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对具有强抗氧化活性的KACC92338菌株进行全基因组测序,揭示了具有益生菌和抗菌潜力的基因及基因簇。

Whole genome sequencing of KACC92338 strain with strong antioxidant activity, reveals genes and gene clusters of probiotic and antimicrobial potential.

作者信息

Kandasamy Sujatha, Lee Kil-Ho, Yoo Jayeon, Yun Jeonghee, Kang Han Byul, Kim Ji Eun, Oh Mi-Hwa, Ham Jun-Sang

机构信息

Animal Products Research and Development Division, National Institute of Animal Science, Rural Development Administration, Wanju-gun, Republic of Korea.

出版信息

Front Microbiol. 2024 Sep 26;15:1458221. doi: 10.3389/fmicb.2024.1458221. eCollection 2024.

DOI:10.3389/fmicb.2024.1458221
PMID:39391606
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11464305/
Abstract

KACC92338 was originally isolated from Korean raw milk. The antioxidant activities and protective effect of this strain were evaluated extensively. The results showed that KACC92338 can tolerate hydrogen peroxide up to 2 mM and cell-free supernatant (CFS) had higher scavenging rates for DPPH, hydroxyl radical, reducing power, and iron chelating activities with 95.61 ± 1.59%, 34.10 ± 1.93%, 2.220 ± 0.82 and 81.06 ± 1.06%, respectively. Meanwhile, the CFS showed a protective effect on yeast cells against 10 mM hydrogen peroxide with a survival rate of 76.05 ± 5.65%. To explore the probiotic potential of KACC92338, whole genome assembly and gene clusters with probiotic properties were further analyzed. The genome size was 3,050,901 bp with a 47.96% GC ratio, and 63 contigs. The genome contains 3,048 genes composed of 2,981 coding sequences and 67 RNAs (including 57 tRNAs +9 rRNAs +1 tmRNA). Average Nucleotide Identity and genome-based taxonomy showed that the KACC92338 genome had close similarity with strains with 96% ANI. Functional annotation by EggNOG and KEGG revealed the presence of numerous genes putatively involved in carbohydrate- and amino acid-transport and metabolism, genetic information processing, and signaling and cellular processes. Additionally, several genes conferring probiotic characteristics such as tolerance to stress, heat, cold, acid, bile salts, oxidative stress, immunomodulation, and adhesion to intestinal epithelium were identified. Notably absent were acquired antibiotic resistance genes, virulence, and pathogenic factors, that prove KACC92338 is a safe strain. Besides, the defense mechanisms of KACC92338 include six prophage regions and three clustered regularly interspaced short palindromic repeat (CRISPR) arrays as acquired immune systems against mobile elements. Further, the BAGEL4 database determined antimicrobial bacteriocin clusters of class IIb: sakacin-P, Enterolysin_A, sactipeptides, and Enterocin X, which suggests the strain could exhibit a wide range of antimicrobial functions. Together, these findings show that the KACC92338 strain can be a potential probiotic candidate in producing functional fermented foods-, health care- and skin care products- with antioxidant properties. However, a few more mechanistic studies are necessary on the safety assurance and potential application of the strain as a probiotic agent.

摘要

KACC92338最初从韩国生牛奶中分离得到。对该菌株的抗氧化活性和保护作用进行了广泛评估。结果表明,KACC92338能够耐受高达2 mM的过氧化氢,其无细胞上清液(CFS)对DPPH、羟基自由基、还原力和铁螯合活性具有较高的清除率,分别为95.61±1.59%、34.10±1.93%、2.220±0.82和81.06±1.06%。同时,CFS对酵母细胞具有保护作用,可抵抗10 mM过氧化氢,存活率为76.05±5.65%。为了探索KACC92338的益生菌潜力,进一步分析了全基因组组装和具有益生菌特性的基因簇。基因组大小为3,050,901 bp,GC含量为47.96%,共有63个重叠群。该基因组包含3,048个基因,由2,981个编码序列和67个RNA组成(包括57个tRNA + 9个rRNA + 1个tmRNA)。平均核苷酸同一性和基于基因组的分类学表明,KACC92338基因组与ANI为96%的菌株具有密切相似性。通过EggNOG和KEGG进行的功能注释揭示了许多可能参与碳水化合物和氨基酸运输与代谢、遗传信息处理以及信号传导和细胞过程的基因。此外,还鉴定了几个赋予益生菌特性的基因,如对压力、热、冷、酸、胆汁盐、氧化应激的耐受性、免疫调节以及对肠上皮的粘附性。值得注意的是,该菌株不存在获得性抗生素耐药基因、毒力和致病因子,这证明KACC92338是一种安全的菌株。此外,KACC92338的防御机制包括六个前噬菌体区域和三个成簇规律间隔短回文重复序列(CRISPR)阵列,作为针对移动元件的获得性免疫系统。此外,BAGEL4数据库确定了IIb类抗微生物细菌素簇:片球菌素-P、肠球菌素_A、sactipeptides和肠球菌素X,这表明该菌株可能具有广泛的抗微生物功能。总之这些研究结果表明,KACC92338菌株可能是生产具有抗氧化特性的功能性发酵食品、保健品和护肤品的潜在益生菌候选菌株。然而,还需要对该菌株作为益生菌剂的安全性保证和潜在应用进行更多的机制研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/3a14628fda5b/fmicb-15-1458221-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/8acc80fd8306/fmicb-15-1458221-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/b01c36b957af/fmicb-15-1458221-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/0747558a90c9/fmicb-15-1458221-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/1b74eba02601/fmicb-15-1458221-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/3a14628fda5b/fmicb-15-1458221-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/8acc80fd8306/fmicb-15-1458221-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/b01c36b957af/fmicb-15-1458221-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/0747558a90c9/fmicb-15-1458221-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/1b74eba02601/fmicb-15-1458221-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/11464305/3a14628fda5b/fmicb-15-1458221-g005.jpg

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