Germacradienol/geosmin synthase
WebAug 15, 2024 · The geosmin synthase of Streptomyces coelicolor A3(2) is a Mg 2+-dependent bifunctional enzyme. The N-terminal domain of the protein converts FPP to germacradienol, while the C-terminal domain catalyzes the transformation of germacradienol to geosmin (Jiang et al. 2006; Jiang and Cane 2008). WebApr 1, 1999 · germacradienol synthase Alternative Name(s) germacradienol/germacrene-D synthase: Reaction catalysed (2E,6E)-farnesyl diphosphate + H2O => (1E,4S,5E,7R) …
Germacradienol/geosmin synthase
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WebGermacradienol/geosmin Synthase (Gene symbol: SCO6073) Chemicals and Non-standard biopolymers (4 molecules) 1. 3. MAGNESIUM ION. 2. 1. ALENDRONATE * Click molecule labels to explore molecular sequence information. Citing MMDB. Madej T, Lanczycki CJ, Zhang D, Thiessen PA, Geer RC, Marchler-Bauer A, Bryant SH. Webthe Germacradienol/Geosmin Synthase David E. Cane, Xiaofei He, Seiji Kobayashi, Satoshi O¯ mura, Haruo Ikeda This paper is submitted in honor of the late Professor Kenneth L. Rinehart, a pioneer in
Webdiphosphate (FPP) to geosmin via germacradienol (Fig.1) and elucidated one of the terpene metabolite pathways in Streptomyces [16, 17]. We recently isolated a sesquiterpene synthase named spterp13 from Streptomyces peucetius ATCC 27952; this was characterized as a germacradienol synthase that catalyzed the Mg2+-dependent … http://www.reeis.usda.gov/web/crisprojectpages/0233665-relationship-of-geosmin-biosynthesis-to-plant-growth-crop-production-and-food-quality-in-beta-vulgaris.html
WebGermacradienol C15H26O CID 16667385 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities ... WebBegin bi-directional selection for geosmin levels in this population. Specific Aim 4. Use genetic information from bacterial, fungal, and liverwort Germacradienol-geosmin Synthase sequence data and sequence information available from sugarbeet to identify if beet possesses a version of this gene.
WebExternal links. Germacradienol+synthase at the US National Library of Medicine Medical Subject Headings (MeSH)
Web开馆时间：周一至周日7:00-22:30 周五 7:00-12:00; 我的图书馆 tidewater bariatrics chesapeakeWebJul 1, 2024 · Germacradienol demonstrated multiple biological activities, including broad antimicrobial activities with MIC values ranging from 12.5 to 25.0 μg/mL and cytotoxic … tidewater bass club delawareWebApr 21, 2024 · Incubation of this germacradienol/geosmin synthase with [1,1-(2)H2] FPP (2a) gave geosmin-d1 (1a), as predicted. When recombinant GeoA from either S. avermitilis or S. coelicolor A3(2) was ... the majority of venues are privately ownedGeosmin synthase or germacradienol-geosmin synthase designates a class of bifunctional enzymes (EC 4.1.99.16) that catalyze the conversion of farnesyl diphosphate (FPP) to geosmin, a volatile organic compound known for its earthy smell. The N-terminal half of the protein catalyzes the conversion of farnesyl diphosphate to germacradienol and germacrene D, followed by the C-terminal-mediated … the majority of u.s. children live inWebJun 1, 2006 · Incubation of recombinant germacradienol synthase, encoded by the SCO6073 (SC9B1.20) gene of the Gram-positive soil bacterium Streptomyces coelicolor, … the majority of 后面用单数还是复数WebJul 28, 2024 · For the accurate and sensitive quantitation of the off-flavor compound geosmin, particularly in complex matrices, a stable isotopologue as internal standard is highly advantageous. In this work, we present a versatile synthetic strategy leading from (4a R )-1,4a-dimethyl-4,4a,5,6,7,8-hexahydronaphthalen-2(3 H )-one to tri-deuterated ... the majority of 后面加单数还是复数Webgermacradienol seems to be the committed step in the formation of geosmin, the characteristic odoriferous constituent of Strepto-myces species. secondary … the majority of 例文