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Aminocyclitol

From Wikipedia, the free encyclopedia

The aminocyclitols are compounds related to cyclitols. They possess features of relative and absolute configuration that are characteristic of their class and have been extensively studied; but these features are not clearly displayed by general methods of stereochemical nomenclature, so that special methods of specifying their configuration are justified and have long been used. In other than stereochemical respects, their nomenclature should follow the general rules of organic chemistry.[1]

Aminocyclitol natural products

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The aminocyclitol family of natural products is a class of sugar-derived microbial secondary metabolites that demonstrate significant biological activities. Aminocyclitols are found as a component of aminoglycoside antibiotics which is also called as pseudosugars or pseudosaccharides. Aminocyclitols have chemical structures of a carbon ring with amine functional group(s). The class of aminocyclitol containing natural products can be divided by ring sizes or types of precursors.

Five-membered ring aminocyclitols

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pactamycin

Six-membered ring aminocyclitols

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  • 2-deoxy-scyllo-inosose derived aminoglycosides

This class includes kanamycin, neomycin, gentamicin, apramycin, hygromycin.

  • myo-inositol 1-phosphate derived aminoglycosides

This class includes streptomycin, spectinomycin.

  • sedoheptulose 7-phosphate derived C7N aminocyclitol natural products

This class includes acarbose, validamycin, validoxylamine A,[2] salbostatin, cetoniacytone A,[3] pyralomicin 1a,[4] kirkamide[5]

Biosynthesis of C7N aminocyclitols

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Sedoheptulose 7-phosphate, a pentose phosphate pathway intermediate, is a common precursor of C7N aminocyclitol moiety of natural products, such as acarbose,[6] validamycin A,[7] salbostatin,[8] cetoniacytone A,[9][10] and pyralomicin 1a.[11] 2-epi-5-epi-valiolone synthase (EEVS),[6][12][13] one of the sugar phosphate cyclase family enzyme[9] and which is a homolog of 3-dehydroquinate synthase in shikimate pathway, catalyzes the formation of a common intermediate, 2-epi-5-epi-valiolone from sedoheptulose 7-phosphate. After multiple enzyme reaction steps, which include phosphorylation,[14][15] epimerization,[16] dehydration, and keto-reduction reactions, valienol, an important core structure is formed which leads to the formation of C7N aminocyclitol containing natural products. In validamycin biosynthesis, the C-N linkage which connect the C7 cyclitol moiety to the other was found to be formed by unprecedented actions of nucleotidyltransferase[17] and glycosyltransferase-like enzymes[18][19][20] (which is termed pseudoglycosyltransferase).

References

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  1. ^ "cyclitols". www.chem.qmul.ac.uk. Retrieved 2016-01-08.
  2. ^ Asamizu, Shumpei; Abugreen, Mostafa; Mahmud, Taifo (2013). "Comparative metabolomic analysis of an alternative biosynthetic pathway to pseudosugars in Actinosynnema mirum DSM 43827". ChemBioChem. 14 (13): 1548–1551. doi:10.1002/cbic.201300384. PMC 3835175. PMID 23939727.
  3. ^ Schlörke, Oliver; Krastel, Philipp; Müller, Ilka; Usón, Isabel; Dettner, Konrad; Zeeck, Axel (2002). "Structure and biosynthesis of cetoniacytone A, a cytotoxic aminocarba sugar produced by an endosymbiontic Actinomyces". The Journal of Antibiotics. 55 (7): 635–642. doi:10.7164/antibiotics.55.635. PMID 12243453.
  4. ^ Naganawa, Hiroshi; Hashizume, Hideki; Kubota, Yumiko; Sawa, Ryuichi; Takahashi, Yoshikazu; Arakawa, Kenji; Bowers, Simeon G.; Mahmud, Taifo (2002). "Biosynthesis of the cyclitol moiety of pyralomicin 1a in Nonomuraea spiralis MI178-34F18". The Journal of Antibiotics. 55 (6): 578–584. doi:10.7164/antibiotics.55.578. PMID 12195964.
  5. ^ Sieber, Simon; Carlier, Aurélien; Neuburger, Markus; Grabenweger, Giselher; Eberl, Leo; Gademann, Karl (2015). "Isolation and Total Synthesis of Kirkamide, an Aminocyclitol from an Obligate Leaf Nodule Symbiont" (PDF). Angewandte Chemie International Edition in English. 54 (27): 7968–7970. doi:10.1002/anie.201502696. PMID 26033226.
  6. ^ a b Stratmann, Ansgar; Mahmud, Taifo; Lee, Sungsook; Distler, Juergen; Floss, Heinz G.; Piepersberg, Wolfgang (1999). "The AcbC Protein from Actinoplanes Species Is a C7-cyclitol Synthase Related to 3-Dehydroquinate Synthases and Is Involved in the Biosynthesis of the α-Glucosidase Inhibitor Acarbose". Journal of Biological Chemistry. 274 (16): 10889–10896. doi:10.1074/jbc.274.16.10889. PMID 10196166.
  7. ^ Yu, Yi; Bai, Linquan; Minagawa, Kazuyuki; Jian, Xiaohong; Li, Lei; Li, Jialiang; Chen, Shuangya; Cao, Erhu; Mahmud, Taifo (2005). "Gene cluster responsible for validamycin biosynthesis in Streptomyces hygroscopicus subsp. jinggangensis 5008". Applied and Environmental Microbiology. 71 (9): 5066–5076. doi:10.1128/AEM.71.9.5066-5076.2005. PMC 1214664. PMID 16151088.
  8. ^ Choi, Woo Sik; Wu, Xiumei; Choeng, Yong-Hoon; Mahmud, Taifo; Jeong, Byeong Chul; Lee, Sang Hee; Chang, Yong Keun; Kim, Chang-Joon; Hong, Soon-Kwang (2008). "Genetic organization of the putative salbostatin biosynthetic gene cluster including the 2-epi-5-epi-valiolone synthase gene in Streptomyces albus ATCC 21838". Applied Microbiology and Biotechnology. 80 (4): 637–645. doi:10.1007/s00253-008-1591-2. PMID 18648803. S2CID 12324872.
  9. ^ a b Wu, Xiumei; Flatt, Patricia M.; Schlörke, Oliver; Zeeck, Axel; Dairi, Tohru; Mahmud, Taifo (2007). "A Comparative Analysis of the Sugar Phosphate Cyclase Superfamily Involved in Primary and Secondary Metabolism". ChemBioChem. 8 (2): 239–248. doi:10.1002/cbic.200600446. PMC 3127856. PMID 17195255.
  10. ^ Wu, Xiumei; Flatt, Patricia M.; Xu, Hui; Mahmud, Taifo (2009). "Biosynthetic Gene Cluster of Cetoniacytone A, an Unusual Aminocyclitol from the Endosymbiotic Bacterium Actinomyces sp. Lu 9419". ChemBioChem. 10 (2): 304–314. doi:10.1002/cbic.200800527. PMC 3136446. PMID 19101977.
  11. ^ Flatt, Patricia M.; Wu, Xiumei; Perry, Steven; Mahmud, Taifo (2013). "Genetic Insights into Pyralomicin Biosynthesis in Nonomuraea spiralis IMC A-0156". Journal of Natural Products. 76 (5): 939–946. doi:10.1021/np400159a. PMC 3684624. PMID 23607523.
  12. ^ Asamizu, Shumpei; Xie, Pengfei; Brumsted, Corey J.; Flatt, Patricia M.; Mahmud, Taifo (2012). "Evolutionary divergence of sedoheptulose 7-phosphate cyclases leads to several distinct cyclic products". Journal of the American Chemical Society. 134 (29): 12219–12229. doi:10.1021/ja3041866. PMC 3405187. PMID 22741921.
  13. ^ Kean, Kelsey M.; Codding, Sara J.; Asamizu, Shumpei; Mahmud, Taifo; Karplus, P. Andrew (2014). "Structure of a sedoheptulose 7-phosphate cyclase: ValA from Streptomyces hygroscopicus". Biochemistry. 53 (26): 4250–4260. doi:10.1021/bi5003508. PMC 4095911. PMID 24832673.
  14. ^ Zhang, Chang-Sheng; Stratmann, Ansgar; Block, Oliver; Brückner, Ralph; Podeschwa, Michael; Altenbach, Hans-Josef; Wehmeier, Udo F.; Piepersberg, Wolfgang (2002). "Biosynthesis of the C7-cyclitol Moiety of Acarbose inActinoplanes Species SE50/110 7-O-PHOSPHORYLATION OF THE INITIAL CYCLITOL PRECURSOR LEADS TO PROPOSAL OF A NEW BIOSYNTHETIC PATHWAY". Journal of Biological Chemistry. 277 (25): 22853–22862. doi:10.1074/jbc.m202375200. PMID 11937512.
  15. ^ Minagawa, Kazuyuki; Zhang, Yirong; Ito, Takuya; Bai, Linquan; Deng, Zixin; Mahmud, Taifo (2007). "ValC, a New Type of C7-Cyclitol Kinase Involved in the Biosynthesis of the Antifungal Agent Validamycin A". ChemBioChem. 8 (6): 632–641. doi:10.1002/cbic.200600528. PMC 3136165. PMID 17335096.
  16. ^ Xu, Hui; Zhang, Yirong; Yang, Jongtae; Mahmud, Taifo; Bai, Linquan; Deng, Zixin (2009). "Alternative epimerization in C(7)N-aminocyclitol biosynthesis is catalyzed by ValD, a large protein of the vicinal oxygen chelate superfamily". Chemistry & Biology. 16 (5): 567–576. doi:10.1016/j.chembiol.2009.04.006. PMC 2737586. PMID 19477421.
  17. ^ Yang, Jongtae; Xu, Hui; Zhang, Yirong; Bai, Linquan; Deng, Zixin; Mahmud, Taifo (2011). "Nucleotidylation of unsaturated carbasugar in validamycin biosynthesis". Organic & Biomolecular Chemistry. 9 (2): 438–449. doi:10.1039/c0ob00475h. PMC 3124559. PMID 20981366.
  18. ^ Asamizu, Shumpei; Yang, Jongtae; Almabruk, Khaled H.; Mahmud, Taifo (2011). "Pseudoglycosyltransferase catalyzes nonglycosidic C-N coupling in validamycin a biosynthesis". Journal of the American Chemical Society. 133 (31): 12124–12135. doi:10.1021/ja203574u. PMC 3162038. PMID 21766819.
  19. ^ Cavalier, Michael C.; Yim, Young-Sun; Asamizu, Shumpei; Neau, David; Almabruk, Khaled H.; Mahmud, Taifo; Lee, Yong-Hwan (2012). "Mechanistic insights into validoxylamine A 7'-phosphate synthesis by VldE using the structure of the entire product complex". PLOS ONE. 7 (9): e44934. doi:10.1371/journal.pone.0044934. PMC 3441724. PMID 23028689.
  20. ^ Abuelizz, Hatem A.; Mahmud, Taifo (2015). "Distinct Substrate Specificity and Catalytic Activity of the Pseudoglycosyltransferase VldE". Chemistry & Biology. 22 (6): 724–733. doi:10.1016/j.chembiol.2015.04.021. PMC 4475420. PMID 26051218.
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