# Probiotic characterization and spore production optimization of Lysinibacillus sp. MK212927

**Authors:** Sayed E. El-Sayed, Albeir A. Messiha

PMC · DOI: 10.1007/s00253-026-13755-8 · Applied Microbiology and Biotechnology · 2026-03-08

## TL;DR

A soil-derived Lysinibacillus strain shows strong probiotic potential, including pathogen inhibition and stress tolerance, and can be optimized for industrial use.

## Contribution

Optimized spore production and comprehensive safety and functional characterization of Lysinibacillus sp. MK212927 as a novel probiotic candidate.

## Key findings

- Lysinibacillus sp. MK212927 inhibits multiple human enteropathogens and survives harsh gastrointestinal conditions.
- Optimized production conditions increased biomass by 3.1-fold and spore yield by 5.4-fold.
- In vivo testing showed improved body weight gain in rats, supporting its use as a feed supplement.

## Abstract

Members of the genus Lysinibacillus are increasingly explored as probiotic candidates, yet thorough screening and safety assessment remain essential due to the toxin-producing potential of related species. In this study, a soil-derived isolate, Lysinibacillus sp. MK212927 demonstrated strong antagonistic activity against multiple human enteropathogens and was selected for comprehensive characterization. The strain exhibited high resilience under physiologically relevant stress conditions, including low pH, simulated gastric and intestinal fluids, bile salts, and thermal exposure. It also displayed desirable probiotic attributes such as antioxidant capacity and bile salt hydrolase activity. Safety evaluation revealed the absence of hemolytic activity, minimal cytotoxicity toward Caco-2 cells, and susceptibility to vancomycin, levofloxacin, sulfamethoxazole, and doxycycline, with intermediate susceptibility to azithromycin and amoxicillin, suggesting a lack of plasmids or mobile genetic elements. To enhance its industrial applicability, response surface methodology (RSM) was applied to optimize biomass and spore production. Optimal conditions (pH 6.1, 33.5 °C, 200 rpm, and 0.21 vvm aeration) resulted in a 3.1-fold increase in biomass and a 5.4-fold increase in spore yield. In vivo assessment further showed that administration of Lysinibacillus sp. MK212927 improved body weight gain in rats, supporting its functional benefits as a feed supplement. Overall, the comprehensive phenotypic and safety evaluations highlight Lysinibacillus sp. MK212927 as a robust probiotic candidate with significant potential for controlling enteropathogens and for use in animal and human nutrition, warranting further preclinical and functional development.

• Lysinibacillus sp. MK212927 exhibits strong inhibitory activity against human enteropathogens.

• The strain tolerates low pH, bile salts, gastric and intestinal fluids, and heat, while displaying antioxidant and bile salt hydrolase activity.

• Optimization of biomass and spore production, along with improved body weight in rats, supports its potential as a feed supplement.

The online version contains supplementary material available at 10.1007/s00253-026-13755-8.

## Linked entities

- **Chemicals:** vancomycin (PubChem CID 14969), levofloxacin (PubChem CID 149096), sulfamethoxazole (PubChem CID 5329), doxycycline (PubChem CID 54671203), azithromycin (PubChem CID 447043), amoxicillin (PubChem CID 33613)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** diarrheal diseases (MESH:D004403), colon cancer (MESH:D015179), infection (MESH:D007239), bacteremia (MESH:D016470), cytotoxic (MESH:D064420), weight loss (MESH:D015431), enteric infection (MESH:D004751), SGF (MESH:D013272), systemic (MESH:D015619), SIF (MESH:D007410), inflammation (MESH:D007249), anorexia (MESH:D000855), weight gain (MESH:D015430), diarrhea (MESH:D003967), Hemolytic (MESH:D006461)
- **Chemicals:** CCK-8 (-), hydrogen peroxide (MESH:D006861), sulfamethoxazole (MESH:D013420), bile acid (MESH:D001647), glycerol (MESH:D005990), Co2+ (MESH:D002245), sucrose (MESH:D013395), sodium acetate (MESH:D019346), PBS (MESH:D007854), Glucose (MESH:D005947), reactive oxygen species (MESH:D017382), doxycycline (MESH:D004318), azithromycin (MESH:D017963), NaCl (MESH:D012965), acid (MESH:D000143), phosphate (MESH:D010710), lactic acid (MESH:D019344), DPPH (MESH:C004931), agar (MESH:D000362), monosaccharides (MESH:D009005), streptomycin (MESH:D013307), vancomycin (MESH:D014640), levofloxacin (MESH:D064704), TSA (MESH:C481298), L-ascorbic acid (MESH:D001205), amoxicillin (MESH:D000658), cholesterol (MESH:D002784), oxytetracycline (MESH:D010118), NaOH (MESH:D012972)
- **Species:** Shouchella clausii (species) [taxon 79880], Komagataella phaffii GS115 (strain) [taxon 644223], Rattus norvegicus (brown rat, species) [taxon 10116], Leptospira sp. AB (species) [taxon 103236], Staphylococcus aureus (species) [taxon 1280], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Lactococcus (lactic streptococci, genus) [taxon 1357], Bifidobacterium (genus) [taxon 1678], Clostridium perfringens ATCC 13124 (strain) [taxon 195103], Homo sapiens (human, species) [taxon 9606], Bacillus anthracis (anthrax bacterium, species) [taxon 1392], Lysinibacillus sp. (species) [taxon 1869345], Clostridium perfringens (species) [taxon 1502], Bacillus cereus (species) [taxon 1396], Escherichia coli (E. coli, species) [taxon 562], Heyndrickxia coagulans (species) [taxon 1398], Bacillus subtilis (species) [taxon 1423], Escherichia coli O157:H7 (no rank) [taxon 83334], Mus musculus (house mouse, species) [taxon 10090], Aspergillus niger (species) [taxon 5061], Lacticaseibacillus rhamnosus GG (strain) [taxon 568703], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Salmonella enterica subsp. enterica serovar Enteritidis (no rank) [taxon 149539], Bacillus licheniformis (species) [taxon 1402], Campylobacter jejuni (species) [taxon 197], Lactobacillus acidophilus (species) [taxon 1579], Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371]
- **Mutations:** C-100  C, C for 24-48, C250R
- **Cell lines:** MK212927 — Macaca fascicularis (Crab-eating macaque), Spontaneously immortalized cell line (CVCL_3631), Caco-2 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0025), ATCC 13124 — Homo sapiens (Human), Transformed cell line (CVCL_9Y27), 13076 — Homo sapiens (Human), Amyotrophic lateral sclerosis, Transformed cell line (CVCL_IL99), ATCC 29213 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), ATCC 14028 — Homo sapiens (Human), Transformed cell line (CVCL_FD91)

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## References

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Source: https://tomesphere.com/paper/PMC12971817