The ultimate goal of this project is to understand at the molecular level how the oxirane group of fosfomycin, the cyclohexene moiety of spinosyn A, and the annelated oligocyclobutane ring system of ladderane lipids are biosynthesized. Fosfomycin is a clinically useful antibiotic and chemically versatile synthon in the research and development of new therapeutics largely on account of its reactive epoxide ring. Spinosyn A is an environmentally "green" commercial insecticide with activity against insects detrimental to both human health and harvested plants. Ladderane lipids are a necessary component of the intracytoplasmic compartment of bacteria responsible for anaerobic ammonia oxidation (anammox). This process is employed in the bioremediation of nitrogen-contaminated wastewater. Therefore, the continued development of these compounds in the interest of public health requires a more complete understanding of the chemistry underlying their biosyntheses. To achieve these goals, detailed enzyme analysis will be coupled with chemical synthetic methods to develop mechanistic probes specific to the unique challenges each system presents. The mononuclear non-heme iron enzyme HppE, which is responsible for the oxirane of fosfomycin, will be investigated using a combination of 18O kinetic isotope effects, radical clock probes, designer substrate analogues, and spectroscopic methods. These techniques will be used to characterize the radical intermediates of HppE catalysis and to identify the reactive iron-oxygen species (FeIII-OO? versus FeIV=O) responsible for their formation. The enzyme SpnF, which catalyzes the [4+2]-cycloaddition responsible for the construction of the cyclohexene ring of spinosyn A, will be investigated to verify whether it is indeed the first- confirmed natural Diels-Alderase. This hypothesis will be tested using secondary deuterium kinetic isotope effects and further characterized via thermodynamic and kinetic study of the cycloaddition reaction. The biosynthetic pathway of ladderanes is believed to involve polyunsaturated fatty acids with cyclization proceeding through B12-dependent radical SAM chemistry. Therefore, the putative biosynthetic gene cluster from Kuenenia stutgartiensis will be interrogated by reconstituting the ful pathway in vitro using chemo- enzymatically prepared substrates so as to characterize the key cyclization reactions. These studies will significantly enhance our understanding of the diverse chemistry and enzymology (non-heme iron-dependent oxidases, B12-dependent radical SAM enzymes, Diels-Alderases) of biological cyclization reactions, which can be exploited in future combinatorial biosynthetic endeavors to generate novel and structurally diverse compounds with therapeutic potential.

Public Health Relevance

The ring containing compounds at the center of the proposal have established relevance with regard to public health in terms of antimicrobial development (fosfomycin), the control of insect pests (spinosyn A) and the bioremediation of nitrogen-contaminated wastewater (the ladderanes). Nevertheless, the biochemistry by which they are produced cannot be understood in terms of currently recognized paradigms of enzyme catalysis. This gap in understanding will be addressed by the proposal such that these and related compounds may be further developed for biomedical and biotechnological purposes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM040541-23
Application #
8372548
Study Section
Special Emphasis Panel (ZRG1-BCMB-U (02))
Program Officer
Anderson, Vernon
Project Start
1989-04-01
Project End
2016-06-30
Budget Start
2012-07-01
Budget End
2013-06-30
Support Year
23
Fiscal Year
2012
Total Cost
$332,147
Indirect Cost
$112,147
Name
University of Texas Austin
Department
None
Type
Schools of Pharmacy
DUNS #
170230239
City
Austin
State
TX
Country
United States
Zip Code
78712
Kim, Hak Joong; Choi, Sei-hyun; Jeon, Byung-sun et al. (2014) Chemoenzymatic synthesis of spinosyn A. Angew Chem Int Ed Engl 53:13553-7
Huang, Hui; Chang, Wei-Chen; Lin, Geng-Min et al. (2014) Mechanistic consequences of chiral radical clock probes: analysis of the mononuclear non-heme iron enzyme HppE with 2-hydroxy-3-methylenecyclopropyl radical clock substrates. J Am Chem Soc 136:2944-7
Chang, Wei-chen; Mansoorabadi, Steven O; Liu, Hung-wen (2013) Reaction of HppE with substrate analogues: evidence for carbon-phosphorus bond cleavage by a carbocation rearrangement. J Am Chem Soc 135:8153-6
Chang, Wei-chen; Dey, Mishtu; Liu, Pinghua et al. (2013) Mechanistic studies of an unprecedented enzyme-catalysed 1,2-phosphono-migration reaction. Nature 496:114-8
Wang, Chen; Chang, Wei-chen; Guo, Yisong et al. (2013) Evidence that the fosfomycin-producing epoxidase, HppE, is a non-heme-iron peroxidase. Science 342:991-5
Zhao, Lishan; Chang, Wei-chen; Xiao, Youli et al. (2013) Methylerythritol phosphate pathway of isoprenoid biosynthesis. Annu Rev Biochem 82:497-530
Chang, Wei-chen; Song, Heng; Liu, Hung-wen et al. (2013) Current development in isoprenoid precursor biosynthesis and regulation. Curr Opin Chem Biol 17:571-9
Calveras, Jordi; Thibodeaux, Christopher J; Mansoorabadi, Steven O et al. (2012) Stereochemical studies of the type II isopentenyl diphosphate-dimethylallyl diphosphate isomerase implicate the FMN coenzyme in substrate protonation. Chembiochem 13:42-6
Thibodeaux, Christopher J; Chang, Wei-chen; Liu, Hung-wen (2012) Enzymatic chemistry of cyclopropane, epoxide, and aziridine biosynthesis. Chem Rev 112:1681-709
Kim, Hak Joong; Ruszczycky, Mark W; Liu, Hung-wen (2012) Current developments and challenges in the search for a naturally selected Diels-Alderase. Curr Opin Chem Biol 16:124-31

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