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Taxonomy of fungal complex causing red-skin root of Panax ginseng in China
Xiao H. Lu,Xi M. Zhang,Xiao L. Jiao,Jianjun J. Hao,Xue S. Zhang,Yi Luo,Wei W. Gao 고려인삼학회 2020 Journal of Ginseng Research Vol.44 No.3
Background: Red-skin root of Asian ginseng (Panax ginseng) significantly reduces the quality and limits theproduction of ginseng in China. The disease has long been thought to be a noninfectious physiologicaldisease, except one report that proved itwas an infectious disease. However, the causal agents have not beensuccessfully determined. In the present study, we were to reveal the pathogens that cause red-skin disease. Methods: Ginseng roots with red-skin root symptoms were collected from commercial fields in NortheastChina. Fungi were isolated from the lesion and identified based on morphological characters alongwith multilocus sequence analyses on internal transcription spacer, b-tubulin (tub2), histone H3 (his3),and translation elongation factor 1a (tef-1a). Pathogens were confirmed by inoculating the isolates inginseng roots. Results: A total of 230 isolates were obtained from 209 disease samples. These isolates were classifiedinto 12 species, including Dactylonectria sp., D. hordeicola, Fusarium acuminatum, F. avenaceum, F. solani,F. torulosum, Ilyonectria mors-panacis, I. robusta, Rhexocercosporidium panacis, and three novel speciesI. changbaiensis, I. communis, and I. qitaiheensis. Among them, I. communis, I. robusta, and F. solani had thehighest isolation frequencies, being 36.1%, 20.9%, and 23.9%, respectively. All these species isolated werepathogenic to ginseng roots and caused red-skin root disease under appropriate condition. Conclusion: Fungal complex is the causal agent of red-skin root in P. ginseng.
Taxonomy of fungal complex causing red-skin root of Panax ginseng in China
Lu, Xiao H.,Zhang, Xi M.,Jiao, Xiao L.,Hao, Jianjun J.,Zhang, Xue S.,Luo, Yi,Gao, Wei W. The Korean Society of Ginseng 2020 Journal of Ginseng Research Vol.44 No.3
Background: Red-skin root of Asian ginseng (Panax ginseng) significantly reduces the quality and limits the production of ginseng in China. The disease has long been thought to be a noninfectious physiological disease, except one report that proved it was an infectious disease. However, the causal agents have not been successfully determined. In the present study, we were to reveal the pathogens that cause red-skin disease. Methods: Ginseng roots with red-skin root symptoms were collected from commercial fields in Northeast China. Fungi were isolated from the lesion and identified based on morphological characters along with multilocus sequence analyses on internal transcription spacer, β-tubulin (tub2), histone H3 (his3), and translation elongation factor 1α (tef-1α). Pathogens were confirmed by inoculating the isolates in ginseng roots. Results: A total of 230 isolates were obtained from 209 disease samples. These isolates were classified into 12 species, including Dactylonectria sp., D. hordeicola, Fusarium acuminatum, F. avenaceum, F. solani, F. torulosum, Ilyonectria mors-panacis, I. robusta, Rhexocercosporidium panacis, and three novel species I. changbaiensis, I. communis, and I. qitaiheensis. Among them, I. communis, I. robusta, and F. solani had the highest isolation frequencies, being 36.1%, 20.9%, and 23.9%, respectively. All these species isolated were pathogenic to ginseng roots and caused red-skin root disease under appropriate condition. Conclusion: Fungal complex is the causal agent of red-skin root in P. ginseng.
Insights into the removal of gaseous oxytetracycline by combined ozone and membrane biofilm reactor
Z.S. Wei,X.L. Chen,Z.S. Huang,H.Y. Jiao,X.L. Xiao 대한환경공학회 2022 Environmental Engineering Research Vol.27 No.6
Gaseous emerging organic compounds (GEOCs) may harm human health and ecological environment. High temperature composting of livestock manure may produce oxytetracycline (OTC) waste gas. Here, we investigated treatment OTC in waste gas by combined ozone and membrane biofilm reactor (MBfR) with desulphurizing bacteria. The performance, the microbial community, gene function and the mechanism for OTC removal in the ozone-MBfR were evaluated. The ozone-MBfR system could achieve more degradation of OTC completely than MBfR. Desulfovibrio, Lentimicrobium, Aminivibrio, Thioalkalispira, Erysipelothrix, Mangroviflexus, Azoarcus, Thauera, Geobacter, Paracoccus, and Dethiosulfatibacter were the dominant genera. Pseudomonas, Escherichia, Bacteroides, Salmonella, Paracoccus, Stappia were contribution to OTC degradation. With the addition of ozone, the community diversity increased; some genera, such as Tenericutes- uncultured, and Desulfovibrio, increased in abundance, whereas others, such as Thauera, and Petrimonas, decreased. Ozone destroyed the enol structure in OTC molecular structure and produces biodegradable products, ozone oxidation was combined with biodegradation, to achieve thoroughly degrade OTC in waste gas. The novel hybrid ozone-MBfR is a cost-effective and robust alternative to GEOCs treatment.
P. Z. Si,X. L. Wang,X. F. Xiao,H. J. Chen,X. Y. Liu,L. Jiang,J. J. Liu,Z. W. Jiao,H. L. Ge 한국자기학회 2015 Journal of Magnetics Vol.20 No.3
Cr₂O₃ nanoparticles were prepared via one-step reactive laser ablation of Cr in oxygen. The metastable CrO₂ phase was obtained through the subsequent oxidation of Cr₂O₃ nanoparticles under O₂ with gas pressures of up to 40 MPa. The as-prepared Cr₂O₃ nanoparticles are spherical or rectangular in shape with sizes ranging from 20 nm to 50 nm. High oxygen pressure annealing is effective in producing meta-stable CrO₂ from as-dried Cr₂O₃ nanoparticles, and the Cr₂O₃ nanoparticles exhibit a weak ferromagnetic behavior with an exchange bias of up to 11 mT that can be ascribed to the interfacial exchange coupling between uncompensated surface spins and the antiferromagnetic core. The Cr₂O₃/CrO₂ nanoparticles exhibit an enhanced saturation magnetization and a reduced exchange bias with an increasing faction of CrO₂ due to the elimination of uncompensated surface spins over the Cr₂O₃ nanoparticles when exposed to a high pressure of O₂ and/or possible phase segregation that results in a smaller grain size for both Cr₂O₃ and CrO₂.