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    <title>NOPR Collection: &lt;b&gt;Pages 1-76&lt;/b&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33544</link>
    <description>&lt;b&gt;Pages 1-76&lt;/b&gt;</description>
    <pubDate>Sat, 17 Oct 2026 05:15:29 GMT</pubDate>
    <dc:date>2026-10-17T05:15:29Z</dc:date>
    <item>
      <title>&lt;span style="font-size:11.0pt;mso-bidi-font-size: 12.0pt;font-family:"Times New Roman","serif";mso-fareast-font-family:"Times New Roman"; mso-bidi-font-family:Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US; mso-bidi-language:HI" lang="EN-GB"&gt;Production of α-galactosidase from &lt;i style="mso-bidi-font-style: normal"&gt;Aspergillus foetidus&lt;/i&gt; MTCC 6322 by solid state fermentation and its application in soymilk hydrolysis&lt;/span&gt;</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/33577</link>
      <description>Title: &lt;span style="font-size:11.0pt;mso-bidi-font-size: 12.0pt;font-family:"Times New Roman","serif";mso-fareast-font-family:"Times New Roman"; mso-bidi-font-family:Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US; mso-bidi-language:HI" lang="EN-GB"&gt;Production of α-galactosidase from &lt;i style="mso-bidi-font-style: normal"&gt;Aspergillus foetidus&lt;/i&gt; MTCC 6322 by solid state fermentation and its application in soymilk hydrolysis&lt;/span&gt;
Authors: Boopathy, Naidu Ramachandra; Gupta, Rishikesh Kumar; Ramudu, Kamini Numbi
Abstract: &lt;span style="font-size:11.0pt;mso-bidi-font-size:&#xD;
12.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";="" mso-bidi-font-family:mangal;mso-ansi-language:en-gb;mso-fareast-language:en-us;="" mso-bidi-language:hi"="" lang="EN-GB"&gt;The production of α-galactosidase from the wild fungal&#xD;
strain &lt;i style="mso-bidi-font-style:normal"&gt;Aspergillus foetidus&lt;/i&gt; MTCC 6322&#xD;
using solid state fermentation (SSF), its characterization, and its efficacy in&#xD;
the hydrolysis of soymilk using response surface methodology were studied. The optimum conditions for production of α-galactosidase by SSF&#xD;
were: wheat bran (10 g), moisture content (64%), inoculum volume (1.0 mL; 6 ×&#xD;
10&lt;sup&gt;7&lt;/sup&gt; spores/mL) with a yield of 4.1 × 10&lt;sup&gt;3&lt;/sup&gt; units per gram&#xD;
dry substrate (U/gds) at 96 h. The enzyme showed optimum activity at pH 6.0,&#xD;
temperature 40°C, pH stability between 5.0-8.0, and temperature stability&#xD;
between 30-40°C. The enzyme was stable in the presence of trypsin, lipase, and&#xD;
collagenase and it showed susceptibility of the substrates such as raffinose,&#xD;
melibiose, guar gum and soymilk&lt;b&gt; &lt;/b&gt;to hydrolysis in varying degrees. The&#xD;
optimized conditions for soymilk hydrolysis were: soymilk (10 mL) from defatted&#xD;
soybean meal (1.5%), &#xD;
α-galactosidase (0.15 UmL&lt;sup&gt;-1&lt;/sup&gt;) at 30°C, pH 6.0 and duration of 1 h.&lt;/span&gt;
Page(s): 72-75</description>
      <pubDate>Fri, 01 Jan 2016 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/33577</guid>
      <dc:date>2016-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Purification and characterization of chitinase from &lt;i&gt;Streptomyces &lt;/i&gt;&lt;i style="mso-bidi-font-style:normal"&gt;violascens&lt;/i&gt; NRRL B2700</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/33576</link>
      <description>Title: Purification and characterization of chitinase from &lt;i&gt;Streptomyces &lt;/i&gt;&lt;i style="mso-bidi-font-style:normal"&gt;violascens&lt;/i&gt; NRRL B2700
Authors: Gangwar, Mamta; Singh, Vineeta; Pandey, Asheesh Kumar; Tripathi, CKM; Mishra, BN
Abstract: &lt;span style="font-size:11.0pt;font-family:&#xD;
" times="" new="" roman","serif";mso-fareast-font-family:timesnewroman;mso-bidi-font-family:="" mangal;mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:="" hi"="" lang="EN-GB"&gt;Chitinase is one of the important enzymes as it is directly linked to&#xD;
Chitin that has wide&lt;span style="font-size:11.0pt;font-family:&#xD;
" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";mso-bidi-font-family:="" mangal;mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:="" hi"="" lang="EN-GB"&gt; applications in industrial, medical and commercial fields for its&#xD;
biocompatibility and biodegradability. Here, we report &lt;span style="font-size:11.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:="" timesnewroman;mso-bidi-font-family:mangal;mso-ansi-language:en-gb;mso-fareast-language:="" en-us;mso-bidi-language:hi"="" lang="EN-GB"&gt;extracellular chitinase production by &lt;i&gt;Streptomyces&#xD;
&lt;/i&gt;&lt;i style="mso-bidi-font-style:normal"&gt;violascens &lt;/i&gt;NRRL B2700 under submerged&#xD;
fermentation condition. Chitinase production started after 10 h of incubation&#xD;
and reached to maximum level at 72 h of cultivation. Studies on the influence&#xD;
of additional carbon and nitrogen sources on chitinase production revealed that&#xD;
maltose, xylose, fructose, lactose, soybean meal and ammonium nitrate served as&#xD;
good carbon and nitrogen sources to enhance chitinase yield by 1.6 to 6 fold.&#xD;
Medium supplemented with 1% colloidal chitin produced high chitinase&#xD;
concentration (0.1714 U/mg). The enzyme &lt;span style="font-size:11.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:="" "times="" roman";mso-bidi-font-family:mangal;mso-ansi-language:en-gb;="" mso-fareast-language:en-us;mso-bidi-language:hi;mso-bidi-font-weight:bold"="" lang="EN-GB"&gt;chitinase&#xD;
was purified from the culture broth by 75% ammonium sulphate precipitation,&#xD;
DEAE-cellulose ion-exchange and sephadex G-100 gel filtration. The molecular&#xD;
mass of the purified chitinase was 65 kDa as estimated by SDS-PAGE. The&#xD;
apparent &lt;span style="font-size:11.0pt;font-family:" times="" new="" roman","serif";="" mso-fareast-font-family:"times="" roman";mso-bidi-font-family:mangal;="" background:white;mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:="" hi"="" lang="EN-GB"&gt;Michaelis constant (&lt;span style="font-size:11.0pt;&#xD;
font-family:" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";="" mso-bidi-font-family:mangal;mso-ansi-language:en-gb;mso-fareast-language:en-us;="" mso-bidi-language:hi;mso-bidi-font-weight:bold"="" lang="EN-GB"&gt;K&lt;sub&gt;m&lt;/sub&gt;) and &lt;span style="font-size:11.0pt;font-family:" times="" new="" roman","serif";="" mso-fareast-font-family:"times="" roman";mso-bidi-font-family:mangal;="" background:white;mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:="" hi"="" lang="EN-GB"&gt;the maximum rate &lt;span style="font-size:11.0pt;&#xD;
font-family:" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";="" mso-bidi-font-family:mangal;mso-ansi-language:en-gb;mso-fareast-language:en-us;="" mso-bidi-language:hi;mso-bidi-font-weight:bold"="" lang="EN-GB"&gt;(V&lt;sub&gt;max&lt;/sub&gt;)&lt;sub&gt; &lt;/sub&gt;of&#xD;
the enzyme for colloidal chitin were 1.556 mg/mL and 2.680 µM/min/mg,&#xD;
respectively suggested high affinity towards chitin. Possibly, it is the first&#xD;
report on production of chitinase from &lt;i&gt;S&lt;/i&gt;&lt;span style="mso-bidi-font-style:&#xD;
italic"&gt;.&lt;i&gt; &lt;/i&gt;&lt;i style="mso-bidi-font-style:normal"&gt;&lt;span style="font-size:11.0pt;font-family:" times="" new="" roman","serif";="" mso-fareast-font-family:"times="" roman";mso-bidi-font-family:mangal;="" mso-ansi-language:en-us;mso-fareast-language:zh-cn;mso-bidi-language:hi;="" mso-bidi-font-weight:bold"="" lang="EN-US"&gt;violascens&lt;/span&gt;&lt;/i&gt;&lt;span style="font-size:11.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:="" "times="" roman";mso-bidi-font-family:mangal;mso-ansi-language:en-us;="" mso-fareast-language:zh-cn;mso-bidi-language:hi;mso-bidi-font-weight:bold"="" lang="EN-US"&gt;&#xD;
NRRL B2700. The findings were encouraging, especially for cost effective&#xD;
production, and further warrants media and purification optimization studies&#xD;
for enhanced yield.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 64-71</description>
      <pubDate>Fri, 01 Jan 2016 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/33576</guid>
      <dc:date>2016-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Effect of sweetener and flavoring agent on oxidative indices,  liver and kidney function levels in rats</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/33575</link>
      <description>Title: Effect of sweetener and flavoring agent on oxidative indices,  liver and kidney function levels in rats
Authors: Amin, Kamal A; Al-muzafar, Hessa M; Elsttar, Adel H Abd
Abstract: &lt;span style="font-size:11.0pt;mso-bidi-font-size:&#xD;
9.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-US"&gt;Food&#xD;
additives while attract consumers, improve quality, control weight and replace&#xD;
sugar, may affect seriously children and adults health. Here, we investigated&#xD;
the adverse effects of saccharin and methylsalicyltaes&#xD;
as sweetener and flavoring agent on lipid profile, blood glucose,&lt;span dir="RTL" style="font-size:9.0pt;mso-ansi-font-size:&#xD;
11.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-US"&gt; &lt;span style="font-size:11.0pt;mso-bidi-font-size:&#xD;
9.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-US"&gt;renal,&#xD;
hepatic function and oxidative stress/antioxidants (lipid peroxidation,&#xD;
catalase and reduced glutathione in liver tissues). Saccharin and&#xD;
methylsalicylate were administered orally in young male albino rats at low and&#xD;
high dose for 30 days. Rats were divided into 5 groups, 1&lt;sup&gt;st&lt;/sup&gt; control&#xD;
group, 2&lt;sup&gt;nd&lt;/sup&gt; and 3&lt;sup&gt;rd&lt;/sup&gt; (low and high saccharin-treated&#xD;
groups) and 4&lt;sup&gt;th&lt;/sup&gt; and 5&lt;sup&gt;th&lt;/sup&gt; (low and high&#xD;
methylsalicylate-treated group). Serum total cholesterol, triglyceride, glucose&#xD;
levels and body weight gain were found decreased in saccharin high dose group compared&#xD;
to control.&lt;span style="font-size:11.0pt;mso-bidi-font-size:&#xD;
9.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-eg"="" lang="EN-US"&gt; &lt;span style="font-size:11.0pt;mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"="" lang="EN-US"&gt;Rats consumed high dose &lt;span style="font-size:11.0pt;mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-eg"="" lang="EN-US"&gt;of&lt;span style="font-size:11.0pt;&#xD;
mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:="" "times="" roman";mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-US"&gt; saccharin showed a significant decrease in serum&#xD;
triglycerides, cholesterol and LDL levels.&lt;span style="font-size:11.0pt;mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-eg"="" lang="EN-US"&gt; Low and high doses of saccharin exhibited a&#xD;
significant increase in liver function marker of ALT, AST, ALP activity, total&#xD;
proteins and albumin levels and &lt;span style="font-size:11.0pt;&#xD;
mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:="" "times="" roman";mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-US"&gt;renal function test (urea and creatinine levels)&lt;span style="font-size:11.0pt;mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-eg"="" lang="EN-US"&gt; in comparison with control group. &lt;span style="font-size:11.0pt;mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"="" lang="EN-US"&gt;Further, saccharin at high dose induced&#xD;
significant decrease in liver GSH levels, catalase and SOD activity and&#xD;
increase in hepatic MDA level. &lt;span style="font-size:11.0pt;&#xD;
mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:="" "times="" roman";mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-eg"="" lang="EN-US"&gt;Overall&lt;span style="font-size:11.0pt;&#xD;
mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:="" "times="" roman";mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-US"&gt; saccharin harmfully altered biochemical markers in&#xD;
liver and kidney at higher as well as lower doses. Whereas,&lt;span style="font-size:11.0pt;mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-eg"="" lang="EN-US"&gt; &lt;span style="font-size:11.0pt;&#xD;
mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:="" "times="" roman";mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-US"&gt;methyl salicylates did not pose a risk for renal&#xD;
function and hepatic oxidative markers.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 56-63</description>
      <pubDate>Fri, 01 Jan 2016 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/33575</guid>
      <dc:date>2016-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Protective role of diet supplements Spirulina and Tamarind fruit pulp on  kidney in sodium fluoride exposed Swiss albino mice: Histological and biochemical indices</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/33574</link>
      <description>Title: Protective role of diet supplements Spirulina and Tamarind fruit pulp on  kidney in sodium fluoride exposed Swiss albino mice: Histological and biochemical indices
Authors: Yadav, N; Sharma, Shweta; Sharma, KP; Pandey, A; Pareek, P; Sharma, Subhasini
Abstract: &lt;span style="font-size:11.0pt;font-family:&#xD;
" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";mso-bidi-font-family:="" mangal;mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:="" hi"="" lang="EN-GB"&gt;Fluoride toxicity through potable water, particularly ground water, is not&#xD;
uncommon in countries such as India, China, Iran, Iraq, Turkey, parts of Africa&#xD;
and Afghanistan. Kidney being the main organ involved in fluoride removal, it&#xD;
accumulates considerable amount of fluoride. Here, we report toxic effects of&#xD;
oral exposure of Swiss albino mice to fluoride (sub-acute: 190 mg/kg body wt.&#xD;
for 7days; and sub-chronic: 94 mg/kg body wt. for 90 days) and recovery of&#xD;
sub-chronic fluoride exposed mice after 90 days of sodium fluoride (NaF)&#xD;
withdrawal. The role of diet supplements (Spirulina and tamarind fruit pulp @&#xD;
230 mg/kg body wt. independently as well as in combination) in amelioration of&#xD;
fluoride toxicity has also been screened. Compared with controls, feed intake&#xD;
decreased from 3-43%, body wt. 4-18%, and kidney wt. 5-12% in treated mice&#xD;
(except diet supplement groups of sub-chronic exposure) while their water&#xD;
intake increased from 4-43%. Histopathological changes in the cortical region&#xD;
of kidney in fluoride treated mice were as&#xD;
follows: dilation of bowman’s capsule and thickening of its parietal and&#xD;
visceral layer; alterations in glomeruli size and their sclerotization;&#xD;
increase in bowman’s space; proliferation of mesangial cells; reduction in&#xD;
podocyte counts; and dilation of proximal and distal tubules. Fluoride exposure&#xD;
altered tissue biochemistry (protein, acid phosphatase and alkaline phosphatase&#xD;
content) and increased urea (23-58%) and creatinine content (14-127%) in the&#xD;
serum. Sub-acute exposure was found more toxic. The diet modulation not only&#xD;
reduced fluoride toxicity but also led to better recovery of treated mice after&#xD;
withdrawal, especially in combination.&lt;/span&gt;
Page(s): 44-55</description>
      <pubDate>Fri, 01 Jan 2016 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/33574</guid>
      <dc:date>2016-01-01T00:00:00Z</dc:date>
    </item>
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