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1 CURRICULUM VITAE PERSONAL DATA: Name : Rehab Mahmoud Hafez Mahmoud Abdel-Rahman Profession : Assistant professor, Cytology and Genetics Division, Botany and Microbiology Department, Faculty of Science, Cairo University Address Work : Botany Department, Faculty of Science, Cairo University, Giza, Egypt E-mail Official : [email protected] Others : [email protected] [email protected] Phone Office : (+2) 3566671 (+2) 35676644 Mobile : (+2) 01006763263 (+2) 01203770993 Faculty official site: : scholar.cu.edu.eg/drrehabhafez LANGUAGES: Arabic (Mother Tongue) English (Excellent spoken, read & written, National TOEFL in 2000) French (Very good spoken, read & written) COMPUTER SKILLS: Very Good experience in computer common programs: Microsoft Office (Word, Excel and Power Point) and Photoshop. Basic IT Skills and Internet course (100 hours), Computers and Information Technology, Scientific Computation Center, Cairo University (11 June - 13 July 2006). Good experience in many computer programs for statistical analysis (eg: SPSS).

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1

CURRICULUM VITAE

PERSONAL DATA:

Name : Rehab Mahmoud Hafez Mahmoud Abdel-Rahman

Profession : Assistant professor, Cytology and Genetics Division,

Botany and Microbiology Department,

Faculty of Science, Cairo University

Address Work : Botany Department, Faculty of Science, Cairo University,

Giza, Egypt

E-mail Official : [email protected]

Others : [email protected]

[email protected]

Phone Office : (+2) 3566671 (+2) 35676644

Mobile : (+2) 01006763263 (+2) 01203770993

Faculty official site: : scholar.cu.edu.eg/drrehabhafez

LANGUAGES:

Arabic (Mother Tongue)

English (Excellent spoken, read & written, National TOEFL in 2000)

French (Very good spoken, read & written)

COMPUTER SKILLS:

Very Good experience in computer common programs: Microsoft Office (Word, Excel

and Power Point) and Photoshop.

Basic IT Skills and Internet course (100 hours), Computers and Information

Technology, Scientific Computation Center, Cairo University (11 June - 13 July 2006).

Good experience in many computer programs for statistical analysis (eg: SPSS).

2

OCCUPATIONS HISTORY:

Demonstrator (1/1997- 6/2006) - Botany and Microbiology Department - Faculty of

Science - Cairo University.

Assistant Lecturer (6/2006 -1/2013) - Botany and Microbiology Department - Faculty

of Science - Cairo University.

Assistant Professor (1/2013 till now) - Botany and Microbiology Department - Faculty

of Science - Cairo University.

EDUCATIONAL BACKGROUND:

B.Sc., 1996 (Botany; Very Good), Faculty of Science, Cairo University.

M.Sc., Jun, 2006 (Botany; Cytology, Genetics and Plant Biotechnology), Faculty of

Science, Cairo University, Egypt.

Titled: Production of solanum elaeagnifolium alkaloids ‘in vitro’ using plant tissue

culture techniques.

Abstract:

The present investigation was conducted to produce alkaloids of Solanum

elaeagnifolium using tissue culture techniques, which included: hairy roots cultures using

Agrobacterium rhizogenes strain ATCC 15834, callus cultures and regenerants.

The highest values of total steroidal alkaloids (TSA) (32.62 mg / g DW) and solasodine

(18.98 mg / g DW) were found in the fruit of the wild plant; much lower values were

recorded in other organs. Diosgenin was detected only in the roots (0.121 mg / g DW).

High values of TSA (10 mg / g DW) and solasodine (7.924 mg / g DW) were produced

from hairy roots developed on shoot explants infected with half strength MS medium

supplemented with bacteria and 10 ml acetosyringone. Diosgenin level was about 0.4

mg / g DW. Callus induction was performed using M2 medium (MS + 0.5 mg / L 2,4-D +

1.0 mg / L KIN) for root (R), hypocotyl (Hy), stem (St) and leaf (L) explants.

Effect of abiotic stresses (sodium chloride and mannitol); biotic stress (Aspergillus niger

extract) and some additives (cholesterol and reduced glutathione) were studied.

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Among callus cultures, the highest production of TSA (9.6 mg / g DW) was recorded in

St- and Hy-calli treated with 15 mM cholesterol, followed by (8.978 or 8.224 mg / g DW)

in R-calli treated with 40 % fungal extract or 0.05 M NaCl, respectively. Then came

L- and R-calli treated with 0.3 mM GSH (5.952 and 5.503 mg / g DW) and Hy-calli

treated with 0.11 M mannitol (5.032 mg / g DW). Regarding solasodine, St- and Hy-calli

treated with 15 mM cholesterol gave high values (4.582 and 4.265 mg / g DW,

respectively). Regarding diosgenin, the highest production (7.744 mg / g DW) was in

R-calli treated with 40 % fungal extract, followed by St-calli treated with 0.05 M NaCl

(3.049 mg / g DW). Regenerated shoots derived from apical shoot meristem contained

2.619 mg / g DW of TSA, which included equal amounts of solasodine and diosgenin

(about 0.55 mg / g DW). Regenerated plantlet and rooted-calli derived from

Hy-explants showed slight variation of TSA (2.429 and 2.835 mg / g DW, respectively).

The value of solasodine was higher than diosgenin in case of regenerated plantlet, while

the reverse was obtained in case of rooted-calli.

Ph.D., July, 2012 (Botany, Cytology, Genetics and Plant Biotechnology), Faculty of

Science, Cairo University, Egypt.

Titled: Improvement of fungal disease resistance in potato using Defensin gene and in

vitro selection.

Abstract:

Pathogenicity test showed that potato plants were highly susceptible to pathogenic

fungi Rhizoctonia solani, Fusarium dimerum, F. oxysporum, Cladosporium herbarum

and Nigrospora sphaerica. The maximum number of harvested tubers was found in case

of R. solani, while heavier tubers were in case of F. dimerum, F. oxysporum, N.

sphaerica and C. herbarum. The maximum number of tuber eyes was obtained in case of

C. herbarum. Nigrospora sphaerica and C. herbarum expressed wide variation in shapes,

colors and texture of tubers. The light microscopic observations showed changes in the

uppermost coat thickness and texture in all infected tissues compared with control.

Hypodermal tissue of infected tubers showed either hyperplasia in case of R. solani and

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F. dimerum or hypertrophy in case of F. oxysporum and C. herbarum. Most of the

infected tissues showed the presence of many cytoplasmic vacuoles in hypodermal and

cortical layers with the presence of few starch grains in the cortical cells compared to

those present in the non-infected tuber. Transmission electron microscopy investigations

showed cell wall and cytoplasmic changes and/or degradation, together with membrane

abnormalities. Most of the infected cells showed the deposition of densely opaque

granular material along the plasma membrane and/or tonoplast in addition to dark

inclusions and crystals. Microtuberization reached about 94% on Islam et al. medium

after 10 days. Multiple shoot regeneration from tuber discs (6.1±1.9) were enhanced on

Jarret et al. medium while Yee et al. medium was more efficient in case of leaf explants

(2.6±1.2) so; both media and explants were used in transformation experiments. RAPD

analysis was used to detect similarities or dissimilarities between the normal in vitro

plantlet and the regenerants. The in vitro plantlets were used as source of explants for

transformation and in vitro selection experiments. The tuber discs and leaf explants were

co-cultivated with Agrobacterium tumefaciens on regeneration medium supplemented

with acetoseryngone for 2 days then transfer to selection medium. The putative lines and

control plantlets were subjected histochemical analysis and specific PCR to confirm the

insertion of defensin gene and Gus reporter gene in them. In vitro selection was carried

out and only nodal cuttings exposed to successive rising of the concentration of the N.

sphaerica and C. herbarum exhibited resistance. In vitro plantlets, selected and

transformed lines were acclimatized. Resistance bioassay showed absence of symptoms

on transformed organs and some mild symptoms on the foliar lamina, tubers and calli of

the selected lines when exposed to N. sphaerica and C. herbarum infection units,

compared to those of in vitro plantlet. In vivo test showed that in vitro plants became

wilted with fragile leaves when exposed to R. solani, F. dimerum or F. oxysporum. In

case of N. sphaerica, no symptoms were seen, while in case of C. herbarum, the leaves

showed necrosis spots. Highest reduction in the external symptoms was observed in

transformed lines compared to the in vitro selected plantlets and in vitro plantlets.

5

SCIENTIFIC TRAINING COURSES ATTENDED:

WORKSHOPS in FACULTY and LEADERSHIP DEVELOPMENT

CENTER (FLDC):

Modern Methods in Plant Molecular Biology and Biochemistry,

provided by Plant Cell & Tissue Culture Department, Genetic

Engineering and Biotechnology Division, National Research

Center and Agricultural Analysis unit, Faculty of Agriculture,

Cairo University.

1998 March

Microanalysis and New Technology, Micro Analytical Center,

Faculty of Science, Cairo University. 2004 April

Molecular Biology Training Course, Development of Molecular

Biology Courses Project, Higher Education Enhancement Project

Fund (HEEPF), Faculty of Science, Cairo University.

2006 November

Molecular Genetics Approaches: Principles and Applications,

Molecular Biology Lab, Research Park (CURP), Faculty of

Agriculture, Cairo University.

4201 February

Gene Expression Analysis on Large Scale Using Microarray and

Real Time PCR Techniques, Molecular Biology Lab, Research

Park (CURP), Faculty of Agriculture, Cairo University.

4201 September

Thinking Skills 2006 July

New Trends in Teaching 0620 August

Quality Standards in Teaching 0920 May

Research Ethics 0920 December

International Scientific Publications 1020 May

Student Evaluation 1120 February

Effective Presentation 1201 June

Communication Skills 2201 January

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OTHER WORKSHOPS

Competing for Research Funds 2013 January

The Credit Hour Systems 2013 January

Conference Organization 2013 May

University Code of Ethics 2013 September

Legal and Financial Aspects in University Environment 2014 January

Managing Research Teams 2014 June

Effective Teaching Skills 2015 April

Statistical Analysis of Bio-Experiments 2017 March

Workshop on How to write proposal provided by Central Lab,

Ebn Sinai Hall, Faculty of Science, Cairo University. 2008 March

Training in course report and program provided by the Quality

Assurance and Accreditation Center, Ebn Sinai Hall, Faculty

of Science, Cairo University.

2011 January

Training in Key Performance Indicators- Ebn Sinai Hall,

Faculty of Science, Cairo University. 2015 November

Training in statistical methods- Ebn Sinai Hall, Faculty of

Science, Cairo University. 2015 November

Training in the principals of ISO 9001/2008 certification -Ebn

Sinai Hall, Faculty of Science, Cairo University. 2016 February

Training in academic advising - Cairo University Centre for

Quality Assurance of Education. 2017 January

Specification of the examination paper and the formulation of

the examination questions - Cairo University Centre for

Quality Assurance of Education.

2017 March

Preparing the specifications of the exam questions (blue 2017 March

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FIELDS OF INTERST:

Genetics, Cytology, Plant Tissue Culture, Transformation, Molecular Biology,

Mutations, Bioinformatics and Bio-Nanotechnology

TEACHING EXPERIENCES:

For Undergraduate Students:

Botany Courses: Genetics, Anatomy, Morphology, Physiology, Systematic, Ecology, Archegoniate,

Cell Biology, Phycology and Genetic Engineering in plants.

Microbiology courses General Microbiology, Environmental Microbiology, Mycology, Biotechnology,

Microbial enzymes, Virology, Biodiversity, Biological Control and Plant

Pathology.

For Postgraduate students (Applied Microbiology Diplomat):

Virology, Phycology and Environmental microbiology.

LABORATORY and TECHNICAL EXPERIENCES

Expert in techniques used to measure different physiological and biochemical

parameters such as Photosynthetic Pigments, Carbohydrates, Nucleic Acids, Protein

and Glycoalkaloids.

Expert in measuring the activity of some microbial enzymes.

Have good experience in preparation of samples for examination of cell divisions and

chromosomal abnormalities, and analyzing the observed phenomena.

Have some experience in how to prepare samples for TEM and analyzing the

observed phenomena.

print) - Cairo University Centre for Quality Assurance of

Education.

Measurement criteria for practical exams- Cairo University

Centre for Quality Assurance of Education.

2017 March

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Expert in Tissue Culture (Micropropagation, Callus Cultures, Cell Suspension, and

Organogenesis), in vitro selection and Agrobacterium-mediated transformation

Protocols.

Have good experience in Molecular Biology Protocols.

Have good experience in utilization of some bioinformatics tools.

Expert in isolation and culturing microorganisms (bacteria, fungi and actinomycetes)

and microalgae.

Have good experience in performing mutations of microbes and analyzing the

observed phenomena.

Have good experience in biofuel production using mechanical, chemical and

enzymatic pretreatments.

Proper utilization and maintenance of scientific instruments (PCR, Gel

Electrophoresis, Laminar Flow, Spectrophotometer, Autoclave, Digital Electrical

Balance, Cooling Centrifuge, pH meter, …etc..

PUBLICATIONS:

Mahmoud M. Saker, Salwa A. Abdel-Maksoud and Rehab M. Hafez (2006). In vitro

production of solasodine and diosgenin from hairy root cultures of Solanum

elaeagnifolium, In: 1st International Egyptian-Jordanian conference, p. 160 (abstract)

Mahmoud M. Saker, Salwa A. Abdel-Maksoud and Rehab M. Hafez (2006). Elicitation

of solasodine and diosgenin accumulation in callus cultures of Solanum

elaeagnifolium by Aspergillus niger culture filtrate, In: 1st International Egyptian-

Jordanian conference, p. 161 (abstract)

Salwa A. Abdel-Maksoud, Rehab M. Hafez, Mahmoud M. Saker and Mohamed K. El-

Bahr (2006). Effect of chemical additives on the production of steroidal alkaloids in

callus cultures of Solanum elaeagnifolium, In: 1st International Egyptian-Jordanian

conference, p. 156 (abstract)

Rehab M. Hafez, Salwa A. Abdel-Maksoud, Mahmoud M. Saker and El-Husseiny

Youssef (2006). Effect of salt and osmotic stresses on steroidal alkaloids content of

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Solanum elaeagnifolium callus cultures, In: 1st International Egyptian-Jordanian

conference, p. 157 (abstract)

Mahmoud M. Sakr, Amany H. A. Abo ELLil, Tarek A. A. Moussa, Rehab M. H. Abdel-

Rahman (2009). Development of Efficient regeneration System for Potato

Transformation, In: 3rd

International conference of Genetic Engineering and

Biotechnology Research Division (abstract).

Tarek A. A. Moussa, Mahmoud M.M. Saker, Nahed Z.M. Heikal, Amany H. A. Abo

ELLil, Rehab M. H. Abdel-Rahman (2010). Efficient transformation system for

fungal disease resistance in potato, In: 1st International Biotechnology Innovation

Conference, p. 51 (abstract).

Mahmoud M. Saker, Tarek A. A. Moussa, Nahed Z. Heikal, Amany H. A. Abo ELLil

and Rehab M. H. Abdel-Rahman (2012): Selection of an efficient in vitro

micropropagation and regeneration system for potato (Solanum tuberosum L.) cultivar

Desirée . African Journal of Biotechnology 11(98): 16388-16404.

SUPERVISION:

PhD Thesis (since 2015) in Microbiology, Microbiology Department, Faculty of science,

Ain Shams University.

MSc Thesis (since 2016) in Microbiology, Botany and Microbiology Department,

Faculty of science, Cairo University.

MSc Thesis (since 2016) in Cytology and Genetics, Botany and Microbiology

Department, Faculty of science, Cairo University.

MSc Thesis (since 2017) in Microbiology, Botany and Microbiology Department,

Faculty of science, Cairo University.

MEMBERSHIP OF SCIENTIFIC SOCIETIES:

1. Member in the Egyptian Botanical Society, Egypt

2. Member in the Egyptian Society of Experimental Biology, Egypt.

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CONFERENCES’ ATTENDENCE:

December 2006 : Participation in the 1st International Egyptian-Jordanian

Conference under the theme of "Biotechnology and

sustainable development: Current Status and Future

Scenarios", National Research Center, Cairo, Egypt

November 2009 : Participation in the 3rd

International conference of Genetic

Engineering and Biotechnology Research Division under the

theme of "Biotechnology For Better Life", National Research

Center, Cairo, Egypt

November 2010 : Participation in the 1st International Biotechnology Innovation

Conference (IBIC-Egypt 2010), Faculty of Science, Cairo

University, Cairo, Egypt

April 2011 : Attendance in the 7th

Annual International Conference of

Egyptian Society of Experimental Biology (ESEB-Egypt

2011), Faculty of Science, Cairo University, Cairo, Egypt

July 2011 : Attendance of the 2nd

International Workshop on Industrial

Biotechnology, Conference Center, Cairo University

April 2016 : Attendance in the 1st International Conference of Genetic

Engineering and Biotechnology: Integrative Science and

Biotechnology, Genetic Engineering and Biotechnology

Research Institute (GEBRI), University of Sadat City, Sharm

El Sheikh, Egypt

OTHER ACTIVITIES:

1. Member of Questionnaires Unit in Botany Department, Faculty of Science, Cairo

University, from 2004 to 2014.

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2. Performing poster and flier for Botany Department (2009) about its history and

sections, with Prof. Dr. Effat Shabana (Head of department) and revised by Prof. Dr.

Mohamed Ibrahim.

3. Performing flier for Botany Department (2012) about the pioneer and elites of our

Departments and the different work facilities of our graduates, with Prof. Dr. Tahany

Abdel-Rahman and other colleagues.

4. Member in the Postgraduates Tables Committee (Diploma, MSc, PhD) in Botany

Department from 2012 to 2015.

5. Executive Director of the Questionnaires Unit, Quality Assurance Unit, Faculty of

Science, Cairo University (2014-2015).

6. Member of Quality Assurance Unit in Botany Department, Faculty of Science, Cairo

University, (2006 to 2015): performing the courses’ specification and reports of the

postgraduate program in each term.

7. Work as general academic adviser for undergraduate students of the Faculty of

Science (2016).

8. Course specifications and course reports for undergraduate courses from 2012 till

now.

9. Member in some Committees in Botany Department (Library, Computer, Books and

Notes publications, from 2013 till now

10. Director of Questionnaires Unit, Quality Assurance Unit, Faculty of Science, Cairo

University, from 2015 till now.

11. Responsible of Quality Assurance Unit for Postgrades affairs in Botany Department,

Faculty of Science, Cairo University, from 2015 till now.

12. Work as a four year academic adviser for 10 undergraduate students of Biotechnology

program, from 2017 till now.

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AWARDS

- Certificate of Appreciation being the best assistant lecturer in Cairo university (2010).

- Certificate of Appreciation (6-2011) for outstanding performance from the Botany

Department, Faculty of Science, Cairo University.

- Certificate of Appreciation (4-2016) for outstanding efforts in enriching the figures of the

graduates in 2016, Faculty of Science, Cairo University.

ACADEMIC REFEREE

Prof. Dr. Abdel-Fattah Badr (Professor of Plant Genetics)

Botany & Microbiology Department, Faculty of Science, Helwan University, Cairo,

Egypt

e-mail: [email protected]

Prof. Dr. Mahmoud Sakr (Professor of Plant Biotechnology)

President of Academy of Scientific Research & Technology (ASRT), Kasr Al-Eini,

Cairo, Egypt.

e-mail: [email protected]

Prof. Dr. Tarek Abdel-Mawgoud Moussa (Professor of Microbiology)

Botany & Microbiology Department, Faculty of Science, Cairo University, Giza, Egypt.

e-mail: [email protected]

Prof. Dr. Tahany Abdel-Rahman (Professor of Microbiology)

Botany & Microbiology Department, Faculty of Science, Cairo University, Giza, Egypt.

e-mail: [email protected]

Prof. Dr. Maimouna Kord (Professor of Plant Physiology)

Botany & Microbiology Department, Faculty of Science, Cairo University, Giza, Egypt.

e-mail: [email protected]

Prof. Dr. Hasnaa Hosni (Professor of Taxonomy)

Botany & Microbiology Department, Faculty of Science, Cairo University, Giza, Egypt.

e-mail: [email protected]