Evidence map›Paper›PMID 41085814›Full record

ArticleMolecular biology reports2025

Genome mining identifies Micrococcus yunnanensis strain AZMABM 17 as a potential source of Antioxidant, Anti-Inflammatory, Antidiabetic, and Antiproliferative compounds.

Herman Irawan, Apon Zaenal Mustopa, Ramadhika Pra Suryadinata, Andi Baso Manguntungi, Joko Pebrianto Trinugroho, Feraliana, Wike Zahra Mustafawi, Mochamad Untung Kurnia Agung, Agus Budiawan Naro Putra, Kartika Dyah Palupi

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Herman IrawanResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Jl. Raya Jakarta Bogor KM 46, Bogor, West Java, 16911, Indonesia.
Apon Zaenal MustopaResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Jl. Raya Jakarta Bogor KM 46, Bogor, West Java, 16911, Indonesia. azae001@brin.go.id.
Ramadhika Pra SuryadinataDepartment of Marine Science, Faculty of Fisheries and Marine Science, Universitas Padjadjaran, Sumedang, West Java, 45363, Indonesia.
Andi Baso ManguntungiDepartment of Biotechnology, Faculty of Mathematics and Natural Sciences, Universitas Sulawesi Barat, Jl. Prof Baharuddin Lopa, Majene, West Sulawesi, 91412, Indonesia.
Joko Pebrianto TrinugrohoResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Jl. Raya Jakarta Bogor KM 46, Bogor, West Java, 16911, Indonesia.
FeralianaResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Jl. Raya Jakarta Bogor KM 46, Bogor, West Java, 16911, Indonesia.
Wike Zahra MustafawiResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Jl. Raya Jakarta Bogor KM 46, Bogor, West Java, 16911, Indonesia.
Mochamad Untung Kurnia AgungDepartment of Marine Science, Faculty of Fisheries and Marine Science, Universitas Padjadjaran, Sumedang, West Java, 45363, Indonesia.
Agus Budiawan Naro PutraResearch Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Jl. Raya Jakarta Bogor KM 46, Bogor, West Java, 16911, Indonesia.
Kartika Dyah PalupiResearch Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Jl. Raya Jakarta Bogor KM 46, Bogor, West Java, 16911, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe discovery and characterization of novel microbial strains are critical for advancing our understanding of microbial diversity and their potential applications in biotechnology and medicine.

methodsIn this study, we identified and characterized Micrococcus yunnanensis strain AZMABM 17 using 16 S rRNA sequencing and Average Nucleotide Identity (ANI) analysis. Whole-genome sequencing was performed to determine the genomic structure and functional potential of the strain. Functional annotation and predictive analysis of secondary metabolite biosynthesis gene clusters (BGCs) were also conducted. The bioactivity of the isolate was evaluated through antidiabetic, antioxidant, and anti-inflammatory assays by measuring inhibition using a spectrophotometer. Antiproliferative activity was assessed using MTT assays against the MCF-7 breast cancer cell line.

resultsThe 16 S rRNA sequencing revealed a 98.28% identity with Micrococcus sp. 3455 and Micrococcus sp. GS57, while ANI analysis showed a 98.30% similarity with Micrococcus yunnanensis DSM 21,948, confirming AZMABM 17 as a novel strain. Whole-genome sequencing revealed a circular chromosome of 2,435,094 base pairs with a GC content of 73%, encoding 2,183 protein-coding genes, including 949 assigned to Gene Ontology (GO) and 1,367 to KEGG Orthology (KO). Functional annotation identified genes involved in amino acid transport, carbohydrate metabolism, and secondary metabolite biosynthesis, including terpenoids and carotenoids. The strain exhibited significant antioxidant, antidiabetic, anti-inflammatory, and antiproliferative activities, with higher metabolite concentrations correlating with increased bioactivities. Predictive analysis identified six putative secondary metabolite biosynthesis gene clusters (BGCs), including terpene and NI-siderophore clusters, suggesting the potential to produce novel bioactive compounds.

conclusionsThese findings underscore the biotechnological potential of Micrococcus yunnanensis strain AZMABM 17, particularly in pharmaceutical and environmental applications.

Indexed as

AntioxidantsMicrococcusAnti-Inflammatory AgentsCell ProliferationGenome, BacterialHumansHypoglycemic AgentsMCF-7 CellsMultigene FamilyPhylogenyRNA, Ribosomal, 16SWhole Genome SequencingAnti-Inflammatory AgentsAntioxidantsHypoglycemic AgentsRNA, Ribosomal, 16SAnti-inflammatoryAntioxidantBioactive compounds.Biotechnological potentialMicrococcus yunnanensisSecondary metabolitesWhole-genome sequencing

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.