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1.
Front Microbiol ; 15: 1367043, 2024.
Article in English | MEDLINE | ID: mdl-38737412

ABSTRACT

The identification of microorganisms with excellent flocculants-producing capability and optimization of the fermentation process are necessary for the wide-scale application of bioflocculants. Therefore, we isolated and identified a highly efficient flocculation performance strain of Stenotrophomonas pavanii GXUN74707 from the sludge. The optimal fermentation and flocculation conditions of strain S. pavanii GXUN74707 was in fermentation medium with glucose and urea as the carbon and nitrogen sources, respectively, at pH 7.0 for 36 h, which treatment of kaolin suspension with 0.5 mL of the fermentation broth resulted in a flocculation rate of 99.0%. The bioflocculant synthesized by strain S. pavanii GXUN74707 was found mainly in the supernatant of the fermentation broth. Chemical analysis revealed that the pure bioflocculant consisted of 79.70% carbohydrates and 14.38% proteins. The monosaccharide components of MBF-GXUN74707 are mainly mannose (5.96 µg/mg), galactose (1.86 µg/mg), and glucose (1.73 µg/mg). Infrared spectrometric analysis showed the presence of carboxyl (COO-), hydroxyl (-OH) groups. The SEM images showed clumps of rod-shaped bacteria with adhesion of extracellular products. Furthermore, the strain decolored dye wastewater containing direct black, direct blue, and Congo red by 89.2%, 95.1%, 94.1%, respectively. The chemical oxygen demand (COD) and biological oxygen demand (BOD) removal rates after treatment of aquaculture wastewater with the fermentation broth were 68% and 23%, respectively. This study is the first to report the performance and application of strain Stenotrophomonas pavanii in wastewater flocculation. The results indicate that strain S. pavanii is a good candidate for the production novel bioflocculants and demonstrates its potential industrial practicality in biotechnology processes.

2.
Mitochondrial DNA B Resour ; 7(7): 1211-1212, 2022.
Article in English | MEDLINE | ID: mdl-35814183

ABSTRACT

Sloanea hemsleyana is a potential commercial and oil tree species. This study is the first to report and analyze complete chloroplast genome sequences of S. hemsleyana as a genomic resource for conservation purposes. The chloroplast genome is 158,085 bp in length and consisted of a large single-copy (LSC) region (88,446 bp), and a small single-copy (SSC) region (17,659 bp), separated by a pair of inverted repeats (IR) regions (25,990 bp). It contains 108 genes, with 74 protein-coding genes, 30 tRNA genes, and 4 rRNA genes. Phylogenetic analysis revealed that S. hemsleyana was most closely related to S. sinensis.

3.
J Trace Elem Med Biol ; 65: 126721, 2021 May.
Article in English | MEDLINE | ID: mdl-33508548

ABSTRACT

BACKGROUND: Excess copper (Cu) is an oxidative stress factor which associates with a variety of diseases. The aim of this study was to evaluate the effect of Cu in primary chicken embryo hepatocytes (CEHs). METHODS: CEHs were isolated from 13 days old chicken embryos and followed by different concentration Cu (0, 10, 100, 200 µM) and/or ALC treatment (0.3 mg/mL) for 12 or 24 h. The effects of Cu exposure in CEHs were determined by detecting reactive oxygen species (ROS), malondialdehyde (MDA), mitochondrial membrane potential (MMP), and ATP levels. The expression of mitochondrial dynamics-related genes and proteins were also detected. RESULTS: Results showed that Cu treatment (100 or 200 µM) significantly decreased CEHs viability, MMP and ATP levels, increased ROS and MDA levels in 12 or 24 h. The up-regulated mitochondrial fission genes and protein in 100 and 200 µM Cu groups suggested Cu promoted mitochondrial division but not fusion. However, the co-treatment of ALC and Cu alleviated those changes compared with the 100 or 200 µM Cu groups. CONCLUSION: In conclusion, we speculated that Cu increased the oxidative stress and induced mitochondria dysfunction via disturbing mitochondrial dynamic balance in CEHs, and this process was not completely reversible.


Subject(s)
Copper Sulfate/pharmacology , Hepatocytes/drug effects , Mitochondrial Dynamics/drug effects , Animals , Cell Survival/drug effects , Chick Embryo , Chickens , Dose-Response Relationship, Drug , Hepatocytes/metabolism , Malondialdehyde/analysis , Malondialdehyde/metabolism , Mitochondria/drug effects , Mitochondria/metabolism , Oxidative Stress/drug effects , Reactive Oxygen Species/analysis , Reactive Oxygen Species/metabolism
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