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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10642" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/10642</id>
  <updated>2026-10-09T18:36:06Z</updated>
  <dc:date>2026-10-09T18:36:06Z</dc:date>
  <entry>
    <title>Simultaneous removal of NO&lt;sub&gt;X&lt;/sub&gt; and SO&lt;sub&gt;2&lt;/sub&gt; in exhausted gas through landfill leachate</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10655" />
    <author>
      <name>Han, Yaqiong</name>
    </author>
    <author>
      <name>Zhang, Weijiang</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10655</id>
    <updated>2010-11-21T16:30:32Z</updated>
    <published>2010-12-01T00:00:00Z</published>
    <summary type="text">Title: Simultaneous removal of NO&lt;sub&gt;X&lt;/sub&gt; and SO&lt;sub&gt;2&lt;/sub&gt; in exhausted gas through landfill leachate
Authors: Han, Yaqiong; Zhang, Weijiang
Abstract: Simultaneous&#xD;
removal of NOx and SO&lt;sub&gt;2&lt;/sub&gt; from exhausted gas were&#xD;
investigated by studying co-culture of sulfate reducing bacteria and anaerobic&#xD;
denitrifying bacteria, separated from landfill leachate. When H&lt;sub&gt;2&lt;/sub&gt;S, generated&#xD;
by sulfate reducing bacteria was chosen as the sole electron donor for anaerobic&#xD;
denitrifying bacteria, the co-culture system demonstrated a faster NO removal&#xD;
rate, higher stability and better permanence. When the feed gas flow rates of N&lt;sub&gt;2&lt;/sub&gt;&#xD;
and SO&lt;sub&gt;2&lt;/sub&gt; were maintained constant at 0.1 m&lt;sup&gt;3&lt;/sup&gt;/h and 16 ml/min respectively, the maximum&#xD;
NO-removal rate could be achieved at over 92% with NO feed gas kept between 2-6&#xD;
ml/min, while the SO&lt;sub&gt;2&lt;/sub&gt; removal rate was always above 95%. Long-term continuous&#xD;
removal of NO exhibited an evident periodicity of five days, however, the fluctuation&#xD;
range of NO-removal was decreasing. Moreover, the decrease of the gas flow rate&#xD;
and the increase in NO&#xD;
inlet concentration could contribute to a higher NO-removal rate
Page(s): 1237-1242</summary>
    <dc:date>2010-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Biological activity of sea anemone proteins: II. Cytolysis and cell line toxicity</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10654" />
    <author>
      <name>Ravindran, Vinoth S</name>
    </author>
    <author>
      <name>Kannan, L</name>
    </author>
    <author>
      <name>Venkateshvaran, K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10654</id>
    <updated>2010-11-20T16:30:24Z</updated>
    <published>2010-12-01T00:00:00Z</published>
    <summary type="text">Title: Biological activity of sea anemone proteins: II. Cytolysis and cell line toxicity
Authors: Ravindran, Vinoth S; Kannan, L; Venkateshvaran, K
Abstract: Potent cytolytic activity was exhibited by&#xD;
proteins extracted from three sea anemones viz.&lt;i&gt; Heteractis magnifica&lt;/i&gt;,&lt;b&gt; &lt;/b&gt;&lt;i&gt;Stichodactyla haddoni&lt;/i&gt; and&lt;i&gt;&#xD;
Paracodylactis sinensis&lt;/i&gt; by affecting the red blood corpuscles (RBC) and the&#xD;
mouse fibroblast cell line (L929) and leukemia cell line (P388). Crude toxin of&#xD;
all the three anemone species induced spontaneous hemolysis of chicken, goat&#xD;
and human erythrocytes. The crude toxin of &lt;i style=""&gt;H.&#xD;
magnifica&lt;/i&gt; (0.98 mg/ml) elicited hemolysis at levels of 4096, 512 and 4096&#xD;
HU (hemolytic unit) in chicken, goat and human erythrocytes respectively.&#xD;
Subsequently, the crude toxin of &lt;i style=""&gt;S.haddoni&lt;/i&gt;&#xD;
(0.82 mg/ml) exhibited a hemolytic activity of 256, 128 and 512 HU and that of &lt;i style=""&gt;P. sinensis&lt;/i&gt; (0.60 mg/ml) had a hemolytic activity of 128, 4096 and 512 HU.&#xD;
Most of the partially purified proteins of these anemones also exhibited the&#xD;
activity against the three different erythrocytes. The viability of L929 and&#xD;
P388 was adversely affected on adding the crude toxins. The symptoms of&#xD;
toxicity shown by the cells were rounding, lysis and detachment from the&#xD;
substratum. These effects were the least in &lt;i&gt;S&lt;/i&gt;&lt;i style=""&gt;. haddoni,&lt;/i&gt; as compared to those the crude toxins of the other two&#xD;
species. Inhibition of growth of L929 exhibited by the toxin of the three&#xD;
species ranged between 61.08 and 93.38%. Similarly, inhibition of the growth of&#xD;
P388 ranged between 51.32 and 86.16%&lt;i style=""&gt;. &lt;/i&gt;The&#xD;
present investigation reveal the cytotoxic nature of anemone toxins.
Page(s): 1233-1236</summary>
    <dc:date>2010-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Biological activity of sea anemone proteins: I. Toxicity and histopathology</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10653" />
    <author>
      <name>Ravindran, Vinoth S</name>
    </author>
    <author>
      <name>Kannan, L</name>
    </author>
    <author>
      <name>Venkateshvaran, K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10653</id>
    <updated>2010-11-19T16:30:35Z</updated>
    <published>2010-12-01T00:00:00Z</published>
    <summary type="text">Title: Biological activity of sea anemone proteins: I. Toxicity and histopathology
Authors: Ravindran, Vinoth S; Kannan, L; Venkateshvaran, K
Abstract: The crude as well as partially purified protein fractions from anemone&#xD;
species viz.&lt;i&gt; Heteractis magnifica, Stichodactyla haddoni &lt;/i&gt;and&lt;i&gt; Paracodylactis&#xD;
sinensis&lt;/i&gt;, collected from the Gulf of Mannar,&#xD;
south east coast of India&#xD;
were found to be toxic at different levels to mice. The mice showed behavioral&#xD;
changes such as loss of balance, opaque eyes, tonic convulsions, paralysis,&#xD;
micturiction, flexing of muscles, prodding (insensitive to stimulii), foaming&#xD;
from mouth and exophthalmia. The toxic proteins upon envenomation produced&#xD;
several chronic and lethal histopathological changes like formation of pycnotic&#xD;
nuclii and glial nodules in the brain; heamolysis, thrombosis and myocardial&#xD;
haemorrhage in the heart; granulomatous lesions, and damage to the hepatic&#xD;
cells in the liver and haemorrhage throughout the kidney parenchyma and&#xD;
shrinkage of glomerular tufts in the kidney. The toxins proved to be neurotoxic,&#xD;
cardiotoxic, nephrotoxic and hepatotoxic by their action on internal organ&#xD;
systems. The toxins were also thermostable till 60&lt;sup&gt;o&lt;/sup&gt;C and had&#xD;
considerable shelf life.
Page(s): 1225-1232</summary>
    <dc:date>2010-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Screening of certain medicinal plants from India for their anti-quorum sensing activity</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10652" />
    <author>
      <name>Zahin, Maryam</name>
    </author>
    <author>
      <name>Hasan, Sameena</name>
    </author>
    <author>
      <name>Aqil, Farrukh</name>
    </author>
    <author>
      <name>Khan, Mohd. Sajjad Ahmad</name>
    </author>
    <author>
      <name>Husain, Fohad Mabood</name>
    </author>
    <author>
      <name>Ahmad, Iqbal</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10652</id>
    <updated>2010-11-22T16:30:19Z</updated>
    <published>2010-12-01T00:00:00Z</published>
    <summary type="text">Title: Screening of certain medicinal plants from India for their anti-quorum sensing activity
Authors: Zahin, Maryam; Hasan, Sameena; Aqil, Farrukh; Khan, Mohd. Sajjad Ahmad; Husain, Fohad Mabood; Ahmad, Iqbal
Abstract: Discovery of quorum sensing (QS) system to&#xD;
coordinate virulence and biofilm formation in bacterial pathogens has triggered&#xD;
search for safe, stable and non-toxic anti-QS compounds from natural products.&lt;b style=""&gt; &lt;/b&gt;Ethanolic extracts of 24 Indian&#xD;
medicinal plants were tested by agar well and disc diffusion assay for anti-QS&#xD;
activity using &lt;i style=""&gt;Chromobacterium violaceum &lt;/i&gt;(CV12472&#xD;
and CVO26) reporter strains. AHL from &lt;i style=""&gt;C.&#xD;
violaceum &lt;/i&gt;CV31532 was isolated and partially purified for its use in CVO26&#xD;
based bioassay. Effect on swarming-motility of &lt;i style=""&gt;Pseudomonas aeruginosa &lt;/i&gt;(PAO1) was also recorded at sub-MIC&#xD;
concentrations of extracts. Of the 24 medicinal plants screened &lt;i style=""&gt;Hemidesmus indicus &lt;/i&gt;(L.) Schult (root), &lt;i style=""&gt;Holarrhena antidysenterica&lt;/i&gt; (Roth)A.DC.&#xD;
(bark),&lt;i style=""&gt; Mangifera indica &lt;/i&gt;L.&lt;i style=""&gt; &lt;/i&gt;(seed)&lt;i style=""&gt; Punica granatum &lt;/i&gt;L. (pericarp) and &lt;i style=""&gt;Psoralea corylifolia &lt;/i&gt;L&lt;i style=""&gt;. &lt;/i&gt;(seed) demonstrated varying level of inhibition of&#xD;
violacein production in the reporter strains. Moreover, a significant reduction&#xD;
in swarms was recorded over control. The inhibition of violacein production and&#xD;
swarming motility may be due to direct or indirect interference on QS by active&#xD;
constituents or the interactive effect of different phytocompounds present in&#xD;
the extracts. These plant extracts may be selected for activity guided&#xD;
fractionation to identify and characterize the active principle
Page(s): 1219-1224</summary>
    <dc:date>2010-12-01T00:00:00Z</dc:date>
  </entry>
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