Advancements in Life Sciences, volume 1, issue 3
Published online: 25-May-2014
ISSN 2310-5380
IN THIS ISSUE
Short Communication:
An overview of available Hypoglycemic Triterpenoids and Saponins to cure Diabetes mellitus
Dadu Khan Burdi, Sumera Qureshi, Allah Bux Ghanghro, pages 119-128
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Review Articles:
Nanotechnology: A new frontier in Agriculture
Muhammad Azam Ali, Iqra Rehman, Adnan Iqbal, Salah ud Din, Abdul Qayyum Rao, Ayesha Latif, Tahir Rehman Samiullah, Saira Azam, Tayyab Husnain, pages 129-138
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Genetically Modified Foods: Engineered tomato with extra advantages
Arfan Ali, Adnan Muzaffar, Mudassar Fareed Awan, Salah ud Din, Idrees Ahmad Nasir, Tayyab Husnain, pages 139-152
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Full Length Research Articles:
Microbiological stability of chemically preserved apricot pulp
Jabar Zaman Khan Khattak, Adil Hussain, Bilal Ahmad, Muhammad Fazal –Ul-Rehman, Zafar Ullah, Huma Arshad, Azhar Hussain, pages 153-159
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Method: The uniformly ripened Halman Apricot pulp was extracted and preserved by chemical preservatives such as Sodium Benzoate (SB), and Potassium Meta-Bisulphite (PMS) at different concentrations. The pulp was investigated for Microbiological parameters i.e. total bacterial count (TBC) and total fungal count (TFC). The inhibitory activity of chemical preservatives was tested periodically by simulating the industrial storage conditions for apricot pulp in the lab (30-42ºC in the dark), for a duration of 60 days.
Results: Significant inhibition in total bacterial count (TBC) was observed in chemically preserved samples. Potassium Metabisulphite was found to be more effective and the highest inhibitory effects on bacterial growth in apricot samples were observed at a concentration of 250mg/250g and 125mg/250g. These were followed by Sodium Benzoate at concentrations of 250mg/250g and 125mg/250g.
Conclusions: This study confirms that the preservatives significantly reduced bacterial and fungal growth in apricot pulp during storage and the pulp was safe for two months without spoilage.
Seasonal prevalence of eimeriosis in broiler chicken
Yasir Amin, Asim Aslam, Khurshaid Anwar, Pervez, Zubair Ali, pages 160-164
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Methods: The present study was conducted to know the round the year and seasonal prevalence of disease.During July 2012 to June 2013, a total of 1440 (n=1140) postmortem cases were carried out for disease diagnosis. Cases suspected for coccidiosis were confirmed by grass pathological lesions manifestation on the intestine and ceaca. Brief history including age, flock size was taken. For morphological examination, the oocytes were sieved and centrifuged at 3000 rpm with sugar solution.
Results: A total no of (n=1440) cases brought to outdoor patient services of Veterinary Research & Disease Investigation Centre, Abbott bad for disease diagnosis and treatment. Out of the total cases n=546 were found positive showing the overall prevalence of 37.91%.During hot and humid climatic conditions of monsoon season its prevalence was significantly high, during the month of August and September the observed infection percentage as 60.16% and 62.29 % respectively while low infection rate has been observed during the month of April which was 20.17%. Predominance of eimeriosis was high in young birds (3-4 weeks) and adult birds and less than 3 week of age birds was 74.90%, 17.94% and 7.14% respectively.
Conclusion: In present study, the higher prevalence of infection during the rainy season of monsoon observed indicating that warmth temperature and humid condition favors the oocytes sporulation and subsequent transmission.
Shakeela Daud, Saqib Shahzad, Muhammad Shafique, Munir Ahmad Bhinder, Muhammad Niaz, Asif Naeem, Azam Ali, Zia-ur-Rehman, Tayyab Husnain, pages 165-170.
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Methods: Blood samples of 86 individuals were drawn from 25 Pakistani families. DNA was extracted and purified by Sambrook method. DNA was quantified at agarose gel electrophoresis and N-D 1000 Nanodrop spectrophotometer. Three hypervariable regions (HVR I, HVR II and HVIII) of mitochondrial DNA were optimized with different PCR components and PCR conditions using three pairs of oligonucleotides along with reagent blanks, positive and negative controls.
Results: The best results for amplification were shown at 1x PCR buffer, 2.5mM Mgcl2, 0.3µl of Taq DNA polymerase (5u/µl), 0.2mM dNTPs, 0.8µM
forward-reverse primers for HVR I, 0.7µM forward-reverse primers for HVR II and 0.4µM forward-reverse primers for HVR III at 52◦C annealing temperature.
Conclusion: Optimized PCR protocol for three hypervariable mtDNA regions has provided a way out to lead mtDNA analysis which is very necessary tool in those forensic biological samples, where nuclear DNA is highly degraded, to identify missing persons and determine maternal lineages.
Disease free and rapid mass production of sugarcane cultivars
Ghulam Zahara Jahangir, Idrees Ahmad Nasir, Muhammad Iqbal, pages 171-180
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Methods: The source plants were sampled randomly from cane growing areas all over the country. Apical region from stalks of germinated plants was taken as explant source. The growth medium used for direct regeneration and multiple shoot formation was same for all constituents but the hormonal supplementations; it comprised of MS basal medium 4.43g/l (MS SIGMA, M 5519), 3% w/v sucrose, and phytagel was added in 0.3% w/v for gelling to support the explant, 0.01mg/l activated charcoal as the carbon source, pH 5.5 to 5.8.
Results: Among various concentrations of BAP used 1.0, 1.5 and 2.0mg/l in growth medium supported efficient regeneration and plenty of lateral shoots in a minimum time span almost in all cultivars. For rhizogenesis, 5.0mg/l of IAA was found to be most efficient among four different concentrations of auxin. Some cultivars have a sufficient endoauxin level and do not need any supplementation for rooting i.e., basal medium supports root induction. For long term maintenance of plant stock, MS broth with 1.0mg/l of BAP was found to be most suitable.
Conclusion: Cytokinin concentrations and plant potential play an equal role in direct regeneration from meristematic tissue.
Biochemical basis of resistance in rice against Bacterial leaf blight disease caused by Xanthomonas oryzae pv. oryzae
Junaid Ahmed Khan, Sehar Afroz, Hafiz M. Imran Arshad, Nighat Sarwar, Hafiza Sidra Anwar, Kamran Saleem, M Masood Babar, Farhat Fatima Jamil, pages 181-190
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Methods: Plants inoculated with Xanthomonas oryzae pv. oryzae isolates i.e. 78.3 and 2.2 caused disease on all varieties were selected for investigation of phenolic compound. Randomized complete block design was used in field for inoculation and leaf collections for phenolic compounds determination. Data was phenolic compounds were analyzed through factorial ANOVA.
Results: The response of four varieties was different when inoculated with BLB isolate 2.2. Basmati 2000 variety of rice produced maximum amount of phenolic compounds after one week of inoculation of bacterial isolate 2.2 while the minimum total phenols were found in basmati 385 at 0 hrs. of inoculation (before inoculation). Xoo isolate 78.3 produced maximum phenolic compounds after 2 weeks in Basmati 2000.
Conclusions: Biochemical resistance due to high phenolic contents in Basmati-385 and Basmati-2000 is suggested. High phenol production may be due to loss of virulence in bacterial isolates. Both 78.3 and 2.2 Xoo isolates are significantly different in producing total phenols in all the varieties tested.