Skip to content
DraconiticResearch
Search Sources API
210,049 studies31 sourcesUpdated 7 min ago
Peer-reviewedCC BY 4.0PeerJ

Extracellular amylolytic activity in marine Croceibacter sp. 23-6: Cu ²⁺ response and optimized wheat starch hydrolysis

  1. 1Tropical Biodiversity and Bioresource Utilization Laboratory, Qiongtai Normal University, Haikou, China
  2. 2Sanya Key Laboratory for Breeding of Tropical Crops, Hainan Tropical Ocean University, Sanya, China

Abstract

Background: Marine bacteria are important sources of extracellular hydrolytic enzymes, but the amylolytic activity of many non-model marine bacterial lineages remains insufficiently characterized at the phenotype level. This study evaluated extracellular amylolytic activity in the marine isolate Croceibacter sp. 23-6 and examined its metal-ion response and wheat starch hydrolysis performance under defined laboratory conditions.

Methods: Strain 23-6 was isolated from mesopelagic seawater of the western Pacific Ocean and identified at the genus level using 16S rRNA gene sequence analysis. Extracellular amylolytic activity was first screened on starch agar. A partially purified extracellular amylolytic protein preparation was then used to determine the effects of temperature, pH, thermal and pH stability, metal ions, apparent kinetic parameters and hydrolysis of different starch substrates. Wheat starch hydrolysis was further evaluated using single-factor experiments and response surface methodology based on a Box–Behnken design.

Results: Strain 23-6 produced a clear starch-hydrolysis halo and was conservatively assigned to the genus Croceibacter . The partially purified extracellular protein fraction showed maximum amylolytic activity at 50 °C and pH 7.0 and retained comparatively higher activity under near-neutral conditions. Among the tested metal ions, Cu ²⁺ increased the measured relative activity to 119.0% at 3 mM, whereas K ⁺ , Mn ²⁺ , Zn ²⁺ and Fe ²⁺ decreased the measured activity. Wheat starch showed the highest relative reducing-sugar release among the tested insoluble starch substrates. Response surface optimization predicted suitable hydrolysis conditions of approximately 52 min, 50 °C, 4.0 U/mL enzyme and 1.0% wheat starch. Validation under the adjusted conditions yielded 2.43 ± 0.09 mg/mL reducing sugars, expressed as maltose equivalents, consistent with the model prediction.

Conclusions: These results provide strain-level evidence that Croceibacter sp. 23-6 exhibits extracellular amylolytic activity and indicate that its partially purified extracellular protein fraction displays a measurable Cu ²⁺ -responsive activity profile and wheat starch hydrolysis capacity. The findings define the functional properties of this marine bacterial extracellular amylolytic fraction while leaving the identity of the responsible enzyme(s), preparation homogeneity, and the mechanism of Cu ²⁺ response for future work.

Related

  1. Synergistic Alcalase-papain hydrolysis of egg white protein: enhancing structural unfolding, antioxidant activity, and gastrointestinal stability.
    Jialei Shi, Xianzhen Li, Xunyu Song +1
    Food chemistry: XPeer-reviewedCC BYFull textMolecular biology & gene regulationEurope PMC
  2. From mucosal activity to medicinal products: translational evidence for Akkermansia muciniphila extracellular vesicles
    Quanli Zhu, Yingchao Liu, Yu Song
    Frontiers in ImmunologyPeer-reviewedCC BY 4.0Full textMolecular biology & gene regulationCrossref
  3. Standardized Microplate‐Based Assays for Quantifying Antioxidant Activity in Extracellular Vesicles and Nanovesicles Across Biological Kingdoms
    Juan Antonio Nieto, María‐Carmen López de las Hazas, Victoria Martín‐Santiago +13
    Journal of extracellular vesiclesPeer-reviewedCC BYFull textMolecular biology & gene regulationEurope PMCPMC
  4. Specific residues modulate the antiviral activity of the extracellular vesicle-derived effector SH3b domain from Lactobacillus johnsonii N6.2
    Asra B. Sharjeel, Javier Rosero, Chantal Ronacher +3
    Frontiers in ImmunologyPeer-reviewedCC BY 4.0Full textMolecular biology & gene regulationCrossrefPMC
  5. Human thymic Treg-derived extracellular vesicles display a defined proteomic and miRNA signature with donor-variable suppressive activity.
    Marta Fernández-Castillo, Elena Blázquez-López, Esther Bernaldo-de-Quiros +7
    Molecular medicine (Cambridge, Mass.)Peer-reviewedCC BYFull textMolecular biology & gene regulationEurope PMCPMC
BibTeX
@article{jiang2026extracellular,
  title = {{Extracellular amylolytic activity in marine Croceibacter sp. 23-6: Cu ²⁺ response and optimized wheat starch hydrolysis}},
  author = {Fangyan Jiang and Yuanyuan Zhang and Hongjin Zhang and Xiuqing Lin and Xiaoxiong Xu and Huimin Feng},
  journal = {PeerJ},
  year = {2026},
  month = nov,
  doi = {10.7717/peerj.21854},
  url = {https://peerj.com/articles/21854},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Extracellular amylolytic activity in marine Croceibacter sp. 23-6: Cu ²⁺ response and optimized wheat starch hydrolysis
AU  - Fangyan Jiang
AU  - Yuanyuan Zhang
AU  - Hongjin Zhang
AU  - Xiuqing Lin
AU  - Xiaoxiong Xu
AU  - Huimin Feng
PY  - 2026
DA  - 2026/11/03
JO  - PeerJ
DO  - 10.7717/peerj.21854
UR  - https://peerj.com/articles/21854
AB  - Background: Marine bacteria are important sources of extracellular hydrolytic enzymes, but the amylolytic activity of many non-model marine bacterial lineages remains insufficiently characterized at the phenotype level. This study evaluated extracellular amylolytic activity in the marine isolate Croceibacter sp. 23-6 and examined its metal-ion response and wheat starch hydrolysis performance under defined laboratory conditions.  Methods: Strain 23-6 was isolated from mesopelagic seawater of the western Pacific Ocean and identified at the genus level using 16S rRNA gene sequence analysis. Extracellular amylolytic activity was first screened on starch agar. A partially purified extracellular amylolytic protein preparation was then used to determine the effects of temperature, pH, thermal and pH stability, metal ions, apparent kinetic parameters and hydrolysis of different starch substrates. Wheat starch hydrolysis was further evaluated using single-factor experiments and response surface methodology based on a Box–Behnken design.  Results: Strain 23-6 produced a clear starch-hydrolysis halo and was conservatively assigned to the genus Croceibacter . The partially purified extracellular protein fraction showed maximum amylolytic activity at 50 °C and pH 7.0 and retained comparatively higher activity under near-neutral conditions. Among the tested metal ions, Cu ²⁺ increased the measured relative activity to 119.0% at 3 mM, whereas K ⁺ , Mn ²⁺ , Zn ²⁺ and Fe ²⁺ decreased the measured activity. Wheat starch showed the highest relative reducing-sugar release among the tested insoluble starch substrates. Response surface optimization predicted suitable hydrolysis conditions of approximately 52 min, 50 °C, 4.0 U/mL enzyme and 1.0% wheat starch. Validation under the adjusted conditions yielded 2.43 ± 0.09 mg/mL reducing sugars, expressed as maltose equivalents, consistent with the model prediction.  Conclusions: These results provide strain-level evidence that Croceibacter sp. 23-6 exhibits extracellular amylolytic activity and indicate that its partially purified extracellular protein fraction displays a measurable Cu ²⁺ -responsive activity profile and wheat starch hydrolysis capacity. The findings define the functional properties of this marine bacterial extracellular amylolytic fraction while leaving the identity of the responsible enzyme(s), preparation homogeneity, and the mechanism of Cu ²⁺ response for future work.
SN  - 2167-8359
ER  -