4.7 Article

Chlorosphaerolactylates A-D: Natural Lactylates of Chlorinated Fatty Acids Isolated from the Cyanobacterium Sphaerospermopsis sp. LEGE 00249

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 83, Issue 6, Pages 1885-1890

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.0c00072

Keywords

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Funding

  1. European Commission under the H2020 program, NoMorFilm Project [634588]
  2. FCT strategic funds [UIDB/04423/2020, UIDP/04423/2020]
  3. Fundacao para a Ciencia e a Tecnologia (FCT) fellowship [SFRH/BD/136367/2018]
  4. Programa de Ayudas a Grupos de Investigacion del Principado de Asturias [IDI/2018/000120]
  5. Programa Severo Ochoa de Ayudas Predoctorales para la Investigacion y Docencia from Principado de Asturias [BP16023]
  6. Planes Nacionales de I+D+i 2008-2011/2013-2016
  7. Instituto de Salud Carlos III
  8. Subdireccion General de Redes y Centros de Investigacion Cooperativa
  9. Ministerio de Economia y Competitividad
  10. Spanish Network for Research in Infectious Diseases - European Development Regional Fund A Way to Achieve Europe [REIPI RD12/0015/0013, REIPI RD16/0016/0010]
  11. operative program Intelligent Growth 2014-2020
  12. EMBRC-ERIC
  13. European Regional Development Fund (ERDF) through COMPETE2020-Operational Programme for Competitiveness and Internationalisation (POCI) [CIIMAR-PINFRA/22121/2016-ALG-01-0145-FEDER-022121]
  14. FCT/MCTES
  15. Fundação para a Ciência e a Tecnologia [SFRH/BD/136367/2018] Funding Source: FCT
  16. H2020 Societal Challenges Programme [634588] Funding Source: H2020 Societal Challenges Programme

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Four natural lactylates of chlorinated fatty acids, chlorosphaerolactylates A-D (1-4), were isolated from the methanolic extract of the cyanobacterium Sphaerospermopsis sp. LEGE 00249 through a combination of bioassay-guided and MS-guided approaches. Compounds 1-4 are esters of (mono-, di-, or tri)chlorinated lauric acid and lactic acid, whose structures were assigned on the basis of spectrometric and spectroscopic methods inclusive of 1D and 2D NMR experiments. High-resolution mass-spectrometry data sets also demonstrated the existence of other minor components that were identified as chlorosphaero(bis)lactylate analogues. The chlorosphaerolactylates were tested for potential antibacterial, antifungal, and antibiofilm properties using bacterial and fungal clinical isolates. Compounds 1-4 showed a weak inhibitory effect on the growth of Staphylococcus aureus S54F9 and Candida parapsilosis SMI416, as well as on the biofilm formation of coagulase-negative Staphylococcus hominis FI31.

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