CRISPR/Cas9-Mediated Metabolic Engineering of Endophytic Pseudomonas Loganensis Sp. Nov. for the Production of Nutritionally Valuable Carotenoids

dc.contributor.author Arslansoy, Nuriye
dc.contributor.author Karaman, Melisa Zulal
dc.contributor.author Fidan, Ozkan
dc.date.accessioned 2026-01-20T15:32:24Z
dc.date.available 2026-01-20T15:32:24Z
dc.date.issued 2026
dc.description.abstract Carotenoids with significant nutritional and antioxidant properties have been widely utilized in the food, feed, pharmaceutical, and cosmetic industries. They improve the nutritional value of foodstuffs and have been used as natural food colorants. However, their current supply chain is mainly dependent on extraction from plants and chemical synthesis, both of which have bottlenecks, including environmental concerns, toxicity, and allergenicity. To address global demand for sustainable and environmentally friendly production of nutrients, we engineered the endophytic Pseudomonas loganensis sp. nov. as a niche microbial chassis for nutritionally valuable carotenoid production. Using CRISPR-Cas9, we knocked out key carotenogenic genes to construct strains capable of producing zeaxanthin, lycopene, and beta-carotene. Additionally, an overexpression plasmid was introduced to produce astaxanthin. HPLC analysis confirmed the successful production of four target carotenoids. The culture conditions and media compositions were optimized using response surface methodology, resulting in a similar to 5-fold increase in the titers of zeaxanthin (13.4 mg/L), lycopene (9.67 mg/L), and beta-carotene (23.53 mg/L), and a similar to 12-fold increase in astaxanthin titer (1 mg/L) compared to LB medium without optimization. Our results indicate the potential of endophytic bacteria as a microbial chassis for carotenoid bioproduction, underscoring the potential of synthetic biology to contribute to global efforts toward nutritional security and sustainable food systems. en_US
dc.description.sponsorship Trkiye Bilimsel ve Teknolojik Arastirma Kurumu [221Z280] en_US
dc.description.sponsorship We sincerely thank Prof. Zulal Kesmen and her PhD candidate, Melike Canpolat, for their generosity in sharing their electroporation equipment and for warmly welcoming us into their lab. We also extend our heartfelt gratitude to Prof. Brian F. Pfleger for generously providing the CRISPR-Cas9 plasmids used in this study. Additionally, we gratefully acknowledge the financial support of TUBITAK under 3501 Career Development Program (Project No.: 221Z280), which made this research possible. en_US
dc.identifier.doi 10.1021/acsomega.5c05877
dc.identifier.issn 2470-1343
dc.identifier.uri https://doi.org/10.1021/acsomega.5c05877
dc.identifier.uri https://hdl.handle.net/20.500.12573/5753
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.relation.ispartof ACS Omega en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title CRISPR/Cas9-Mediated Metabolic Engineering of Endophytic Pseudomonas Loganensis Sp. Nov. for the Production of Nutritionally Valuable Carotenoids en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.wosid Fidan, Ozkan/Aag-4659-2019
gdc.description.department Abdullah Gül Üniversitesi en_US
gdc.description.departmenttemp [Arslansoy, Nuriye; Karaman, Melisa Zulal] Abdullah Gul Univ, Grad Sch Sci & Engn, Dept Bioengn, TR-38080 Kayseri, Turkiye; [Fidan, Ozkan] Abdullah Gul Univ, Fac Nat & Life Sci, Dept Bioengn, TR-38080 Kayseri, Turkiye en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.wos WOS:001653559900001
gdc.virtual.author Fidan, Özkan
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