Synthesis of magnetic zwitterionic–hydrophilic material for the selective enrichment of N-linked glycopeptides

2017 ◽  
Vol 1482 ◽  
pp. 23-31 ◽  
Author(s):  
Yiman Zhao ◽  
Yajing Chen ◽  
Zhichao Xiong ◽  
Xudong Sun ◽  
Quanqing Zhang ◽  
...  
2018 ◽  
Vol 41 (9) ◽  
pp. NA-NA
Author(s):  
Linlin Chen ◽  
Di Ding ◽  
Qianying Sheng ◽  
Long Yu ◽  
Xiuping Liu ◽  
...  

2018 ◽  
Vol 41 (9) ◽  
pp. 2003-2011 ◽  
Author(s):  
Linlin Chen ◽  
Di Ding ◽  
Qianying Sheng ◽  
Long Yu ◽  
Xiuping Liu ◽  
...  

2019 ◽  
Vol 26 (2) ◽  
pp. 63-71
Author(s):  
Ling Leng ◽  
Ying Wang ◽  
Peixian Yang ◽  
Takashi Narihiro ◽  
Masaru Konishi Nobu ◽  
...  

Chain elongation of volatile fatty acids for medium chain fatty acids production (e.g. caproate) is an attractive approach to treat wastewater anaerobically and recover resource simultaneously. Undefined microbial consortia can be tailored to achieve chain elongation process with selective enrichment from anaerobic digestion sludge, which has advantages over pure culture approach for cost-efficient application. Whilst the metabolic pathway of the dominant caproate producer, Clostridium kluyveri, has been annotated, the role of other coexisting abundant microbiomes remained unclear. To this end, an ethanol-acetate fermentation inoculated with fresh digestion sludge at optimal conditions was conducted. Also, physiological study, thermodynamics and 16 S rRNA gene sequencing to elucidate the biological process by linking the system performance and dominant microbiomes were integrated. Results revealed a possible synergistic network in which C. kluyveri and three co-dominant species, Desulfovibrio vulgaris, Fusobacterium varium and Acetoanaerobium sticklandii coexisted. D. vulgaris and A. sticklandii (F. varium) were likely to boost the carboxylates chain elongation by stimulating ethanol oxidation and butyrate production through a syntrophic partnership with hydrogen (H2) serving as an electron messenger. This study unveils a synergistic microbial network to boost caproate production in mixed culture carboxylates chain elongation.


2017 ◽  
Vol 35 (7) ◽  
pp. 688
Author(s):  
Hongwei WANG ◽  
Zhongshan LIU ◽  
Xiaojun PENG ◽  
Junjie OU ◽  
Mingliang YE

1995 ◽  
Vol 31 (2) ◽  
pp. 235-243 ◽  
Author(s):  
Imre Takács ◽  
Ernö Fleit

Two common causes of filamentous bulking of activated sludge are low dissolved oxygen (DO) concentration and low food to microorganism (F/M) ratio in the activated sludge system. A dynamic mathematical model was developed to simulate the population dynamics of two groups of bacteria, floc-formers and filaments within the microenvironment of the activated sludge floc. An arbitrary grid of 50 by 50 elements was applied to a hypothetical floc of maximum 100 μm in diameter. The concentration of DO and soluble substrate was calculated inside the floc core under different bulk concentration conditions in order to simulate the effect of heterogeneous, gradient-governed microenvironments on dual species composition. Dynamic simulation runs were performed to calculate the growth of the two morphological types of microorganisms inside the floc under diffusion governed conditions. The results indicate that the method accurately predicts the onset of excessive filamentous growth (directly linked to bulking) even when traditional models neglecting diffusion limitation fail to do so. The positive feedback effect of the non-random (unidirectional) growth on the selective enrichment of filamentous organisms under electron acceptor (DO) or soluble substrate (F/M) limited conditions is demonstrated.


1995 ◽  
Vol 31 (5-6) ◽  
pp. 291-298
Author(s):  
Sally A. Anderson ◽  
Gillian D. Lewis ◽  
Michael N. Pearson

Specific gene probe detection methods that utilise a non-selective culturing step were tested for the ability to recognise the presence of quiescent enteric bacteria (Escherichia coli and Enterococcus faecalis ) within illuminated freshwater and seawater microcosms. An E. coli specific uidA gene probe and a 23S rRNA oligonucleotide probe for Enterococci were compared with recoveries using membrane filtration and incubation on selective media (mTEC and mE respectively). From these microcosm experiments a greater initial detection (from 4 hours to 1 day) of E. coli and Ent. faecalis using gene probe methods was observed. Additionally, a comparison of E. coli direct viable counts (DVC) in sunlight exposed microcosms with recoveries by selective media and gene probe methods revealed a large number of viable non-culturable cells. This suggests that enumeration of E. coli by a gene probe method is limited by the replication of the bacteria during the initial non-selective enrichment step. The detection of stressed Ent. faecalis by the oligonucleotide gene probe method was significantly greater than recovery on selective mE agar, indicating an Enterococci non-growth phase.


Sign in / Sign up

Export Citation Format

Share Document