<p>The whole cell lysate (W) and soluble fraction (S) of <i>B. subtilis</i> DB104-pRPA-NAP, HP-NAP-containing flow-through fractions (F) obtained by DEAE Sephadex chromatography, and the concentrated HP-NAP (C) from flow-through fractions were analyzed by SDS-PAGE (<b>A</b>), native-PAGE (<b>B</b>), and immunoblotting (<b>C</b>) with an anti-HP-NAP antibody (MAb 16F4). Molecular weights (M) in kDa are indicated on the left of stained gels and the blot.</p
<p>(A) Expression of HcpA by transformed <i>B. burgdorferi</i> B313 was assessed using immunoblot an...
<p>(A) Gly-pro-AMC zymogram of supernatants from <i>P. pastoris</i> transformed with empty vector an...
<p>(A), insoluble and soluble fractions of BPSM (wt control; lanes 1 and 4), BPRM1 (deletion mutant;...
<p><i>B. subtilis</i> DB104-pRPA-NAP and <i>B. subtilis</i> DB104 were incubated at 37°C for 15 hr. ...
<p>A, The soluble fraction from the whole cell lysate of <i>B. subtilis</i> DB104-pRPA-NAP was appli...
<p>Purified HP-NAP and protein molecular weight makers were subjected to gel-filtration chromatograp...
<p>The soluble fraction from the whole cell lysate of <i>B. subtilis</i> DB104-pRPA-NAP was adjusted...
a<p>From 0.84 g of <i>B. subtilis</i> cell paste obtained from 300 ml of bacterial culture.</p>b<p>P...
Helicobacter pylori neutrophil-activating protein (HP-NAP), a major virulence factor of Helicobacter...
[[abstract]]Helicobacter pylori neutrophil-activating protein (HP-NAP), a major virulence factor of ...
<p>HP-NAP purified by gel-filtration chromatography at pH 9.0 (25°C) was kept at pH 9.0 or adjusted ...
<div><p><i>Helicobacter pylori</i> neutrophil-activating protein (HP-NAP), a major virulence factor ...
<p>(A) Identification of opPPL expressed in <i>P.pastoris</i> by 12% SDS-PAGE. Lane M, molecular mar...
<p>Supernatant samples from induced <i>Pp</i>CV1 cells were analyzed by (A) silver staining of SDS-P...
<p>(A) SDS-PAGE of recombinant BjATl purified on Ni-NTA resin column. Lane 1, molecular mass standar...
<p>(A) Expression of HcpA by transformed <i>B. burgdorferi</i> B313 was assessed using immunoblot an...
<p>(A) Gly-pro-AMC zymogram of supernatants from <i>P. pastoris</i> transformed with empty vector an...
<p>(A), insoluble and soluble fractions of BPSM (wt control; lanes 1 and 4), BPRM1 (deletion mutant;...
<p><i>B. subtilis</i> DB104-pRPA-NAP and <i>B. subtilis</i> DB104 were incubated at 37°C for 15 hr. ...
<p>A, The soluble fraction from the whole cell lysate of <i>B. subtilis</i> DB104-pRPA-NAP was appli...
<p>Purified HP-NAP and protein molecular weight makers were subjected to gel-filtration chromatograp...
<p>The soluble fraction from the whole cell lysate of <i>B. subtilis</i> DB104-pRPA-NAP was adjusted...
a<p>From 0.84 g of <i>B. subtilis</i> cell paste obtained from 300 ml of bacterial culture.</p>b<p>P...
Helicobacter pylori neutrophil-activating protein (HP-NAP), a major virulence factor of Helicobacter...
[[abstract]]Helicobacter pylori neutrophil-activating protein (HP-NAP), a major virulence factor of ...
<p>HP-NAP purified by gel-filtration chromatography at pH 9.0 (25°C) was kept at pH 9.0 or adjusted ...
<div><p><i>Helicobacter pylori</i> neutrophil-activating protein (HP-NAP), a major virulence factor ...
<p>(A) Identification of opPPL expressed in <i>P.pastoris</i> by 12% SDS-PAGE. Lane M, molecular mar...
<p>Supernatant samples from induced <i>Pp</i>CV1 cells were analyzed by (A) silver staining of SDS-P...
<p>(A) SDS-PAGE of recombinant BjATl purified on Ni-NTA resin column. Lane 1, molecular mass standar...
<p>(A) Expression of HcpA by transformed <i>B. burgdorferi</i> B313 was assessed using immunoblot an...
<p>(A) Gly-pro-AMC zymogram of supernatants from <i>P. pastoris</i> transformed with empty vector an...
<p>(A), insoluble and soluble fractions of BPSM (wt control; lanes 1 and 4), BPRM1 (deletion mutant;...