Novel bifidobacterium longum strain or cosmetic composition comprising same
A technology of bifidobacterium longum and strains, applied in the direction of bifidobacteria, cosmetics, cosmetic preparations, etc., can solve the problems of pigmentation and melanin deposition in multiple places, and achieve the effect of enhancing skin beauty and improving skin health
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Embodiment 1
[0112]
[0113] Bifidobacterium longum (hereinafter referred to as F5) was isolated from donated feces of newborns (babies born in 2018, Daejeon, Korea). To this end, neonatal feces were diluted with 0.9% (w / v) saline by a 10-fold serial dilution method, and the resulting solution was spread on a bifidobacterium selective (BS, MBcell Seoul, Korea) solid medium and incubated at 37°C. Incubate the bacteria for 48 hours. The bacterial colonies produced in the BS medium were observed with a microscope. By observation, bacteria and bacillus-type bacteria that did not exhibit a catalase reaction were selected and named ATG-F5 strain (hereinafter abbreviated as F5). For the experiments, F5 strains were first cultured in BL or MRS-cys agar solid medium, and then purely isolated colonies were inoculated in broth liquid medium. Microorganisms were incubated overnight (ie for 16 to 20 hours) at 37°C.
Embodiment 2
[0114]
Embodiment 2-1
[0115] Example 2-1. F5 strain 16S rRNA sequencing
[0116] Upon request, Solgent Co., Ltd. (located in Dajeon, Korea) performed 16S rRNA sequence analysis on the F5 strain. Primers used for sequencing analysis were:
[0117] 27F(5'-AGA GTT TGA TCC TGGCTC AG-3'), 518F(5'-CCA GCA GCC GCG GTA ATAC-3'), 907R(5'-CCGTCA ATT CMT TTR AGT TT-3'), 1492R( 5′-GGT TAC CTT GTT ACG ACTT-3′), and the nucleotide sequence was read 4 times in total. Contigs derived from nucleotide sequence alignments of each read were analyzed using the National Center for Biotechnology Information (NCBI) BLAST online tool (https: / / blast.ncbi.nlm.nih.gov / Blast.cgi) Nucleotide sequence.
[0118] The nucleotide sequence of SEQ ID NO:1 obtained by 16S rRNA sequencing (see figure 1 ) were compared with NCBI's BLAST database. As a result, the B. longum strain IRT showed a 99.9% match with the 16S rRNA sequence, thereby indicating that the tested sequence belongs to B. longum when classified by molecular taxonomy...
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