scholarly journals Influence of spreading cultivation with food waste culture medium on the degradation of organophosphorus pesticides by a microbial consortium OP-1

2016 ◽  
Vol 42 (4) ◽  
Author(s):  
Youchi Zhang ◽  
Xiaojun Jin ◽  
Wensui Luo
2018 ◽  
Vol 11 (6) ◽  
pp. 1124-1136 ◽  
Author(s):  
Caihong Song ◽  
Yali Zhang ◽  
Xunfeng Xia ◽  
Hui Qi ◽  
Mingxiao Li ◽  
...  

2018 ◽  
Vol 259 ◽  
pp. 1-9 ◽  
Author(s):  
Caihong Song ◽  
Mingxiao Li ◽  
Hui Qi ◽  
Yali Zhang ◽  
Dongming Liu ◽  
...  

Fermentation ◽  
2019 ◽  
Vol 5 (4) ◽  
pp. 98 ◽  
Author(s):  
Nathan D. Schwalm ◽  
Wais Mojadedi ◽  
Elliot S. Gerlach ◽  
Marcus Benyamin ◽  
Matthew A. Perisin ◽  
...  

Food waste disposal and transportation of commodity chemicals to the point-of-need are substantial challenges in military environments. Here, we propose addressing these challenges via the design of a microbial consortium for the fermentation of food waste to hydrogen. First, we simulated the exchange metabolic fluxes of monocultures and pairwise co-cultures using genome-scale metabolic models on a food waste proxy. We identified that one of the top hydrogen producing co-cultures comprised Clostridium beijerinckii NCIMB 8052 and Yokenella regensburgei ATCC 43003. A consortium of these two strains produced a similar amount of hydrogen gas and increased butyrate compared to the C. beijerinckii monoculture, when grown on an artificial garbage slurry. Increased butyrate production in the consortium can be attributed to cross-feeding of lactate produced by Y. regensburgei. Moreover, exogenous lactate promotes the growth of C. beijerinckii with or without a limited amount of glucose. Increasing the scale of the consortium fermentation proved challenging, as two distinct attempts to scale-up the enhanced butyrate production resulted in different metabolic profiles than observed in smaller scale fermentations. Though the genome-scale metabolic model simulations provided a useful starting point for the design of microbial consortia to generate value-added products from waste materials, further model refinements based on experimental results are required for more robust predictions.


2021 ◽  
Vol 787 (1) ◽  
pp. 012026
Author(s):  
Qingbo Meng ◽  
Yude Gao ◽  
Shuangke Li ◽  
Bini Jiang ◽  
Mingfei He ◽  
...  

Author(s):  
Mohit Mishra ◽  
Sushma Chauhan ◽  
Balasubramanian Velramar ◽  
Rakesh Kumar Soni ◽  
Sudheer Deva Venkata Narayana Pamidimarri

Author(s):  
Awtar Krishan ◽  
Dora Hsu

Cells exposed to antitumor plant alkaloids, vinblastine and vincristine sulfate have large proteinacious crystals and complexes of ribosomes, helical polyribosomes and electron-dense granular material (ribosomal complexes) in their cytoplasm, Binding of H3-colchicine by the in vivo crystals shows that they contain microtubular proteins. Association of ribosomal complexes with the crystals suggests that these structures may be interrelated.In the present study cultured human leukemic lymphoblasts (CCRF-CEM), were incubated with protein and RNA-synthesis inhibitors, p. fluorophenylalanine, puromycin, cycloheximide or actinomycin-D before the addition of crystal-inducing doses of vinblastine to the culture medium. None of these compounds could completely prevent the formation of the ribosomal complexes or the crystals. However, in cells pre-incubated with puromycin, cycloheximide, or actinomycin-D, a reduction in the number and size of the ribosomal complexes was seen. Large helical polyribosomes were absent in the ribosomal complexes of cells treated with puromycin, while in cells exposed to cycloheximide, there was an apparent reduction in the number of ribosomes associated with the ribosomal complexes (Fig. 2).


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