47 citations as recorded by crossref.

1. Transition of the Bacterial Community and Culturable Chitinolytic Bacteria in Chitin-treated Upland Soil: From <i>Streptomyces</i> to Methionine-auxotrophic <i>Lysobacter</i> and Other Genera Y. Iwasaki et al. https://doi.org/10.1264/jsme2.ME19070
2. Changes in bacterial community structure and carbon metabolism in sandy soil under the long-term application of chitin-rich organic material and attapulgite H. Zhang et al. https://doi.org/10.1016/j.apsoil.2023.105161
3. Long-term organic amendments regulate cbbL-harboring bacterial community via soil physicochemical properties and enzyme activities in a paddy soil J. Xu et al. https://doi.org/10.1007/s11368-026-04244-6
4. Chitin degradation and the temporary response of bacterial chitinolytic communities to chitin amendment in soil under different fertilization regimes C. Hui et al. https://doi.org/10.1016/j.scitotenv.2019.136003
5. Contrasting response strategies of microbial functional traits to polycyclic aromatic hydrocarbons contamination under aerobic and anaerobic conditions Y. Zhu et al. https://doi.org/10.1016/j.jhazmat.2023.131548
6. Challenges and Limitations in Soil Enzymology P. Nannipieri & L. Giagnoni https://doi.org/10.1007/s42729-026-03438-8
7. Influence of biochar and biochar-based fertilizer on yield, quality of tea and microbial community in an acid tea orchard soil W. Yang et al. https://doi.org/10.1016/j.apsoil.2021.104005
8. Statement concerning the review of the approval of the basic substances chitosan and chitosan hydrochloride when used in plant protection T. Coja et al. https://doi.org/10.2903/j.efsa.2025.9318
9. Short-Term Application of Magnesium Fertilizer Affected Soil Microbial Biomass, Activity, and Community Structure W. Yang et al. https://doi.org/10.1007/s42729-020-00392-x
10. Chitosan degradation and associated changes in bacterial community structures in two contrasting soils A. Sawaguchi et al. https://doi.org/10.1080/00380768.2014.1003965
11. Linking Chitin Degradation to Arsenic Methylation under Oxic Conditions: A Critical Driver of Arsenic Cycling in Paddy Soils G. Chen et al. https://doi.org/10.1021/acs.est.5c00970
12. Carbohydrate Hydrolytic Potential and Redundancy of an Anaerobic Digestion Microbiome Exposed to Acidosis, as Uncovered by Metagenomics M. Bertucci et al. https://doi.org/10.1128/AEM.00895-19
13. Changes in Soil Bacteriobiome in Response to Organic Amendments and Cd2+ Stress A. Borowik et al. https://doi.org/10.3390/ijms27135783
14. Bacterial Communities in the Fruiting Bodies and Background Soils of the White Truffle Tuber magnatum F. Sillo et al. https://doi.org/10.3389/fmicb.2022.864434
15. A bio-based supramolecular hydrogel with gel-sol transition for intelligent and sustainable agro-chemical delivery L. Li et al. https://doi.org/10.1016/j.cej.2026.173898
16. Sludge-derived hydrothermal carbonization aqueous phase regulates agro-ecosystem multifunctionality by affecting cross-trophic community in periphyton X. Zhong et al. https://doi.org/10.48130/aee-0025-0012
17. Analysis of chitinase diversity in the Baltic Sea bottom sediments A. Teplyuk et al. https://doi.org/10.1134/S0026261717010131
18. Close neighbors, not intruders: investigating the role of tank bromeliads in shaping faunal microbiomes R. Martínez-Mota et al. https://doi.org/10.7717/peerj.19376
19. Functional Reorganization of Microbial Decomposers Drives Differentiation in Dead Biomass Degradation During Plantation Development X. Zuo et al. https://doi.org/10.3390/f17020223
20. Fabrication of stimuli gated nanoformulation for site-specific delivery of thymoquinone for colon cancer treatment – Insight into thymoquinone’s improved physicochemical properties J. Pushpa Sweety et al. https://doi.org/10.1016/j.jddst.2019.101334
21. Cicada necrobiome mediates greenhouse and trace gas pulses following periodic mass emergence M. Purchase et al. https://doi.org/10.1016/j.apsoil.2026.106813
22. Ecological Functions of Agricultural Soil Bacteria and Microeukaryotes in Chitin Degradation: A Case Study A. Wieczorek et al. https://doi.org/10.3389/fmicb.2019.01293
23. A novel lytic polysaccharide monooxygenase from enrichment microbiota and its application for shrimp shell powder biodegradation Y. Zhang et al. https://doi.org/10.3389/fmicb.2023.1097492
24. Effects of chitin degradation products N-acetylglucosamine and N,Nʹ-diacetylchitobiose on chitinase activity and bacterial community structure in an incubated upland soil Y. Shimoi et al. https://doi.org/10.1080/00380768.2020.1767488
25. Organic Farming Improves Soil Microbial Abundance and Diversity under Greenhouse Condition: A Case Study in Shanghai (Eastern China) J. Liao et al. https://doi.org/10.3390/su10103825
26. Functional metagenomics reveals differential chitin degradation and utilization features across free-living and host-associated marine microbiomes I. Raimundo et al. https://doi.org/10.1186/s40168-020-00970-2
27. Planctomycetes of the Genus Singulisphaera Possess Chitinolytic Capabilities A. Ivanova et al. https://doi.org/10.3390/microorganisms12071266
28. Microbial inoculants with straw mediate degradation-level-specific changes in soil carbon cycling genes and microbial community Y. Han et al. https://doi.org/10.1186/s40793-026-00898-4
29. Genome sequencing and analysis of the first spontaneous Nanosilver resistant bacterium Proteus mirabilis strain SCDR1 A. Saeb et al. https://doi.org/10.1186/s13756-017-0277-x
30. Preliminary Study on the Biodegradability of Chitosan Films Emulsified with Palm Oils (Aracaceae) from the Brazilian Cerrado A. Reis & S. Arrudas https://doi.org/10.6000/1929-5995.2020.09.06
31. Paludicola psychrotolerans gen. nov., sp. nov., a novel psychrotolerant chitinolytic anaerobe of the family Ruminococcaceae Y. Li et al. https://doi.org/10.1099/ijsem.0.002260
32. Redox-Related Metabolic Dynamics Imprinted on Short-Chain Carboxylic Acids in Soil Water Extracts: A 13C-Exometabolomics Analysis B. Hassanpour & L. Aristilde https://doi.org/10.1021/acs.estlett.0c00922
33. Activity‐Based Protein Profiling of Chitin Catabolism E. Zegeye et al. https://doi.org/10.1002/cbic.202000616
34. Genome Analysis of Fimbriiglobus ruber SP5T, a Planctomycete with Confirmed Chitinolytic Capability N. Ravin et al. https://doi.org/10.1128/AEM.02645-17
35. Enhancing the Anti-biofouling Properties of Polyethersulfone Membrane Using Chitosan-Powder Activated Carbon Composite H. Gafri et al. https://doi.org/10.1007/s10924-019-01505-z
36. The Stimulatory Effects of Nanochitin Whisker on Carbon and Nitrogen Metabolism and on the Enhancement of Grain Yield and Crude Protein of Winter Wheat Y. Cheng et al. https://doi.org/10.3390/molecules24091752
37. Recent advances in the bioprospection and applications of chitinolytic bacteria for valorization of waste chitin N. Dhole et al. https://doi.org/10.1007/s00203-021-02234-5
38. Effects of the Applications of Chitin and Chitosan on Soil Organisms J. Eo et al. https://doi.org/10.7745/KJSSF.2015.48.2.132
39. Unravelling the regulatory network behind chitin degradation in Serratia marcescens W. Demeester et al. https://doi.org/10.1111/brv.70020
40. Model substrate particles uncover dynamics of microbial communities associated with particulate organic matter decomposition in soil E. Simon et al. https://doi.org/10.1093/ismeco/ycag044
41. The composition, localization and function of low-temperature-adapted microbial communities involved in methanogenic degradations of cellulose and chitin from Qinghai-Tibetan Plateau wetland soils Y. Dai et al. https://doi.org/10.1111/jam.13164
42. Environmental toxicity and biodegradation of chitosan derivatives: A comprehensive review I. Koumentakou et al. https://doi.org/10.1016/j.jiec.2024.11.027
43. Differential response of chitinolytic and proteolytic depolymerization-mineralization pathways to organic nitrogen substrates C. Kasmerchak et al. https://doi.org/10.1007/s00374-025-01932-2
44. Selenium combined with chitin reduced phosphorus leaching in soil with pomelo by driving soil phosphorus cycle via microbial community Y. Tang et al. https://doi.org/10.1016/j.jece.2021.107060
45. Microbial carbon use efficiency during plant residue decomposition: Integrating multi-enzyme stoichiometry and C balance approach B. Agumas et al. https://doi.org/10.1016/j.apsoil.2020.103820
46. Thermogravimetric evaluation of chitin degradation in soil: implication for the enhancement of ammonification of native organic nitrogen by chitin addition Y. Kumeta et al. https://doi.org/10.1080/00380768.2018.1457408
47. Microbial Succession of Anaerobic Chitin Degradation in Freshwater Sediments S. Wörner et al. https://doi.org/10.1128/AEM.00963-19