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العنوان
SEPARATION AND IDENTIFICATION OF OROBANCHE
SEEDS GERMINATION STIMULATORS THAT
PRODUCED BY ROOTS OF FABA BEAN \
المؤلف
MOHAMED, RASHA ABDEL KADER.
هيئة الاعداد
باحث / RASHA ABDEL KADER MOHAMED
مشرف / Ragy R. Francis
مشرف / Khaled M. A. Ramadan
مناقش / Sameh. E. Hassanein
تاريخ النشر
2014.
عدد الصفحات
67p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
علوم النبات
تاريخ الإجازة
1/1/2014
مكان الإجازة
جامعة عين شمس - كلية الزراعة - علوم زراعية
الفهرس
Only 14 pages are availabe for public view

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from 67

Abstract

V- SUMMARY
1- Faba bean (Vicia faba L.) is among the most cultivated crop legumes in the world. It is infected with a parasitic weed Orobanche spp. which is a root parasitic flowering plant devoid of chlorophyll which it causes important yield losses worldwide in several crops especially in food and feed legumes. Chemical, physical and biological control methods are used against this weed, but they are not usually enough effective.
2- Roots of the host plants produce germination stimulators of Orobanche spp seeds. The germinated seeds are then grow and attach to the root of the host plant forming an attachment organ that connects between the vascular tissues of the host and parasite. If the germinated Orobanche spp. seeds can’t found the host plants during only a few days, it will die.
3- In this study, root exudates of different four Faba bean varieties (two of them are resistant (Misr 1 and Giza 843) and two are sensitive (Nubaria and Misr 3) for the Orobanche infection) were collected and tested for its stimulation efficiency of Orobanche crenata seeds germination. Furthermore, the stimulation activity of the four Faba bean verities were tested by different methods including dual culture method in Petri dishes and pots using both conditioned and non-conditioned O. crenata seeds, under both growth chamber and green house conditions.
4- The highest O. crenata germination stimulation percentage (12%) was obtained from root exudates of Misr 1 Varity, under growth chamber conditions, using conditioned O. crenata seeds.
5- The germination stimulator was extracted from this root exudates by different solvents with gradient polarity, guided with testing of stimulation activity of each extract. Ethyl acetate extract showed stimulation of Orobanche crenata seeds germination.
6- This extract was purified by silica gel column, eluted with gradient mixture of hexane: ethyl acetate and acetone and methanol in two separate experiments. Each of the obtained extracts was analyzed by HPLC. One pure compound was obtained from the acetone fraction.
7- This pure compound was analyzed by NMR (H1, C13, APT, 2D H-H COSY and HMQC), Mass spectrometer and IR spectrometer for elucidation of its chemical structure. The spectral data showed that this compound is butyl, isobutyl phthalate.
8- Through this study, we strongly recommend using this compound in control of Orobanche spp. infestation