scholarly journals Development of new enzymes and microbial cells for the enhancement of livestock feeds based on sugarcane fibre

Author(s):  
Tuan Tu Dam
BIOCELL ◽  
2018 ◽  
Vol 42 (3) ◽  
pp. 93-97 ◽  
Author(s):  
Mahmoud MOUSTAFA ◽  
Saad ALAMRI ◽  
Mohamed ELNOUBY ◽  
Tarek TAHA ◽  
M. A. ABU-SAIED ◽  
...  

BIO-PROTOCOL ◽  
2014 ◽  
Vol 4 (12) ◽  
Author(s):  
Marco Fischer ◽  
Dörte Falke ◽  
R. Sawers

2016 ◽  
Vol 228 ◽  
pp. 1-9 ◽  
Author(s):  
Oylum Erkus ◽  
Victor C.L. de Jager ◽  
Renske T.C.M. Geene ◽  
Ingrid van Alen-Boerrigter ◽  
Lucie Hazelwood ◽  
...  

2017 ◽  
Vol 3 (5) ◽  
pp. e1601984 ◽  
Author(s):  
Wen Wang ◽  
Lining Yao ◽  
Chin-Yi Cheng ◽  
Teng Zhang ◽  
Hiroshi Atsumi ◽  
...  
Keyword(s):  

2012 ◽  
Vol 40 (6) ◽  
pp. 1330-1335 ◽  
Author(s):  
Kamrul Hasan ◽  
Sunil A. Patil ◽  
Dónal Leech ◽  
Cecilia Hägerhäll ◽  
Lo Gorton

Electrochemical communication between micro-organisms and electrodes is the integral and fundamental part of BESs (bioelectrochemical systems). The immobilization of bacterial cells on the electrode and ensuring efficient electron transfer to the electrode via a mediator are decisive features of mediated electrochemical biosensors. Notably, mediator-based systems are essential to extract electrons from the non-exoelectrogens, a major group of microbes in Nature. The advantage of using polymeric mediators over diffusible mediators led to the design of osmium redox polymers. Their successful use in enzyme-based biosensors and BFCs (biofuel cells) paved the way for exploring their use in microbial BESs. The present mini-review focuses on osmium-bound redox systems used to date in microbial BESs and their role in shuttling electrons from viable microbial cells to electrodes.


1979 ◽  
Vol 57 (9) ◽  
pp. 1000-1007 ◽  
Author(s):  
George C. Carroll

Distribution patterns and total cell-volume estimates for needle microepiphytes are presented for three strata in the canopy of a single old-growth Douglas fir tree. Microbial cell volume was estimated by photographing transverse sections of needles, tracing microbial profiles on Mylar film, cutting out the tracings, and determining the pooled trace weights from various zones of each needle section. Microbial cells are concentrated in the midrib groove and over the stomatal zones of individual needles. Microbial cell volume on the upper needle surfaces increases during the 1st year and declines in subsequent years. Cell volumes on the lower needle surfaces increase from the 1st to the 3rd year and decrease from the 3rd to the 4th year. An increase in microbial cell volume occurs on both upper and lower surfaces from year 7 to year 8. Total microbial cell volume in relation to available needle surface area is greatest in the lower canopy and decreases with increasing height in the canopy. The total volume of microbial cells on needles was estimated to be 1093 cm3 for the entire tree.


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