Lipstatin

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Lipstatin
Lipstatin.svg
Names
Systematic IUPAC name
(2S,4Z,7Z)-1-[(2S,3S)-3-Hexyl-4-oxooxetan-2-yl]trideca-4,7-dien-2-yl (2S)-2-formamido-4-methylpentanoate
Other names
(2S,4Z,7Z)-1-[(2S,3S)-3-Hexyl-4-oxo-2-oxetanyl]-4,7-tridecadien-2-yl N-formyl-L-leucinate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.126.007 OOjs UI icon edit-ltr-progressive.svg
MeSH Lipstatin
PubChem CID
UNII
  • InChI=1S/C29H49NO5/c1-5-7-9-11-12-13-14-15-16-18-24(34-29(33)26(30-22-31)20-23(3)4)21-27-25(28(32)35-27)19-17-10-8-6-2/h12-13,15-16,22-27H,5-11,14,17-21H2,1-4H3,(H,30,31)/b13-12-,16-15-/t24-,25-,26-,27-/m0/s1 Yes check.svgY
    Key: OQMAKWGYQLJJIA-CUOOPAIESA-N Yes check.svgY
  • InChI=1/C29H49NO5/c1-5-7-9-11-12-13-14-15-16-18-24(34-29(33)26(30-22-31)20-23(3)4)21-27-25(28(32)35-27)19-17-10-8-6-2/h12-13,15-16,22-27H,5-11,14,17-21H2,1-4H3,(H,30,31)/b13-12-,16-15-/t24-,25-,26-,27-/m0/s1
    Key: OQMAKWGYQLJJIA-CUOOPAIEBU
  • O=C(O[C@H](C[C@@H]1OC(=O)[C@H]1CCCCCC)C\C=C/C\C=C/CCCCC)[C@@H](NC=O)CC(C)C
Properties
C29H49NO5
Molar mass 491.713 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Lipstatin is a potent, irreversible inhibitor of pancreatic lipase. It is a natural product that was first isolated from the actinobacterium Streptomyces toxytricini . [1]

Contents

The popular antiobesity drug orlistat (trade names Xenical and alli) is a saturated derivative of lipstatin.

Biosynthesis

Lipstatin biosynthesis pathway in Streptomyces toxytricini. Biosynthesis of lipstatin.jpg
Lipstatin biosynthesis pathway in Streptomyces toxytricini.

Lipstatin is composed of a 2-hexyl-3,5-dihydroxy-7,10-hexadecadienoic-β-lactone 22 carbon backbone from fatty acid synthesis pathway and an N-formyl-L-leucine group ester linked to the 5-hydroxyl group of the back bone. The composts of the lipstatin are ultimately from linoleic acid, octanoic acid, and L-leucine. [2]

The 22 carbon β-lactone moiety is derived from Claisen condensation between 3-hydroxytetradeca-5,8-dienyl-CoA derived from linoleic acid and hexyl-malonyl-ACP derived from octanoic acid. [2] [3] [4] Linoleic acid is first attached to CoA through some acyl-CoA synthetase homologue synthesized by lipstatin biosynthetic operons (Lst) and goes through two β-oxidation to hydroxytetradeca-5,8-dienyl-CoA. 3’ hydroxyl group from solution H2O is added by enoyl reductase homologue followed by enoyl hydratase homologue. [5] Octanoic acid is also attached to CoA through similar acyl-CoA synthetase homologue (LstC) to form octanoyl-CoA. Octanoyl-CoA is 2’ carboxylated and loaded to acyl carrier protein (ACP) borrowed from primary metabolism to form hexyl-malonyl-ACP. [4]

The β-lactone ring is formed by reduction of 3-keto group by 3-hydroxysteroid dehydrogenase homologue followed by a spontaneously nucleophilic attack of the 3-hydroxyl group on the carbonyl of the ACP-tether acyl intermediate. This step follows the esterification of the N-formyl-L-leucine group. [2]

The N-formyl-L-leucine group is derived from L-leucine. L-leucine was activated by LstE forming thioester and its α-amine group is formylated by LstF. Finally, 5-hydroxyl of 22 carbon β-lactone backbone nucleophilic attacks on the acyl carbon of the formyl-leucine and forms the lipstatin. [2]

See also

References

  1. ↑ Weibel E, Hadvary P, Hochuli E, Kupfer E, Lengsfeld H (1987). "Lipstatin, an inhibitor of pancreatic lipase, produced by Streptomyces toxytricini. I. Producing organism, fermentation, isolation and biological activity". J Antibiot (Tokyo). 40 (8): 1081–5. doi: 10.7164/antibiotics.40.1081 . PMID   3680018.
  2. 1 2 3 4 Bai, Tingli; Zhang, Daozhong; Lin, Shuangjun; Long, Qingshan; Wang, Yemin; Ou, Hongyu; Kang, Qianjin; Deng, Zixin; Liu, Wen (2014-12-15). "Operon for Biosynthesis of Lipstatin, the Beta-Lactone Inhibitor of Human Pancreatic Lipase". Applied and Environmental Microbiology. 80 (24): 7473–7483. Bibcode:2014ApEnM..80.7473B. doi:10.1128/AEM.01765-14. ISSN   0099-2240. PMC   4249243 . PMID   25239907.
  3. ↑ Goese, Markus; Eisenreich, Wolfgang; Kupfer, Ernst; Stohler, Peter; Weber, Wolfgang; Leuenberger, Hans G.; Bacher, Adelbert (2001-06-01). "Biosynthesis of Lipstatin. Incorporation of Multiply Deuterium-Labeled (5Z,8Z)-Tetradeca-5,8-dienoic Acid and Octanoic Acid". The Journal of Organic Chemistry. 66 (13): 4673–4678. doi:10.1021/jo010230b. ISSN   0022-3263. PMID   11421791.
  4. 1 2 Demirev, Atanas V.; Khanal, Anamika; Sedai, Bhishma R.; Lim, Si Kyu; Na, Min Kyun; Nam, Doo Hyun (2010-05-02). "The role of acyl-coenzyme A carboxylase complex in lipstatin biosynthesis of Streptomyces toxytricini". Applied Microbiology and Biotechnology. 87 (3): 1129–1139. doi:10.1007/s00253-010-2587-2. ISSN   0175-7598. PMC   2886142 . PMID   20437235.
  5. ↑ Goese, Markus; Eisenreich, Wolfgang; Kupfer, Ernst; Weber, Wolfgang; Bacher, Adelbert (2000-07-14). "Biosynthetic Origin of Hydrogen Atoms in the Lipase Inhibitor Lipstatin". Journal of Biological Chemistry. 275 (28): 21192–21196. doi: 10.1074/jbc.M003094200 . ISSN   0021-9258. PMID   10801870.
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