Evidence map›Paper›PMID 40713485›Full record

ArticleBMC microbiology2025

Identification and whole genome sequencing analysis of Bacillus subtilis K35-1, a highly efficient cellulose in forage degrading bacterium.

Dan Wu, Jing Feng, Dongxu Wen, Hongzhuang Wang, Sijia Lu, Kun Li, Rizwana Sultan, Bin Li

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

8 authors.

Dan WuState Key Laboratory of Hulless Barley and Yak Germplasm Resources and Genetic Improvement, and Institute of Animal Husbandry and Veterinary Medicine, Tibet Academy of Agricultural and Animal Husbandry Sciences, Lhasa, 850009, China.
Jing FengState Key Laboratory of Hulless Barley and Yak Germplasm Resources and Genetic Improvement, and Institute of Animal Husbandry and Veterinary Medicine, Tibet Academy of Agricultural and Animal Husbandry Sciences, Lhasa, 850009, China.
Dongxu WenState Key Laboratory of Hulless Barley and Yak Germplasm Resources and Genetic Improvement, and Institute of Animal Husbandry and Veterinary Medicine, Tibet Academy of Agricultural and Animal Husbandry Sciences, Lhasa, 850009, China.
Hongzhuang WangState Key Laboratory of Hulless Barley and Yak Germplasm Resources and Genetic Improvement, and Institute of Animal Husbandry and Veterinary Medicine, Tibet Academy of Agricultural and Animal Husbandry Sciences, Lhasa, 850009, China.
Sijia LuCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
Kun LiCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
Rizwana SultanDepartment of Pathology, Faculty of Veterinary Science, Cholistan University of Veterinary and Animal Sciences (CUVAS), Bahawalpur, Pakistan.
Bin LiState Key Laboratory of Hulless Barley and Yak Germplasm Resources and Genetic Improvement, and Institute of Animal Husbandry and Veterinary Medicine, Tibet Academy of Agricultural and Animal Husbandry Sciences, Lhasa, 850009, China. xukesuolibin@163.com.

Funding

Natural Science Foundation Project of Tibet Autonomous Region XZ202401ZR0125
6 · The paper itself

Abstract

This study reports the isolation and characterization of Bacillus subtilis K35-1, a novel cellulolytic strain with exceptional forage degradation capabilities. From eight B. subtilis isolates obtained from yak rumen fluid through Congo red screening (hydrolysis capacity = 2.61 ± 0.23), K35-1 demonstrated superior enzymatic performance, achieving peak cellulase (77.26 U/mL) and hemicellulase (222.85 nmol/min/mL) activities at 36 h of fermentation. The whole genome sequencing revealed a 4.06 Mb circular chromosome (GC content 43.83%) encoding 3,980 protein-coding sequences. Comprehensive CAZy annotation identified 703 carbohydrate-active enzymes, including: 87 cellulases spanning 7 GH families (GH5, GH6, GH9, GH12, GH44, GH45, GH48) and 34 hemicellulases from 4 GH families (GH10, GH11, GH26, GH30). Comparative genomic analysis showed K35-1 possesses 40% more glycoside hydrolases than reference strains (Srivastava et al., Mol Genet Genomics 298:361-74, 2023), explaining its enhanced degradation efficiency (53.2% cellulose reduction vs. 7.3% in conventional treatments). Functional annotation revealed: 275 carbohydrate metabolism genes (KEGG), 228 cell wall/membrane biogenesis genes (COG) and 53.91% reduced-virulence mutations (PHI database). The strain's robust enzymatic profile, coupled with minimal antibiotic resistance (11 genes, including ermB), positions K35-1 as both an efficient forage degrader and safe probiotic candidate. These findings provide a genomic foundation for developing novel feed additives to improve livestock nutrition.

Indexed as

Bacillus subtilisCelluloseGenome, BacterialWhole Genome SequencingAnimal FeedAnimalsBacterial ProteinsCattleCellulaseCellulasesFermentationGlycoside HydrolasesPhylogenyRumenBacterial ProteinsCellulaseCellulasesCelluloseGlycoside HydrolaseshemicellulaseBacillus subtilisCellulose degrading bacteriaWhole genome

Identifiers

PMID40713485
PMCPMC12291304

What OpenQuestion holds

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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.