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<title>05. Department of Microbiology</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/257" rel="alternate"/>
<subtitle/>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/257</id>
<updated>2026-05-10T15:06:22Z</updated>
<dc:date>2026-05-10T15:06:22Z</dc:date>
<entry>
<title>Purification of β-ketothiolase from halophilic archaea haloarcula sp.1 isolated from Bhavnagar coast,  Gujarat, India.</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/917" rel="alternate"/>
<author>
<name>Patadia, Apexa</name>
</author>
<author>
<name>Dave, Bharti P</name>
</author>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/917</id>
<updated>2023-05-10T07:19:05Z</updated>
<published>2016-07-01T00:00:00Z</published>
<summary type="text">Purification of β-ketothiolase from halophilic archaea haloarcula sp.1 isolated from Bhavnagar coast,  Gujarat, India.
Patadia, Apexa; Dave, Bharti P
Members of the Archaeal family have been determined to accumulate Poly (3-hydroxybutyrate) (PHB) during &#13;
their growth. A total of 13 extremely Halophilic Archaeal isolates designated as NPW-1 to NPW-13 were &#13;
capable of accumulating large amounts of PHB. Out of which best four isolates were selected from enzyme &#13;
assay. Since measurements of enzyme activities related to Archaeal PHB biosynthesis have never been &#13;
achieved, we investigated the first enzyme of PHB biosynthesis in Haloarcula sp.1 i.e., β-ketothiolase. Crude &#13;
extracts of strain cultivated under accumulating conditions showed maximum β-ketothiolase activity. β ketothiolase was partially purified by ammonium sulfate fractionation and highest activity was obtained in 60% &#13;
saturation fraction. This is the first description of an archaebacterial β-ketothiolase . Silver staining of the &#13;
purified enzyme (fraction 8) with SDS – PAGE showed that enzyme subunited molecular weight putatively &#13;
identified was 45 kDa.
</summary>
<dc:date>2016-07-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Isolation, screening and quantification  of Poly-β-hydroxybutyrate (PHB) from  extreme halophilic Archaea</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/916" rel="alternate"/>
<author>
<name>Patadia, Apexa</name>
</author>
<author>
<name>Dave, Bharti P</name>
</author>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/916</id>
<updated>2023-05-10T07:12:04Z</updated>
<published>2016-02-01T00:00:00Z</published>
<summary type="text">Isolation, screening and quantification  of Poly-β-hydroxybutyrate (PHB) from  extreme halophilic Archaea
Patadia, Apexa; Dave, Bharti P
The Archaea remain the most enigmatic of life’s three domains and halophiles constitute a very heterogeneous &#13;
group of extremophiles in this domain. Due to their special characteristics, they have been suggested to hold potential for a variety of biotechnological applications such as production of enzymes, compatible solutes, degradation of toxic compounds &#13;
and polymer production. The study aimed at efficient production and screening of thirteen haloarchael strains isolated from saltpans at &#13;
Newport and Nari for their ability to produce PHB. The production by these strains was determined by the spectrophotometric method and &#13;
results suggest that all the thirteen haloarchaeal isolates exhibited the ability to produce PHB, though to a varying extent. It was found that &#13;
PHB yield ranged from 0.01-1.17%. All the thirteen isolates were then subjected to secondary screening for examining DCW, PHB production &#13;
and yield as a function of incubation time. The maximum PHB production was by four haloarchaeal isolates viz., Haloarcula sp. 1 (3.77%), &#13;
Halorubrum sp. 2 (2.07%), Halobaculum sp. (2.02%) and Halobacterium salinarum (0.75%). The growth almost became constant after its &#13;
optimum period whereas, PHB yield declined.
</summary>
<dc:date>2016-02-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Prevalence of High-Risk Human Papilloma Virus (HR-HPV) as a risk  factor in HNSCC patients of Saurashtra region of Gujarat</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/914" rel="alternate"/>
<author>
<name>Parmar, Minaxi</name>
</author>
<author>
<name>Pandhi, Neepa</name>
</author>
<author>
<name>Patel, Prabhudas</name>
</author>
<author>
<name>Gupta, Vijaykumar</name>
</author>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/914</id>
<updated>2023-05-10T05:49:47Z</updated>
<published>2017-11-01T00:00:00Z</published>
<summary type="text">Prevalence of High-Risk Human Papilloma Virus (HR-HPV) as a risk  factor in HNSCC patients of Saurashtra region of Gujarat
Parmar, Minaxi; Pandhi, Neepa; Patel, Prabhudas; Gupta, Vijaykumar
Background: In India HNSCC comprises the largest group of malignancies with an incidence rate as &#13;
high as 30-40%.The present study was carried out to determine the prevalence of high-risk human &#13;
papilloma virus (HR-HPV) as a risk factor in HNSCC patients of Saurashtra region of Gujarat. &#13;
Method: Newly diagnosed 200 HNSCC patients were selected for the study. Sociodemographic and &#13;
clinical data were obtained through questionnaire. Detection of HPV-DNA was done from cancer &#13;
tissues by PCR amplification method using GP5+/GP6+ primers, E6 and E7 primers for HPV 16 and &#13;
HPV 18 genotypes. &#13;
Result: The prevalence of HPV high-risk (HR) types was 2% in HNSCC cancer cases. HPV 16 &#13;
genotype was identified while HPV 18 was absent in all the patients. The risk factor of HPV-HR &#13;
included younger age (&lt;55 years) and early age at first sexual intercourse. The other risk factors like &#13;
tobacco and alcohol were absent in these patients. The site of cancer was found to be base of tongue &#13;
and tonsil.&#13;
Conclusion: The specific characteristics found in HPV positive HNSCC cases are in accord with &#13;
distinctive characteristics of HPV positive HNSCC found worldwide. We can conclude that HR-HPV &#13;
infection may be responsible for HPV-positive HNSCC. However, the prevalence of HPV among &#13;
HNSCC is negligible which indicates that HPV is not an influential risk factor for oral cancer in this &#13;
region.
We gratefully acknowledge the funding &#13;
agency, the University Grant Commission &#13;
(UGC) of the Government of India, for &#13;
providing financial support in the form of minor &#13;
research project. We thank Head and Neck &#13;
cancer patients who participated in the study for &#13;
their co-operation. We are grateful to Dr. Geet &#13;
Gupta and Dr. Khyati Babaria from department &#13;
of pathology and Dr. Nirav Modi from &#13;
department of Head and Neck Surgery at Smt V.R. Desai Cancer Research centre, Rajkot and &#13;
their hospital staff for providing the HNSCC &#13;
tumor samples.
</summary>
<dc:date>2017-11-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Clinical evaluation of sialic acid in head and neck squamous cell carcinoma patients and tobacco chewers or smokers with no cancer</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/913" rel="alternate"/>
<author>
<name>Parmar, Minaxi</name>
</author>
<author>
<name>Pandhi, Neepa</name>
</author>
<author>
<name>Patel, Prabhudas</name>
</author>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/913</id>
<updated>2023-05-10T05:43:40Z</updated>
<published>2017-01-01T00:00:00Z</published>
<summary type="text">Clinical evaluation of sialic acid in head and neck squamous cell carcinoma patients and tobacco chewers or smokers with no cancer
Parmar, Minaxi; Pandhi, Neepa; Patel, Prabhudas
Sialic acid plays a significant role in cancer due to increased sialylation and sialyltransferase &#13;
activity. Patients with cancer have been reported to have significant elevations of serum Total Sialic &#13;
Acid (TSA) and Lipid Bound Sialic Acid (LBSA) levels as compared to control persons. The present &#13;
study was carried out to evaluate sialic acid levels in control, non-cancer smokers or tobacco &#13;
chewers and Head and Neck Squamous cell carcinoma (HNSCC) cancer patients. Blood samples &#13;
were obtained from the histopathologically diagnosed HNSCC patients, healthy controls and those &#13;
persons who were either smokers or tobacco chewers with no oral cancer. Serum TSA and LBSA &#13;
were measured spectrophotometrically. Serum TSA and LBSA levels were significantly elevated in &#13;
HNSCC patients compared to healthy control with P&lt;0.0001. These levels were also significantly &#13;
increased in individuals who were smokers or tobacco chewers with no cancer compared to healthy &#13;
control (P&lt;0.0001). Our results found significant elevation of serum sialic acid levels in HNSCC &#13;
patients and in smokers and tobacco chewers with no cancer as compared to control individuals. &#13;
These findings suggested role of tobacco in biochemical changes during the malignant transformation. &#13;
These results also indicate that these parameters can be utilized in diagnosis of the HNSCC.
I am grateful to Dr. Gupta VK, Medical &#13;
Director of Smt V. R. Desai Cancer Research centre, &#13;
Rajkot and hospital staff for providing necessary &#13;
samples.
</summary>
<dc:date>2017-01-01T00:00:00Z</dc:date>
</entry>
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