147 research outputs found

    Enhancing Erucic Acid and Wax Ester Production in Brassica carinata through Metabolic Engineering for Industrial Applications

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    Metabolic engineering enables oilseed crops to be more competitive by having more attractive properties for oleochemical industrial applications. The aim of this study was to increase the erucic acid level and to produce wax ester (WE) in seed oil by genetic transformation to enhance the industrial applications of B. carinata. Six transgenic lines for high erucic acid and fifteen transgenic lines for wax esters were obtained. The integration of the target genes for high erucic acid (BnFAE1 and LdPLAAT) and for WEs (ScWS and ScFAR) in the genome of B. carinata cv. ‘Derash’ was confirmed by PCR analysis. The qRT-PCR results showed overexpression of BnFAE1 and LdPLAAT and downregulation of RNAi-BcFAD2 in the seeds of the transgenic lines. The fatty acid profile and WE content and profile in the seed oil of the transgenic lines and wild type grown in biotron were analyzed using gas chromatography and nanoelectrospray coupled with tandem mass spectrometry. A significant increase in erucic acid was observed in some transgenic lines ranging from 19% to 29% in relation to the wild type, with a level of erucic acid reaching up to 52.7%. Likewise, the transgenic lines harboring ScFAR and ScWS genes produced up to 25% WE content, and the most abundant WE species were 22:1/20:1 and 22:1/22:1. This study demonstrated that metabolic engineering is an effective biotechnological approach for developing B. carinata into an industrial crop

    (Lam.) Cogn. (Anchote) Biology, Productivity, and Prospects of Genetic Improvement Using Biotechnological Tools

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    Coccinia abyssinica (Lam.) Cogn. (local name anchote) is a tuber crop that belongs to the family Cucurbitaceae and it is cultivated for food and medicinal uses. It has relatively high quality of nutrient composition compared to other tuber crops, and is considered as the leading proteinous root crop with a high calcium content. Therefore, cooked anchote tubers are highly recommended for patients with broken or fractured bones. Anchote also contains alkaloids, phenols, tannins, flavonoids, and saponins. Although anchote is principally cultivated for its tubers, farmers prefer propagation by seeds as they are easy to store. Farmers select high-quality fruits for future seeds, based on the size of fruits and tubers. Since diseases and pests rarely affect the tubers, protection is not common. However, the fruit fly can damage the fruits, which predisposes them to decay. Although anchote has very high potential as a food security crop, it is neglected and underutilized and has received very limited research attention. Research published so far covers its ethnobotany, nutritional and anti-nutritional composition, traditional methods of reproduction, in vitro reproduction, somatic embryogenesis, anther breeding, and morphological and molecular genetic diversity. This article includes an analysis of previous and current research achievements, presents findings in a comprehensive way, and suggests future direction in crop improvement using biotechnological tools

    Micropropagation, transformation and genetic diversity of Hagenia abyssinica (Bruce) J.F. Gmel.

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    The tree species Hagenia abyssinica belongs to a monotypic genus in the family Rosaceae. It grows on the highlands of tropical Africa, where it is seriously endangered principally due to high timber demands. Therefore, the establishment of fast and efficient biotechnological methods to propagate and improve different traits of interest is much needed. The objectives of this study were to establish micropropagation and in vitro regeneration protocols and to transform this species with the rolB gene to improve the rooting efficiency. In addition, a study of genetic diversity was needed to provide information for in situ and ex situ conservation. A micropropagation protocol has been developed using explants from both juvenile and mature tree sources. These explants were initiated, multiplied and rooted using either WPM or MS medium and different combinations of BAP and IBA. Using leaves from in vitro grown shoots of juvenile or mature tree origin, an in vitro regeneration protocol has been developed based on using TDZ alone or in combination with NAA or 2,4-D. Regeneration efficiency was also studied using TDZ or BAP in combination with IAA. The effects of wounding, kanamycin and cefotaxime on regeneration have been studied. TDZ was found to be the best cytokinin for regeneration of H. abyssinica at low concentrations since it promotes direct shoot regeneration, as well as at high concentrations since it promotes callus induction and shoot regeneration although it inhibits shoot elongation. All auxins appeared to be toxic to H. abyssinica, particularly at higher concentrations. Based on the results of these regeneration experiments, H. abyssinica was transformed with the rolB gene. One clone of the transformants exhibited 77% rooting while no roots were produced by any of the untransformed control shoots. Kanamycin was found to be the main factor inhibiting the recovery of transformants whereas cefotaxime is toxic only at high concentrations. Since somaclonal variation of micropropagated plants is highly undesirable, genetic stability was tested on 80 micropropagated plants, 40 of axillary origin and 40 from adventitious shoots. These plants had been grown in vitro for over two years when they were screened with randomly amplified polymorphic DNA (RAPD) markers. Only one plant, originating from an axillary shoot, deviated by showing two extra bands thus indicating that H. abyssinica is relatively stable in vitro. A genetic diversity study based on inter simple sequence repeats (ISSR) was conducted on a total of 120 samples representing 12 populations from different parts of Ethiopia. This study showed that within- and between-population variability in H. abyssinica is typical of an outcrossed, perennial, late-successional species. Two recently planted populations and one indigenous primary forest-population showed the highest diversity. An autocorrelation analysis between genetic and geographic distances indicated that gene flow takes place over only about 30 km and this is likely to decrease even further because of genetic isolation among populations brought about by the current logging practices

    In vitro propagation of Ximenia americana L. from shoot tip explants: a multipurpose medicinal plant

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    Ximenia americana L. is among the most important multipurpose medicinal plants.It is highly vulnerable plant in Ethiopia due to overexploitation for different purposes, especially using the roots and barks for medicinal purposes.Seed germination is very poor and identical clones of superior quality plants cannot be obtained in nature as it is dioecious species. Therefore, the objective of this study was to develop in vitro propagation protocol for X. americana. After seed sterilization and germination, shoot tips from in vitro germinated seeds were cultured on ms (Murashige and Skoog) medium supplemented with different concentrations of benzyl amino purine (bap) or kinetin. For shoot multiplication, the initiated shoots were cultured on ms medium containing different concentrations of kinetin or bap in combination with a-naphthalene acetic acid (naa). Multiplied shoots were cultured on half strength ms medium supplemented with different concentrations of indole butyric acid (iba) or naa for rooting. The highest mean shoot number per explant (4.16 ± 0.17) was obtained on msmedium supplemented with 0.5 mg/l bap. The best rooting was obtained on half strength ms medium supplemented with 0.5 mg/l iba with 3.36 ± 0.69 roots per shoot and 2.21 ± 0.40 cm root length on medium containing 2.0 mg/l iba and established in greenhouse with 100% survival. The results of this study are important for mass propagation of superior genotypes, rehabilitation in natural habitat and conservation of this threatened multipurpose plant

    In Vitro Callus Induction and Shoot Regeneration from Leaf Explants of Glinus lotoides (L.)—An Important Medicinal Plant

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    G. lotoides L. is a threatened plant that is frequently harvested for medicinal purpose. However, its distribution in the world is limited because of short period of seed viability and poor seed germi-nation. The objective of this study was to develop in vitro propagation protocol for G. lotoides through callus induction. For callus induction, different concentrations of 2,4-D (2,4-dichloro-phenoxyacetic acid), NAA (α-naphthalene acetic acid) and BAP (6-benzyl amino purine) were used. Seeds were sown on growth regulator-free MS medium and shoots from the in vitro germinated seedlings were excised and cultured on MS medium containing 0.5 mg/l BAP. Young leaves from these shoots were used as explant for callus induction and shoot regeneration. Maximum callus induction (100%) was observed on medium containing 2,4-D (0.5, 2.0, 3.5 mg/l) or NAA (2.0, 2.5 mg/l) in combination with 0.5 mg/l BAP. However, 2,4-D was the best in overall callus induction. The highest regeneration (20%) frequency was achieved on the medium containing 0.5 mg/l BAP. Highest number of shoot (2.83 ± 1.22) and shoot length (2.16 ± 0.87 cm) per explant were ob

    Effect of growth regulators concentrations on in vitro multiplication of three elite sugarcane (Saccharum officinarum L.) Genotypes using shoot tip culture

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    Conventional vegetative propagation of sugarcane generally has low multiplication rate and allows distribution of diseases. Micropropagation is the only practical means of achieving rapid, large-scale production of disease-free quality planting material. Experiments on shoot tip culture initiation and shoot multiplication were laid out in completely randomized design with 2x3x3 and 4x5x3 factorial treatment arrangements respectively. Data were subjected to analysis of variance (ANOVA) and significant means were separated using Duncan's multiple range tests. With regard to shoot multiplication, genotype Q200 showed a maximum of 13.59 shoots per explant with 5.83cm shoot length on a medium fortified with 2 mg/l BAP alone, while genotype Q217 produced a maximum of 15.28 shoots per explant with 5.37cm mean shoot length on a medium supplied with 2.0 mg/l BAP and 0.25 mg/l kinetin. Likewise, Co-0238 produced a maximum of 13.56 shoots per explant with a mean shoot length 6.50 cm on medium fortified with 1.5 mg/l BAP + 0.5mg/l kinetin

    Phenotypic diversity of enset (Ensete ventricosum (Welw.) Cheesman) landraces used in traditional medicine

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    Enset (Ensete ventricosum (Welw.) Cheesman) is a multipurpose food security crop extensively cultivated in southern and southwestern parts of Ethiopia. In addition to its wide consumption as a source of food and feed, some enset landraces are also used as a traditional medicine in some parts of the country. However, the latter are becoming vulnerable to various human-related activities and environmental constraints. The main objective of this study was, therefore, to investigate the diversity that exist in enset landraces used for traditional medicine. A field study was conducted in four Administrative Zones and one special District in the Southern Nations, Nationalities and Peoples Region in Ethiopia. A total of 14 qualitative traits were employed to investigate the diversity in 40 landraces through field observation, color charts and focus group discussion. The data were analyzed using SAS and MINITAB softwares. Principal component analysis showed that the first four principal components accounted for 77% of the total variations and classified the landraces into four distinct groups. Similarly, cluster analysis grouped the landraces into four major clusters each containing 4–15 landraces. In general, the 14 phenotypic traits used in this study are important in discriminating the landraces indicating the existence of high genetic diversity among the landraces which needs to be conserved for the future

    Micropropagation of Glinus Lotoides L.: An Endangered Medicinal Plant

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    Glinus lotoides L., an endangered medicinal herb, is valued for its dietary vegetable and medicinal properties. It is propagated by seed. However, the seeds remain viable for very short period of time resulting in scarce distribution throughout the world. Hence, the objective of this study was to enhance germination of the seeds and to develop a micropropagation protocol for this plant. For seed germination experiment, Plant Growth Regulator (PGR) free MS (Murashige and Skoog) medium, filter paper and potted soil were used. Freshly harvested seeds from green house were sowed in PGR free MS medium to serve as explants. MS media containing different concentrations of 6-Benzyl Amino Purine (BAP) and Kinetin (KIN) were used for culture initiation and multiplication. Root induction was done on half strength MS medium containing different concentrations of Indole-3-Butyric Acid (IBA). Maximum ex vitro germination (73.77%) was obtained from fresh (0- day- old) seeds. The highest germination response (73.55%) was obtained from fresh (0- day- old) seeds sowed on MS medium. Highest shoot initiation (98.11%) was observed on medium containing 0.5 mg/l BAP. Best shoot multiplication (8.82 shoots per explant) was achieved on MS medium containing 0.5 mg/l BAP. Maximum shoot height (2.20 cm) was attained on PGR-free MS medium. Highest root number per shoot (6.86) with 96.67% rooting response was obtained in the presence of 0.5 mg/l IBA. Maximum root length (4.06 cm) was also achieved on this medium. The plantlets were transferred to sand-red soil-compost in 2:1:1 ratio and 87% of the plantlets survived after acclimatization. Thus, this study is useful for micropropagation of this medicinally important species. Keywords: Acclimatization, Rooting, Seed germination, Shoot multiplicatio
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