Aldo Betancourt Sanchez, Alexander Huynh, Laurence Blanchard, Arjan De Groot, Christophe Klopp, Karine Loubière, Caroline Andriantsiferana, Barbora Lajoie
{"title":"Zeaxanthin-Producing Winogradskyella schleiferi Strains","authors":"Aldo Betancourt Sanchez, Alexander Huynh, Laurence Blanchard, Arjan De Groot, Christophe Klopp, Karine Loubière, Caroline Andriantsiferana, Barbora Lajoie","doi":"10.1002/jobm.70187","DOIUrl":null,"url":null,"abstract":"<p>Two pigmented bacteria strains were isolated from the Mediterranean Sea. Phylogenetic analysis revealed that both strains are affiliated with <i>Winograsdskyella schleiferi</i> Z215. However, in contrast to this reference strain, they can assimilate additional carbon sources such as <span>d</span>-mannose, <span>l</span>-arabinose, <span>d</span>-mannitol, and citrate. Zeaxanthin was identified as the major carotenoid produced by both strains, predominantly in the <i>all-trans</i> configuration. Carotenoid biosynthesis kinetics revealed that pigment production commenced at the early stages of growth, with maximal yields reached between 48 and 56 h (between 1 and 1.3 mg L<sup>−1</sup>). Specific production yields were 0.7 and 0.9 mg g<sup>−1</sup> for the two strains, respectively. Total carotenoid production was influenced by incubation temperature in both strains. Overall, these findings expand the scientific knowledge on carotenoid-producing marine bacteria and highlight the potential of these newly isolated strains as promising candidates for zeaxanthin biotechnological production for a wide range of novel applications ranging from feed additives to treatments for macular degeneration and melanoma.</p>","PeriodicalId":15101,"journal":{"name":"Journal of Basic Microbiology","volume":"66 7","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2026-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jobm.70187","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Basic Microbiology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jobm.70187","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Two pigmented bacteria strains were isolated from the Mediterranean Sea. Phylogenetic analysis revealed that both strains are affiliated with Winograsdskyella schleiferi Z215. However, in contrast to this reference strain, they can assimilate additional carbon sources such as d-mannose, l-arabinose, d-mannitol, and citrate. Zeaxanthin was identified as the major carotenoid produced by both strains, predominantly in the all-trans configuration. Carotenoid biosynthesis kinetics revealed that pigment production commenced at the early stages of growth, with maximal yields reached between 48 and 56 h (between 1 and 1.3 mg L−1). Specific production yields were 0.7 and 0.9 mg g−1 for the two strains, respectively. Total carotenoid production was influenced by incubation temperature in both strains. Overall, these findings expand the scientific knowledge on carotenoid-producing marine bacteria and highlight the potential of these newly isolated strains as promising candidates for zeaxanthin biotechnological production for a wide range of novel applications ranging from feed additives to treatments for macular degeneration and melanoma.
期刊介绍:
The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions.
Papers published deal with:
microbial interactions (pathogenic, mutualistic, environmental),
ecology,
physiology,
genetics and cell biology/development,
new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications)
novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).