Search or add a thesis

Advanced Search (Beta)
Home > Overexpression of Aspartic Acid in Cotton Against Insects

Overexpression of Aspartic Acid in Cotton Against Insects

Thesis Info

Access Option

External Link

Author

Gul, Ambreen

Program

PhD

Institute

University of the Punjab

City

Lahore

Province

Punjab

Country

Pakistan

Thesis Completing Year

2019

Thesis Completion Status

Completed

Subject

Molecular Biology

Language

English

Link

http://prr.hec.gov.pk/jspui/bitstream/123456789/12402/1/Ambreen%20gul%20molecular%20biology%202019%20uop%20lhr%20prr.pdf

Added

2021-02-17 19:49:13

Modified

2024-03-24 20:25:49

ARI ID

1676726832332

Asian Research Index Whatsapp Chanel
Asian Research Index Whatsapp Chanel

Join our Whatsapp Channel to get regular updates.

Similar


Whitefly is a major threat to cotton production causing more than 60% yield losses to cotton crop. Owing to the limitations of whitefly control strategies through chemical insecticides, and lack of long term control offered by application of different strategies in the field of molecular biology instigates the establishment of new biochemical pathways pertaining to the whitefly resistance of the cotton plant. Current research work entails the enhancement of free aspartic acid in cotton by utilizing two different genes; OsAAT2 and ZmASN encodes aspartate and asparaginase proteins respectively. Both OsAAT2 and ZmASN genes were separately cloned in pCAMBIA-1301 vector under the control of CaMV35S promoter. Cotton variety CIM-482 was transformed through Agrobacterium tumefaciens (LBA4404) with a PCR-based transformation efficiency of 2.5%. Relative quantification of OsAAT2 and ZmASN transcripts by qRT-PCR depicted an increase of 31% and 48% respectively. UPLCbased quantification of amino acids in the transgenic cotton plants was assessed in the seeds of T0 and phloem sap of T1 progeny portraying an increase in amino acid concentrations. Aspartic acid concentration in the seeds of OsAAT2 and ZmASN transgenic cotton and non-transgenic control line was found to be 9.6mg/100g, 9.96mg/100g and 1.43mg/100g respectively. Similarly, an increase in the glutamic acid and asparagine concentration of 9.29mg/100g and 76mg/100g respectively in OsAAT2 transgenic line and 11.8mg/100g and 37mg/100g respectively in ZmASN transgenic line was observed in contrast to the non-transgenic control (3. 7mg/100g and 10.67 mg/100g). Free aspartic acid detected in the phloem sap of both OsAAT2 and ZmASN transgenic cotton lines revealed an increase of 3.48 x 10-2 mg and 2.19 x 10-2 mg respectively from the non-transgenic control cotton plant (0.845 x 10-2 mg). Different agronomic characters like height, number of bolls and yield of OsAAT2 and ZmASN transgenic cotton plants were analysed and exhibited an improvement in the aforementioned traits when compared with non-transgenic control plant. Agronomic characters of transgenic cotton like height, number of bolls and yield of transgenic cotton plants of OsAAT2 and ZmASN and non-transgenic control were also analysed and the results exhibited an improvement in the these traits when compared with non-transgenic control cotton plant. An improvement in height, number of bolls and yield was observed in the transgenic plants of OsAAT2 (192cm, 152 and 265g respectively) and ZmASN (149cm, 130 and 218g respectively) than the nontransgenic control (59cm, 23 and 50g). Cotton yield is determined in terms of quantity as well as quality. The quality of cotton fiber was determined by subjecting the cotton fiber to scanning electron microscope analysis for determination of fiber surface. Scanning electron microscopic analysis showed a fine surface of the transgenic cotton lines of both genes than the non-transgenic control cotton plants. The altered amino acid content has its direct influence on determination of plant physiology as was evident in case of transgenic cotton lines. The maximum increase in photosynthesis and stomatal conductance in transgenic lines of OsAAT2 was found to be (17.33 µmol m-2s- 1 and 322 mmol m-2s-1) and ZmASN (22 µmol m-2s-1 and 492 mmol m-2s-1) compared to non-transgenic control cotton line where it was found to be 9.56 and 37.66 respectively. More than 90% whitefly adult mortality was achieved in the transgenic cotton lines of both genes (OsAAT2 and ZmASN) as compared to the non-transgenic control cotton lines. Fluorescence in situ hybridization analysis of the advanced generation selected plant revealed that both genes were integrated as single copy gene in the plant genome at chromosome number 12 and 1 for OsAAT2 and ZmASN respectively.
Loading...
Loading...

Similar Books

Loading...

Similar Chapters

Loading...

Similar News

Loading...

Similar Articles

Loading...

Similar Article Headings

Loading...

مولوی عبدالحمید ندوی

مولوی عبدالحمید ندوی
یہ سطور ابھی پریس نہیں گئی تھیں کہ مولوی عبدالحمید ندوی کے انتقال کی خبر ملی، وہ بارہ بنکی کے ایک گاؤں جیسکھ پور کے رہنے والے تھے، بڑے مخلص، حق پسند اور بہی خواہ خلق تھے، ۱۹۱۹؁ء میں ندوہ میں داخل ہوئے، تحریک خلافت شباب پر تھی، حمید صاحب بھی اس سے متاثر ہوئے، اس کی وجہ سے سادگی طبیعت ثانیہ بن گئی، مولانا عبدالرحمن نگرامی کی صحبت نے ان کے اندر ندوہ کی محبت اور خاموش خدمت کا جذبہ پیدا کیا، تعلیم سے فراغت کے بعد قیام زیادہ تر وطن ہی میں رہا، لیکن ندوہ برابر آتے جاتے رہتے تھے، دوستوں کے اصرار کئی برس تک بھٹکل میں تعلیمی خدمت انجام دی، ان کے مخلص شاگردوں نے اس کام کو آگے بڑھایا اور ایک بڑا تعلیمی مرکز قائم ہوگیا، عرصہ سے دل کے مریض تھے، رمضان میں ندوہ آئے، مولانا ابوالحسن علی سے ملنے رائے بریلی جانے کا ارادہ تھا، دفعتہ دل کا دورہ پڑا اور تھوڑی دیر میں جان جان آفریں کے سپرد کردی، اﷲ تعالیٰ ان کی مغفرت فرمائے اور ان کے صاحبزادہ مولوی عبدالرشید ندوی اور دوسرے متعلقین کو صبر جمیل عطا فرمائے۔ (عبد السلام قدوائی، ستمبر ۱۹۷۸ء)

 

جهود علماء بهاولفور في النهضة العلمیة الحدیثة

The state of Bah┐walp┴r was founded in 1802 by Naw┐b Mohammad Bah┐wal Khan II. After the establishment of Pakistan the state opted to accede to the new, on 14 August 1947 October 1947. It was dominion of Pakistan, with effect from 7.1511 merged into the province of West Pakistan on 14 October Bah┐walp┴r has always been a seat of higher learning. Uch Shar┘f, a nearby ancient town, had one of the largest universities where scholars from all over the world used to come for studies. As a continuation of that tradition, J┐m‘a Abb┐siya was established in Bah┐walp┴r in the year 1925, following the academic pursuits of Jamia Al-Azhar, Egypt. The renowned scholars spread Islam by teaching Tafs┘r of Qura’n, Hadith, Fiqh, and History along with other contemporary subjects. The establishment of Jamia Abb┐sia and the arrival of religious scholars in Bah┐walp┴r bear witness that it is a scholarly and traditional state and it has been proved as a place of protection for educational, cultural and historical traditions.

Engineering Chloroplasts to Accumulate Antigenic Protein S to Immunize Poultry Birds Against Infectious Bursal Disease

Poultry industry is a dynamic sub-division of agriculture sector throughout the world as well as in Pakistan owing to rising global demand for this more affordable animal protein than red meat, due to exponential population growth and rapid urbanization in developing regions. However, the major problems encountered by the industry are infectious viral diseases; mainly infectious bursal disease (IBD), causing severe production and economic losses. Currently, live, attenuated or killed classical virus strains are used as vaccines to immunize birds but still outbreaks are reported even in vaccinated flocks probably owing to difference in antigenic structure between vaccine and field vvIBDV strains. Also, the current vaccine production systems including microbial, stable nuclear and transient plant viral technologies are not feasible in terms of cost and biosafety. So, as a preliminary step for development of clean quality and cost-effective recombinant subunit vaccine, a VP2 gene along with engineered choloroplast based Prrn promoter and PsbA terminator was synthesized commercially. Phylogenetic analysis and multiple sequence alignment with representative strains of different geographic origin confirmed the antigenic structure similarity of synthetic VP2 protein with those of circulating vvIBDV strains. Synthetic VP2 gene together with FLARE-S gene cassette was flanked by tobacco chloroplast flanking sequences through sequential cloning leading to development of final chloroplast transformation construct. Fully expanded 4-6 weeks old tobacco leaves were bombarded using a gene gun for chloroplast transformation. Initially, putative transplastomic lines regenerated on spectinomycin selection medium were selected by visual detection through gfp fluorescence as transplastomic sectors in a chimeric leaf tissue fluoresced green under UV light. These fluoresced sectors not only revealed heteroplasmic state of transgenic plants but also confirmed the successful integration of marker gene into tobacco chloroplasts. Putative transplastomic shoots were then subjected to additional rounds of selection and regeneration for developing homoplasmic clones. The genetic analysis of putative transplastomic plants through polymerase chain reaction confirmed the presence of VP2 as well as aada and gfp genes in the plastome. Integration of cassettes into inverted repeat region was confirmed using forward primer specific to aada gene and reverse primer specific to plastome. Further, development of an efficient regeneration system for soybean via somatic embryogenesis was attempted using 2 and 7 days old mature cotyledons from in-vitro germinated seedlings of a local ‘Faisal’ and an exotic ‘Jack’ cultivar with the intention to develop edible VP2 subunit vaccine as soybean is a chief constituent of poultry feed. It was observed that 7 days old mature cotyledonary explants of cultivar Jack were more responsive towards somatic embryogenesis than 2 days old ones and those of cultivar Faisal after callus induction on D20 medium directly. However, no regeneration was observed in either case indicating the need for further experimental investigation