Chemical structure of germicidins A-D | |
Names | |
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IUPAC names
3-Ethyl-4-hydroxy-6-isopropyl-2H-pyran-2-one (germicidin A) 6-(sec-Butyl)-4-hydroxy-3-methyl-2H-pyran-2-one (germicidin B) 6-(sec-Butyl)-3-ethyl-4-hydroxy-2H-pyran-2-one (germicidin C) 4-Hydroxy-6-isopropyl-3-methyl-2H-pyran-2-one (germicidin D) | |
Other names surugapyrone A (Germicidin D) | |
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3D model (JSmol) | |
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CompTox Dashboard (EPA) | |
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Properties | |
Chemical formula | Germicidin A/B - C10H14O3, Germicidin C - C11H16O3, Germicidin D - C9H12O3 |
Molar mass | Germicidin A/B - 182.22g/mol, Germicidin C - 196.25g/mol, Germicidin D - 168.19g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
Germicidins are a groups of natural products arising from Streptomyces species that acts as autoregulatory inhibitor of spore germination. In Streptomyces viriochromogenes, low concentrations (200 pM) inhibit germination of its own arthrospores, and higher concentrations inhibit porcine Na+/K+ -activated ATPase. Inhibitory effects on germination are also observed when germicidin from Streptomyces is applied to Lepidium sativum. Germicidins and other natural products present potential use as pharmaceuticals, and in this case, those with possible antibiotic or antifungal activity.
Four germicidin homologs have been isolated from Streptomyces coelicor: germicidin A, germicidin B, germicidin C, and surugapyrone A (germicidin D). All compounds inhibit spore germination. Germicidin A exhibits reversible inhibition as well as having activity resulting in hyphal elongation.
Biosynthesis
Biosynthesis of the germicidin A,B, and C is achieved through a type III polyketide synthase called germicidin synthase (Gcs). Surugapyrone A is expected to be synthesized similarly utilizing a Gcs homolog. Gcs exhibits high substrate flexibility accepting a variety of acyl groups carried and transferred through a thioester bond by either coenzyme A (CoA) or acyl carrier protein (ACP). Catalytic efficiency is tenfold higher when ACP is the acyl carrier. Crystal structures of Gcs indicate a characteristic type III structure with the exception of an unusual insertion of 40-residues at the dimer interface.
The biosynthetic pathway of germicidin has not been fully confirmed but according to experimental evidence is expected to utilize starter units arising from fatty acid synthesis and utilize the following proposed scheme: AcpP(ACP) is converted from its apo to holo form with CoA and AcpS (ACP synthase). FabD then converts holo-AcpP into malonyl-AcpP with malonyl-CoA. With either isobutyryl-CoA or 2-methylbutyryl-CoA FabH facilitates decarboxylative condensation with malonyl-AcpP to generate an acyl-AcpP intermediate. The acyl intermediate is then condensed and cyclized with either methylmalonyl-CoA or ethylmalonyl-CoA by Gcs to produce germicidin.
Types
letter | 3- position | 6- position |
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A | ethyl | sec-butyl |
B | ethyl | isopropyl |
C | ||
D | methyl | isopropyl |
F | 2-methylpropyl | propan |
G | 2-methylpropyl | butyl |
H | methyl | propyl |
I | methyl | 2-methylpropyl |
J | methyl | butyl |
References
- ^ Aoki, Y; Matsumoto, D; Kawaide, H; Natsume, M (September 2011). "Physiological role of germicidins in spore germination and hyphal elongation in Streptomyces coelicolor A3(2)". The Journal of Antibiotics. 64 (9): 607–11. doi:10.1038/ja.2011.59. PMID 21792209.
- ^ Petersen, F; Zähner, H; Metzger, JW; Freund, S; Hummel, RP (July 1993). "Germicidin, an autoregulative germination inhibitor of Streptomyces viridochromogenes NRRL B-1551". The Journal of Antibiotics. 46 (7): 1126–38. doi:10.7164/antibiotics.46.1126. PMID 8360109.
- ^ Chemler, JA; Buchholz, TJ; Geders, TW; Akey, DL; Rath, CM; Chlipala, GE; Smith, JL; Sherman, DH (May 2, 2012). "Biochemical and Structural Characterization of Germicidin Synthase: Analysis of a Type III Polyketide Synthase That Employs Acyl-ACP as a Starter Unit Donor". Journal of the American Chemical Society. 134 (17): 7359–66. doi:10.1021/ja2112228. PMC 3342439. PMID 22480290.