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1.
Bioprocess Biosyst Eng ; 38(1): 79-84, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25060412

RESUMO

Rubrivivax gelatinosus cultivated in wastewater environment can combine the biomass resource recycling for generating chemicals with sewage purification. However, low biomass accumulation restricts the exertion of this advantage. Thus, this paper investigated Fe(3+) advancement for biomass production in starch wastewater under light-anaerobic condition. Results showed that addition of Fe(3+) was successful in enhancing biomass production, which certainly improved the feasibility of biomass recycling in R. gelatinosus starch wastewater treatment. With optimal Fe(3+) dosage (20 mg/L), biomass production reached 4,060 mg/L, which was 1.63 times that of control group. Amylase activity was improved by 48 %. Both COD removal and starch removal reached 90 %. Hydraulic retention time was shortened by 25 %. Proper Fe(3+) dosage enhanced biomass production, but excess Fe(3+) was harmful for biomass accumulation.


Assuntos
Burkholderiaceae/crescimento & desenvolvimento , Esgotos/microbiologia , Amilases/metabolismo , Análise da Demanda Biológica de Oxigênio , Biomassa , Reatores Biológicos , Compostos Férricos/química , Amido/metabolismo
2.
Water Sci Technol ; 70(12): 1969-75, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25521132

RESUMO

Rubrivivax gelatinosus has the potential of biomass resource recycling combined with sewage purification. However, low biomass production and yield restricts the potential for sewage purification. Thus, this research investigated the improvement of biomass production and yield and organics reduction by Fe(3+) in R. gelatinosus wastewater treatment. Results showed that 10-30 mg/L Fe(3+) improved biomass yield in wastewater to a level found in culture medium. With optimal dosage (20 mg/L), biomass production reached 4,300 mg/L, which was 1.67 times that of the control group. Biomass yield was improved by 43.3%. Chemical oxygen demand (COD) removal reached above 91%. Hydraulic retention time was shortened by 25%. Mechanism analysis indicated that Fe(3+) enhanced the succinate and NADH dehydrogenase activities and, bacteriochlorophyll content in three energy metabolism pathways. These effects then enhanced adenosine triphosphate (ATP) production, which led to more biomass accumulation and COD removal. With 20 mg/L Fe(2+) dosage, succinate and NADH dehydrogenase, coproporphyrinogen III oxidase activities, bacteriochlorophyll content and ATP production were improved, respectively, by 48.4, 50.8, 50, 67 and 56% compared to those of the control group.


Assuntos
Betaproteobacteria/crescimento & desenvolvimento , Biomassa , Ferro/metabolismo , Fotofosforilação , Gerenciamento de Resíduos/métodos , Trifosfato de Adenosina/metabolismo , Bacterioclorofilas/metabolismo , Betaproteobacteria/metabolismo , Reatores Biológicos , Respiração Celular , NADH Desidrogenase/metabolismo , Reciclagem , Esgotos , Succinato Desidrogenase/metabolismo , Águas Residuárias
3.
Environ Technol ; 35(17-20): 2604-9, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25145217

RESUMO

This paper investigated Mg2+ enhancement of biomass production through regulating the generation and use of energy in Rubrivivax gelatinosus wastewater treatment. Results showed that proper Mg2+ dosage range was 1.5-15 mg/L. With optimal Mg2+ dosage (10 mg/L), biomass production (5010 mg/L) was improved by 60%. Both protein and chemical oxygen demand (COD) removals reached above 90%. Biomass yield improved by 38%. Hydraulic retention time was shortened by 25%. Mechanism analysis indicated that as activator, Mg2+ promoted specifically isocitrate dehydrogenase (IDH) and Ca2+ / Mg2+ -ATPase activities in energy metabolism, and then improved the generation of adenosine triphosphate (ATP) and the use of ATP. This enhanced the secretion and activity of protease, protein and COD removals, and then led to more biomass production. With 10 mg/L Mg2+, IDH and Ca2+ / Mg2+ -ATPase activities, ATP production, protease activity were improved by 43.8%, 40.6%, 39.4% and 46.5%, respectively.


Assuntos
Betaproteobacteria/metabolismo , Biomassa , Reatores Biológicos/microbiologia , Águas Residuárias/microbiologia , Purificação da Água/métodos , Trifosfato de Adenosina/metabolismo , Magnésio/metabolismo , Reciclagem
4.
Front Immunol ; 11: 1399, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32733465

RESUMO

Thymic involution is an important factor leading to the aging of the immune system. Most of what we know regarding thymic aging comes from mouse models, and the nature of the thymic aging process in humans remains largely unexplored due to the lack of a model system that permits longitudinal studies of human thymic involution. In this study, we sought to explore the potential to examine human thymic involution in humanized mice, constructed by transplantation of fetal human thymus and CD34+ hematopoietic stem/progenitor cells into immunodeficient mice. In these humanized mice, the human thymic graft first underwent acute recoverable involution caused presumably by transplantation stress, followed by an age-related chronic form of involution. Although both the early recoverable and later age-related thymic involution were associated with a decrease in thymic epithelial cells and recent thymic emigrants, only the latter was associated with an increase in adipose tissue mass in the thymus. Furthermore, human thymic grafts showed a dramatic reduction in FOXN1 and AIRE expression by 10 weeks post-transplantation. This study indicates that human thymus retains its intrinsic mechanisms of aging and susceptibility to stress-induced involution when transplanted into immunodeficient mice, offering a potentially useful in vivo model to study human thymic involution and to test therapeutic interventions.


Assuntos
Envelhecimento/fisiologia , Timo/imunologia , Timo/metabolismo , Animais , Biomarcadores , Movimento Celular , Células Epiteliais/imunologia , Células Epiteliais/metabolismo , Imunofluorescência , Expressão Gênica , Humanos , Imunofenotipagem , Camundongos , Camundongos Transgênicos , Modelos Animais , Reação em Cadeia da Polimerase em Tempo Real , Subpopulações de Linfócitos T/imunologia , Subpopulações de Linfócitos T/metabolismo , Timo/citologia
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