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Recombinant HSP20 was made in BL21 bacteria from a human HSP20 clone (B53814) obtained from the EST collaboration.
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This phenotype was not evident in bacteria obtained from a human gastric biopsy, where all cells expressed high-molecular-weight O-antigen chains, which thus may be the preferred phenotype for H. pylori colonizing human gastric mucosa.
However, the MLST database of P. acnes only contains human isolates, which prevents determination as to whether the bacteria were from a human source.
B. cereus F65185 is a mesophilic bacterium sourced from a human wound containing one lantibiotic/lantipeptide cluster which is unusual in that 3 orfs separate the putative LanB and C genes and the two have a divergent orientation.
In this manner, we identified Wip4 and Wip5 from earthworm gut bacteria, Frp2 from a fern rhizosphere bacterium and Htp1 from a human tonsil bacterium.
Two of the three 5S ribosomal RNA sequences analyzed in that work were from purple bacteria, and the third was from a human cell line.
Bacteria from the human gut are equipped with an arsenal of carbohydrate-active enzymes that degrade dietary and host-derived glycans.
Their analysis uncovered a novel camouflage mechanism that may help hide the bacteria from the human immune system.
A similar circumstance has been found in another study of bacteria from the human intestine [ 7].
They focused on two enzymes: One, from a bacterium that causes infant meningitis, converted type A blood into type O, while another, from a human gut bacterium, converted type B to type O. (The two enzymes together convert type AB to type O).
Bacteria from the human gut show similar extensive repertoires of GH and GT genes [18], and it is apparent that this is a feature of bacteria from gastrointestinal environments.
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