یونس فریدی: احوال و آثار
مکمل نام: محمد یونس
قلمی نام: یونس ؔفریدی
تخلص: یونس ؔ
پیدائش:
یونس ؔ ؔفریدی۴ اگست ۱۹۵۵ء بروز جمعرات شہرِ فریدؒ(پاکپتن شریف) کے محلہ ’’غلہ منڈی‘‘میں پیدا ہوئے۔ان کے والد کا نام چودھری ولی محمدہے۔ایک معزز آرائیں گھرانے سے تعلق رکھتے ہیں۔
شروع شروع میں ان کا نام’’محمد اصغر‘‘ رکھا گیا اور بلدیہ میں بھی اسی نام کا اندراج کروایا گیا۔ بعد میں سرداراں بی بی (پھوپھی) نے نام محمد یونس رکھا جو آج تک ان کی پہچان کا باعث ہے اور اسی نام سے پکارے جاتے ہیں۔(۱)
پھر بعد میں حضرت بابا فرید الدین مسعود گنج شکر رحمتہ اللہ علیہ کے ساتھ دلی عقیدت اور نسبت کے باعث نام کے ساتھ ’’فریدی‘‘ لکھنا شروع کیا۔یونسؔ فریدی اس بارے میں کہتے ہیں:
’’اپنے نام کے ساتھ فریدی میں نے خود ہی لکھنا شروع کردیا تھا۔ میرے ایک استادِ گرامی! نے پوچھا فریدی کے کیا معنی ہیں؟ اور تم نے کیوں لگایا ہے اپنے نام کے ساتھ؟ میں نے عرض کی جناب معنی تو مجھے نہیں معلوم لیکن مجھے یہ اچھا لگتا ہے۔سو میں نے لگا دیا۔ اور پھر بعد میں جب میرے شعور کی آنکھ کھلی تو میرا رجحان تصوف کی طرف ہو گیا۔ اور حضرت بابا فرید رحمتہ اللہ علیہ سے دلی عقیدت ہو گئی جو آج بھی ہے۔ اب تو مکمل فریدی ہو گیا ہوں۔ہاں بچپن میں اپنے والدِ گرامی کے ساتھ دربار شریف حاضری دیا کرتا تھا۔‘‘(۲)
یونس اپنے نام کے ساتھ فریدی لکھے بغیر اپنے نام کو ادھورا سمجھتے ہیں اور نام کے ساتھ فریدی لکھنا فخر محسوس کرتے ہیں۔یعنی محمد یونس سے تب سے اب تک محمد یونس ؔفریدی لکھنا اپنی اصل پہچان کا باعث سمجھتے ہیں۔
خاندانی پس ِ منظر:
جب یونس ؔ ؔفریدی کے شعور کی آنکھ کھلی تو وہ دیکھتے ہیں کہ ان...
Indonesian national low productivity of salt which is unequal between the need level and salt consumption eventually results in salt import made mainly to meet the industrial needs. The government through the Ministry of Marine Affairs and Fisheries has released a Public Salt Business Empowering Program (known as PUGAR/Pemberdayaan Usaha Garam Rakyat). PUGAR is an empowering program focusing on the improvement of job opportunities and welfare for salt farmers/managers to achieve the self-sufficiency of salt for consumptions and industries. This research aims at examining the influence of salt business empowering program on the salt farmers’ income improvement in Kedungmalang village of Jepara Regency; the implementation level of salt business empowering program in Kedungmutih Village of Demak Regency when compared to that in Kedungmalang Village of Jepara Regency; and the influence of salt business empowering program on the salt farmers’ income improvement in Kedungmutih village of Demak regency. The research was conducted using a descriptive method with a case study approach. The program implementation was quantitatively analyzed. Furthermore, the effectiveness of PUGAR on income was analyzed using T-test. The test result showed that there were income differences in Kedungmutih and Kedungmalang Village before and after the implementation of PUGAR. This finding showed that PUGAR was proven as an effective program to improve the salt farmers’ welfare through income improvement.
Chemical insecticides are widely used to control the insects, these insecticides are not environmentally healthy as they are not biodegradeable and hence are biomagnified. These insecticides are also not host specific; they also kill the beneficial insects. So there is a need to search for a control agent which should not harm the environment and also to human beings. Several different methods have been used in recent past to control the insects which include use of pheromones for trapping or disruption of mating behavior, insect growth regulators that interfere with larval development, parasitoids, fungi, viruses and bacteria, which debilitate or cause death in the infected insect. One of the most successful biological control organisms is a naturally occurring bacterial pathogen, Bacillus thuringiensis generally known as B.t. Formulations based on B.t. have been used for decades as biological insecticides for agriculture and forestry, as well as for vector control against mosquitoes and black flies. Interest in B.t. proteins has increased during the last two decades because of their unique qualities which are unmatched by any conventional insecticide. Of the 297 genes known to encode B.t. proteins, some share a high degree of homology, while others have diverse nucleotide sequences. Because of the interest in B.t., the list of new B.t. subspecies is growing as is the group of economically important target insects. B.t. produces crystal proteins during sporulation. These crystal proteins are of two types Cry and Cyt. Both of these types of proteins are different in their mode of action. Cytolytic proteins have an additional property of having cytolytic activity against different cells and also against mammalian erythrocytes. These proteins especially Cyt proteins are active against mosquito larvae. Recent studies reported the development of resistance in mosquitoes against Cry toxins. Researchers tried different methods to overcome this resistance and they found that when Cyt proteins are used in combination with Cry proteins they greatly reduced the resistance of mosquitoes against B.t. toxins. This indicated that Cyt proteins work synergistically with Cry proteins. In the present study, soil samples collected from different areas of Lahore, Kasur and Faisalabad. A total of 50 soil samples were collected, these soils were rich in organic manure. B.t. like bacteria were isolated from these soil samples using differential medium containing sodium acetate buffer. These isolates were then subjected to biochemical characterization by performing biochemical tests. The expected B.t. like isolates were screened for the presence of cyt genes. After confirmation of presence of cyt 2B gene, mosquitocidal activity of these isolates were checked by using B.t. spores and total B.t. cell proteins against 3rd instar larvae. From the bioassays, it was found that NB B.t.4 was found to be most toxic with LC50 value of 400±1.15 μg/ml and 68±0.46 μg/ml for its spores and total cell protein, respectively. After bioassays, six most toxic B.t. isolates were then selected for further study. Ribotyping of these isolates was done to amplifying 16S rRNA gene to identify these isolates. Protein profile of these isolates was checked to confirm the presence of 29 kDa protein band. Full length cyt 2B gene was amplified, cloned in pTZ57RT cloning vector, and pET22b vector was used for expression. IPTG induction of 1 mM was found good for expression ranging incubation time of 4-6 hours. Expressed protein was then purified by anion exchange chromatography. Bioassays were performed using recombinant organism (E. coli transformed with cyt 2B gene), expressed crude protein and purified protein. It was found that the purified protein was most toxic with LC50 Value of 50±1.68 μg/ml.