehrstuhl Organ Chem 1, Lichtenbergstr 4, D-85747 Garching, Germany
[5] Shandong Univ, Sch Life Sci, State Key Lab Microbial Technol, Helmholtz Joint Inst Biotechnol, Qingdao, Peoples R China
关键词
azetidine; biosynthesis; heterologous expression; natural products; vioprolide; GENE-CLUSTER; AZETIDINE-2-CARBOXYLIC ACID; NATURAL-PRODUCTS; EXPRESSION; METHYLATION; ANTIBIOTICS; METHYLTRANSFERASE; PHYTOSIDEROPHORES; GLIDOBACTIN; EPOTHILONES;
D O I
10.1002/anie.201802479
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Vioprolides are a promising class of anticancer and antifungal lead compounds produced by the myxobacterium Cystobacter violaceus Cbvi35. Previously nothing had been reported about their biosynthesis, including the origin of the unusual 4-methylazetidinecarboxylic acid (MAZ) moiety. We describe the vioprolide biosynthetic gene cluster and solve the production obstacle by expression in three heterologous hosts. Starting from unstable production in the wild type at the single-digit mgL(-1) scale, we developed a stable host that eventually allowed for yields of up to half a gram per liter in fermenters. Gene inactivations coupled with isotope feeding studies identified an S-adenosylmethionine (SAM)-dependent enzyme and a methyltransferase as being responsible for the generation of the MAZ building block by a proposed mechanism unprecedented in bacteria. Furthermore, nonnatural vioprolide derivatives were generated via rational genetic engineering.
引用
收藏
页码:8754 / 8759
页数:6
相关论文
共 48 条
[1]
Initial characterization of Fom3 from Streptomyces wedmorensis: The methyltransferase in fosfomycin biosynthesis [J].
Allen, Kylie D. ;
Wang, Susan C. .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2014, 543 :67-73
[2]
Mechanistic and functional insights into fatty acid activation in Mycobacterium tuberculosis [J].
Arora, Pooja ;
Goyal, Aneesh ;
Natarajan, Vivek T. ;
Rajakumara, Eerappa ;
Verma, Priyanka ;
Gupta, Radhika ;
Yousuf, Malikmohamed ;
Trivedi, Omita A. ;
Mohanty, Debasisa ;
Tyagi, Anil ;
Sankaranarayanan, Rajan ;
Gokhale, Rajesh S. .
NATURE CHEMICAL BIOLOGY, 2009, 5 (03) :166-173
[3]
Heterologous Production and Yield Improvement of Epothilones in Burkholderiales Strain DSM 7029 [J].
Bian, Xiaoying ;
Tang, Biao ;
Yu, Yucong ;
Tu, Qiang ;
Gross, Frank ;
Wang, Hailong ;
Li, Aiying ;
Shen, Yuemao ;
Li, Yue-zhong ;
Stewart, A. Francis ;
Zhao, Guoping ;
Ding, Xiaoming ;
Mueller, Rolf ;
Zhang, Youming .
ACS CHEMICAL BIOLOGY, 2017, 12 (07) :1805-1812
[4]
Heterologous Production of Glidobactins/Luminmycins in Escherichia coli Nissle Containing the Glidobactin Biosynthetic Gene Cluster from Burkholderia DSM7029 [J].
Bian, Xiaoying ;
Huang, Fan ;
Wang, Hailong ;
Klefisch, Thorsten ;
Mueller, Rolf ;
Zhang, Youming .
CHEMBIOCHEM, 2014, 15 (15) :2221-2224
[5]
Efficient methylation of C2 in L-tryptophan by the cobalamin-dependent radical S-adenosylmethionine methylase TsrM requires an unmodified N1 amine [J].
Blaszczyk, Anthony J. ;
Wang, Bo ;
Silakov, Alexey ;
Ho, Jackson V. ;
Booker, Squire J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2017, 292 (37) :15456-15467
[6]
antiSMASH 2.0-a versatile platform for genome mining of secondary metabolite producers [J].
Blin, Kai ;
Medema, Marnix H. ;
Kazempour, Daniyal ;
Fischbach, Michael A. ;
Breitling, Rainer ;
Takano, Eriko ;
Weber, Tilmann .
NUCLEIC ACIDS RESEARCH, 2013, 41 (W1) :W204-W212
[7]
Heterologous Expression and Genetic Engineering of the Tubulysin Biosynthetic Gene Cluster Using Red/ET Recombineering and Inactivation Mutagenesis [J].
Chai, Yi ;
Shan, Shiping ;
Weissman, Kira J. ;
Hu, Shengbiao ;
Zhang, Youming ;
Mueller, Rolf .
CHEMISTRY & BIOLOGY, 2012, 19 (03) :361-371
[8]
Characterization of the Polyoxin Biosynthetic Gene Cluster from Streptomyces cacaoi and Engineered Production of Polyoxin H [J].
Chen, Wenqing ;
Huang, Tingting ;
He, Xinyi ;
Meng, Qingqing ;
You, Delin ;
Bai, Linquan ;
Li, Jialiang ;
Wu, Mingxuan ;
Li, Rui ;
Xie, Zhoujie ;
Zhou, Huchen ;
Zhou, Xiufen ;
Tan, Huarong ;
Deng, Zixin .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (16) :10627-10638
[9]
Isolation, X-ray crystallography, and computational studies of calydaphninone, a new alkaloid from Daphniphyllum calycillum [J].
Di, Ying-Tong ;
He, Hong-Ping ;
Wang, Yun-Song ;
Li, Liang-Bo ;
Lu, Yang ;
Gong, Jian-Bo ;
Fang, Xin ;
Kong, Ning-Chuan ;
Li, Shun-Lin ;
Zhu, Hua-Jie ;
Hao, Xiao-Jiang .
ORGANIC LETTERS, 2007, 9 (07) :1355-1358
[10]
Higher-order chromatin domains link eQTLs with the expression of far-away genes [J].
Duggal, Geet ;
Wang, Hao ;
Kingsford, Carl .
NUCLEIC ACIDS RESEARCH, 2014, 42 (01) :87-96