In vivo imaging of Escherichia coli and Lactococcus lactis in murine intestines using a reporter luciferase gene

2012 ◽  
Vol 21 (3) ◽  
pp. 917-920 ◽  
Author(s):  
Mi-Sook Lee ◽  
Gi-Seong Moon
2008 ◽  
pp. 2331 ◽  
Author(s):  
W. Matthew Leevy ◽  
Timothy N. Lambert ◽  
James R. Johnson ◽  
Joshua Morris ◽  
Bradley D. Smith

2014 ◽  
Vol 1837 ◽  
pp. e83
Author(s):  
Sabrina Burschel ◽  
Heiko Erhardt ◽  
Conrad Mullineaux ◽  
Mark Leake ◽  
Thorsten Friedrich

The Analyst ◽  
2020 ◽  
Vol 145 (1) ◽  
pp. 177-183 ◽  
Author(s):  
Kunhao Qin ◽  
Dongfang Zhang ◽  
Yafang Ding ◽  
Xiaodan Zheng ◽  
Yingying Xiang ◽  
...  

The schematic of the synthesis route for fluorescent CDs-WT and the applications in the bioimaging and detection for p-NP is presented.


2008 ◽  
Vol 10 (6) ◽  
pp. 1249-1258 ◽  
Author(s):  
Sofie Notebaert ◽  
Harald Carlsen ◽  
Daniel Janssen ◽  
Peter Vandenabeele ◽  
Rune Blomhoff ◽  
...  

2009 ◽  
Vol 75 (19) ◽  
pp. 6306-6311 ◽  
Author(s):  
Shota Atsumi ◽  
Zhen Li ◽  
James C. Liao

ABSTRACTA pathway toward isobutanol production previously constructed inEscherichia coliinvolves 2-ketoacid decarboxylase (Kdc) fromLactococcus lactisthat decarboxylates 2-ketoisovalerate (KIV) to isobutyraldehyde. Here, we showed that a strain lacking Kdc is still capable of producing isobutanol. We found that acetolactate synthase fromBacillus subtilis(AlsS), which originally catalyzes the condensation of two molecules of pyruvate to form 2-acetolactate, is able to catalyze the decarboxylation of KIV like Kdc both in vivo and in vitro. Mutational studies revealed that the replacement of Q487 with amino acids with small side chains (Ala, Ser, and Gly) diminished only the decarboxylase activity but maintained the synthase activity.


2016 ◽  
Vol 1857 ◽  
pp. e85
Author(s):  
Sabrina Burschel ◽  
Heiko Erhardt ◽  
Conrad Mullineaux ◽  
Mark Leake ◽  
Thorsten Friedrich

Agriculture ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 186
Author(s):  
Emmanuel Okello ◽  
Kristof Moonens ◽  
Joseph Erume ◽  
Henri De Greve

Post-weaning diarrhea (PWD) and edema disease (ED), caused by enterotoxigenic and Shiga toxin producing Escherichia coli (ETEC and STEC) strains, are important diseases of newly weaned piglets worldwide. The objective of this study is to develop a passive immunization strategy to protect piglets against PWD and ED using recombinant Lactococcus lactis added to piglet diet at weaning. The Variable Heavy chain domains of Heavy chain antibodies (VHHs) or Nanobodies (Nbs), directed against the fimbrial adhesins FaeG (F4 fimbriae) and FedF (F18 fimbriae) of E. coli were cloned and expressed on the surface of L. lactis. In vitro, the recombinant L. lactis strains agglutinated and inhibited adhesion of cognate F4 or F18 fimbriae expressing E. coli to pig villous preparation. In vivo, the anti-F4 L. lactis protected weaned piglets against a challenge with an F4-positive ETEC strain. Piglets supplemented with oral anti-F4 L. lactis showed reduced fecal E. coli shedding. We concluded that the surface expressed Nanobodies on L. lactis neutralized the adhesins of targeted E. coli and abrogated gut colonization, the first step in disease pathogenesis. As a proof of concept, we demonstrated the potential of passive immunization with recombinant L. lactis as a viable alternative to antibiotic prophylaxis in preventing piglet-post-weaning diarrhea.


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