Isolation and Cultivation of Carotenoid-Producing Strains from Tidal Flat Sediment and Proposal of Croceibacterium aestuarii sp. nov., a Novel Carotenoid-Producing Species in the Family Erythrobacteraceae

Abstract

Carotenoids are extensively used in drugs, cosmetics, nutrients, and foods, owing to their antioxidant and anti-inflammatory characteristics. Diverse marine heterotrophic prokaryotes can accumulate carotenoids and become promising alternatives for the advancement of carotenoids production. In this research, 55 strains were isolated and cultivated from tidal flat sediment in Zhoushan and classified into the phyla Pseudomonadota (n = 24), Bacillota (n = 18), Bacteroidota (n = 9), and Actinomycetota (n = 4). Nine of them accumulated carotenoids, and most of them belonged to the families Flavobacteriaceae (n = 4) and Erythrobacteraceae (n = 4). Among those carotenoid-producing strains, one strain, designated as D39T, was proposed as one novel species belonging to the genus Croceibacterium through polyphasic taxonomy approaches. Genomic annotations and carotenoid compound determinations revealed that strain D39T encoded crtEBIYZG genes and mainly accumulated zeaxanthin as major carotenoids. Furthermore, carotenoid biosynthesis pathway in the majority of Croceibacterium strains were identical with that in the strain D39T, implying that Croceibacterium members can be sources of producing zeaxanthin. This study enhances knowledge of microbial biodiversity in tidal flats, proposes a novel carotenoid-producing Croceibacterium species, and elucidates carotenoid biosynthesis pathway in the genus Croceibacterium, which contribute to enriching marine carotenoid-producing strains and promoting a comprehensive insight into genomic contents of them.

Aurantiacibacter hainanensis sp. nov. and Qipengyuania zhejiangensis sp. nov., two novel Erythrobacteraceae species isolated from tidal flat sediments

“…The presence of carotenoids was detected by using spectrophotometry, as described by Xu et al . [35]. The cells in MB medium were centrifuged, the supernatant was removed, washed with 2.0 % (w/v) NaCl solution, and centrifuged again.…”