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3SDU

Structure of a three-domain sesquiterpene synthase: a prospective target for advanced biofuels production

Summary for 3SDU
Entry DOI10.2210/pdb3sdu/pdb
Related3SAE 3SDQ 3SDR 3SDT 3SDV
DescriptorAlpha-bisabolene synthase, CHLORIDE ION, MAGNESIUM ION, ... (5 entities in total)
Functional Keywordslyase, terpene synthase
Biological sourceAbies grandis (grand fir,lowland fir,lowland white fir,silver fir,white fir,yellow fir)
Cellular locationCytoplasm (Probable): O81086
Total number of polymer chains1
Total formula weight94293.78
Authors
McAndrew, R.P.,Peralta-Yahya, P.P.,DeGiovanni, A.,Pereira, J.H.,Hadi, M.Z.,Keasling, J.D.,Adams, P.D. (deposition date: 2011-06-09, release date: 2011-12-14, Last modification date: 2024-02-28)
Primary citationMcAndrew, R.P.,Peralta-Yahya, P.P.,DeGiovanni, A.,Pereira, J.H.,Hadi, M.Z.,Keasling, J.D.,Adams, P.D.
Structure of a three-domain sesquiterpene synthase: a prospective target for advanced biofuels production.
Structure, 19:1876-1884, 2011
Cited by
PubMed Abstract: The sesquiterpene bisabolene was recently identified as a biosynthetic precursor to bisabolane, an advanced biofuel with physicochemical properties similar to those of D2 diesel. High-titer microbial bisabolene production was achieved using Abies grandis α-bisabolene synthase (AgBIS). Here, we report the structure of AgBIS, a three-domain plant sesquiterpene synthase, crystallized in its apo form and bound to five different inhibitors. Structural and biochemical characterization of the AgBIS terpene synthase Class I active site leads us to propose a catalytic mechanism for the cyclization of farnesyl diphosphate into bisabolene via a bisabolyl cation intermediate. Further, we describe the nonfunctional AgBIS Class II active site whose high similarity to bifunctional diterpene synthases makes it an important link in understanding terpene synthase evolution. Practically, the AgBIS crystal structure is important in future protein engineering efforts to increase the microbial production of bisabolene.
PubMed: 22153510
DOI: 10.1016/j.str.2011.09.013
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.89 Å)
Structure validation

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