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Home > پاکستان میں مذہبی عدم برداشت اور میڈیا کے کردار کا تحقیقی و تجزیاتی مطالعہ

پاکستان میں مذہبی عدم برداشت اور میڈیا کے کردار کا تحقیقی و تجزیاتی مطالعہ

Thesis Info

Author

مراد فاطمہ

Supervisor

عبدالقدوس صہیب

Program

Mphil

Institute

Bahauddin Zakariya University

City

ملتان

Degree Starting Year

2017

Language

Urdu

Keywords

صحافت , تعریف و تاریخ , فقہی اختلافات

Added

2023-02-16 17:15:59

Modified

2023-02-19 12:20:59

ARI ID

1676731717604

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36. Ya. Sin./Yaseen

36. Ya. Sin./Yaseen

I/We begin by the Blessed Name of Allah

The Immensely Merciful to all, The Infinitely Compassionate to everyone.

36:01
a. Ya. Sin.

36:02
a. The Qur’an - full of Wisdom is an evidence of the fact that -

36:03
a. truly, you - O The Prophet - are of The Messengers,

36:04
a. - guided upon the Right Path,

36:05
a. it is a revelation being sent down onto you by The Almighty, The Infinitely Compassionate,

36:06
a. so that you can warn a people whose forefathers were never warned,
b. so they have remained heedless of the true faith and right guidance.

36:07
a. Indeed, the Word of misguidance is bound to be true against most of them, so they are not going to believe.

36:08
a. Indeed, WE have placed iron collars around their necks, up to their chins, so their heads are upturned, aloft and made stiff-necked so as not to see the Right Path.

36:09
a. And WE have set a barrier in front of them and a barrier behind them,
b. thus WE have blindfolded them from all sides in the darkness of ignorance so they can no longer see the light of truth and guidance.

36:10
a. Thus, it is all the same to them whether you warn them, or do not warn them,
b. they are not going to believe.

36:11
a. However, you can only warn someone who
- follows the Reminder – The Qur’an - and
- remains in awe of The Immensely Merciful despite not...

عصر حاضر کی تناظر میں عرف اور عادت کی شرعی حیثیت: ایک تجزیاتی مطالعہ

The unique feature of Islam is its comprehensive code of life. This proves its indispensability and worth as the universal order which accommodates complex issues of human life without compromising on its fundamentals. Hence, it is a matchless way of life on this planet. Keeping in view the modern specification of the current age in respect of those countries which tend to modify their legislations and their political, economic and social institutions as per Islamic framework. In this regard, a part from the fundamental and core Islamic sources of jurisprudence like the holy Quran, traditions of the holy Prophet (Hadith), consensus of Muslim scholars (Ijma) and Analogy (Qias), there are other sources like ‘Decorum’ (Istihsan) and ‘Arbitrariness’ (Masalih e Mursalah) to play their effective and significant jurisprudential role to address the numerous social issues by honoring the customs and norms already prevailing in any particular society. The article under discussion speaks of the distinct characteristic of Islam that it is a religion of nature and takes care of natural necessities of human life. Already prevailing customs and norms in human society are not subject to disregard or straight rejection. Islam puts a considerable endeavor not to confront the wisdom of the society by sweeping its norms and customs unnecessarily. Conditions imposed by Islam to formulate any society are specious enough which accommodate many of the customs and encompass overwhelming norms in it. But being the sincere guardian of the humanity, on the other hand, it does not miss its significant reformative role to play with reference to those customs and norms which appear contrary to its fundamentals

Studies on Amylases from Locally Isolated Strains of Aspergillus and Their Characterization

Microbial amylases are as important in industrial processes as are proteases. Among the microbes, fungi are gaining repute for the production of amylases. Keeping this in view, the present study was carried out to isolate, identify, characterize and explore the biotechnological applications of indigenous fungal strains. The study began by reviving fungal cultures from the stock collection in our lab and six more fungi were further isolated from the contaminated starch-agar plates. The isolates identified on the basis of cultural and morphological characteristics belonged to genus Aspergillus, Penicillium and Rhizopus. Preliminary screening was performed on starch-agar plate method with minor modification. Amylase production from the fungal isolates was also carried out under submerged fermentation conditions using mineral-salt media supplemented with starch and amylase production was quantitatively evaluated. Based on the results for quantitative production of amylases, 4 fungal isolates showing high IU/ml of amylase productivity were selected for further studies. The amylases from these isolates were characterized on the basis of activities at high temperatures and 2 fungal strains A. tubingensis SY 1 and A. niger MS 101 showing activities at 60oC and 64oC, respectively, were selected. Afterwards, the conditions for the optimum production of amylases from A. tubingensis SY 1 and A. niger MS 101 were worked out. The fungal strains showed optimum amylase production at 30oC with an initial pH of 5.9. Among the carbon sources; starch, glucose and maltose displayed higher amylase production along with the organic nitrogen source peptone. Amylase production was also optimized using a Plackett-Burman statistical design, and the results revealed peptone as the superior factor responsible for higher amylase titers. The optimum pH for amylase activity was determined along with the determination of optimum substrate concentration, the effect of various metal-ions and enzyme modulators. The pH 5.6 was optimum for amylase activity from both the fungal strains, while starch concentration of 0.5% was found to be optimum for the enzyme-substrate reaction to be carried out. Mn2+, K+ and NH4+ ions enhanced amylase activities while urea crystals and EDTA slightly inhibited the amylase activities of both fungal strains. Studies on solid-state fermentation (SSF) and submerged fermentation (SmF) for amylase production was also performed using variety of natural substrates including 2 halophytic plants and the results were compared. Whenever studies were compared with crude natural carbon substrates, whether under solid-state or submerged fermentation conditions together with the quantitative determination of amylase, the concentration of other enzymes, like xylanase, pectinase and cellulose enzyme system (β-glucosidase, endoglucanase, filter paper assay) were also determined. Potato-peels were found to be the most suitable substrate for amylase production by both fungal strains under SmF and SSF conditions. The Tm of amylase from the strain MS101 of A. niger was 65oC and from A. tubingensis SY 1 was 67oC, while Ea values were 73.64 KJ/mol and 46.07 KJ/mol for A. niger MS101 and A. tubingensis SY 1 amylases, respectively. Because of higher Tm values and low energies of activation (Ea) the industrial potential of amylases was determined. For this purpose, the starch-sized fabric was treated with fungal amylases at different temperatures for different time intervals to determine the d-sizing efficiency of amylases. The fabric after de-sizing by A. niger MS 101 amylase resulted in a TEGEWA rating of 8, while by A. tubingensis SY 1 amylase a TEGEWA rating of 9 was observed at 54oC in 12 hr. The results are promising for the use of these amylases in de-sizing. Co-culture studies for bioethanol production under SmF and SSF conditions were carried out using potato-peels under SmF and SSF, when the fermentation medium was simultaneously inoculated with the fungal and yeast strains, ~4 g/Kg and 6 g/Kg ethanol was produced in 120 hr. of incubation at 30oC. The yeast Pichia kudriavzevii SY 11 was also able to produce almost similar amount of ethanol under SmF of potatopeels. Indicating no contribution of fungal amylase to bioethanol. However, when coculture studies were carried out on purified starch 7- to 12- fold more ethanol production was noted (12 and 28 g/Kg) compared to potato-peel (1 and 4 g/Kg). Amylases were subjected to purification using different techniques: affinity and gelfiltration chromatography. No fruitful results were obtained by affinity chromatography while by using gel-filtration technique; a band of ~116 kDa was observed for A. tubingensis SY 1 amylase.