Production of Poly(3-Hydroxybutyrate) by Recombinant Bacteria

Author(s):  
Sang Yup Lee ◽  
Jong-il Choi ◽  
Fulai Wang
Keyword(s):  
1997 ◽  
Vol 36 (10) ◽  
pp. 1-8 ◽  
Author(s):  
James D. Bryers ◽  
Robert R. Sharp

Exposure of plasmid recombinant microorganisms to an open environment, either inadvertently or intentionally, requires research into those fundamental processes that govern plasmid retention, transfer and expression. In the open environment, a majority of the microbial activity occurs associated with an interface, within thin biological layers consisting of cells and their insoluble extracellular polymer, layers known as biofilms. Current toxic wastewater or wastegas treatment reactors exploit bacterial biofilm systems for certain system operating advantages. Using recombinant bacteria within a biofilm reactor to degrade xenobiotic wastes requires finding a suitable host to harbor and express the desired plasmid phenotype. Suitable host characteristics include: the ability to produce copious amounts of biofilm, resistance to waste-related injury and toxicity, and the ability to retain and express the desired plasmid during long term operation. This paper reports on a laboratory evaluation of factors governing plasmid retention and the expression of trichloroethene (TCE) degradative capacity in both suspended and biofilm cultures.


1989 ◽  
Vol 264 (6) ◽  
pp. 3470-3477
Author(s):  
J P MacManus ◽  
C M L Hutnik ◽  
B D Sykes ◽  
A G Szabo ◽  
T C Williams ◽  
...  

2013 ◽  
Vol 8 (1) ◽  
pp. 22 ◽  
Author(s):  
Ima Avalos Vizcarra ◽  
Philippe Emge ◽  
Philipp Miermeister ◽  
Mamta Chabria ◽  
Rupert Konradi ◽  
...  

2000 ◽  
Vol 84-86 (1-9) ◽  
pp. 141-152 ◽  
Author(s):  
Joy Bethune Doran ◽  
Jennifer Cripe ◽  
Misty Sutton ◽  
Brian Foster

Author(s):  
Yangzhen Shu ◽  
Shanshan Li ◽  
Jingxi Xie ◽  
Kexin Guo ◽  
Conghui Cheng ◽  
...  

2000 ◽  
Vol 182 (23) ◽  
pp. 6857-6861 ◽  
Author(s):  
Beatriz Martı́nez ◽  
Jouko Sillanpää ◽  
Egbert Smit ◽  
Timo K. Korhonen ◽  
Peter H. Pouwels

The cbsA gene encoding the collagen-binding S-layer protein of Lactobacillus crispatus JCM5810 was expressed inL. casei ATCC 393T. The S-protein was not retained on the surface of the recombinant bacteria but was secreted into the medium. By translational fusion of CbsA to the cell wall sorting signal of the proteinase, PrtP, of L. casei, CbsA was presented at the surface, rendering the transformants able to bind to immobilized collagens.


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