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University of Khartoum Graduate College Medical and Health Studies Board Activity
University of Khartoum Graduate College Medical and Health Studies Board Activity- guided Isolation and Structure Determination of Antioxidant and Antidiabetic Compounds from Bauhinia rufescence L. By: Wadah Jamal Ahmed Osman B. Pharm. U of K. (2003) M. Pharm. King Saud University (2012) A thesis submitted in fulfillment of the requirement for the degree of PhD in Pharmacognosy Supervisor Prof.Abdelkhaleig Muddathir, (B.Pharm.M.pharm., PhD) Professor of Pharmacognosy, U.of K. 2014 I Co-Supervisor: Prof. Dr. Hassan Elsubki Khalid B.Pharm., PhD Professor of Pharmacognosy, U.of K. II DEDICATION First of all I thank Almighty Alla for his mercy and wide guidance on a completion of my study. This thesis is dedicated to my parents, who taught me the value of education, to my beloved wife and to my beautiful kids. I express my warmest gratitude to my supervisor Professor Dr Prof. Abdelkhaleig Muddathir and Prof. Dr. Hassan Elsubki for their support, valuable advice, excellent supervision and accurate and abundant comments on the manuscripts taught me a great deal of scientific thinking and writing. In addition, I would like to express my appreciation to all members of the Pharmacognosy Department for their encouragement, support and help throughout this study. Great thanks for Professor Kamal Eldeen El Tahir (King Saud University, Riyadh) and Prof. Sayeed Ahmed (Jamia Hamdard University, India) for their co-operation and scientific support during the laboratory work. Wadah jamal Ahmed July, 2018 III Contents 1. Introduction and Literature review 1.1.Oxidative Stress and Reactive Metabolites 1 1.2. Production Of reactive metabolites 1 1.3. -
A Synopsis of Phaseoleae (Leguminosae, Papilionoideae) James Andrew Lackey Iowa State University
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1977 A synopsis of Phaseoleae (Leguminosae, Papilionoideae) James Andrew Lackey Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Botany Commons Recommended Citation Lackey, James Andrew, "A synopsis of Phaseoleae (Leguminosae, Papilionoideae) " (1977). Retrospective Theses and Dissertations. 5832. https://lib.dr.iastate.edu/rtd/5832 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. INFORMATION TO USERS This material was produced from a microfilm copy of the original document. While the most advanced technological means to photograph and reproduce this document have been used, the quality is heavily dependent upon the quality of the original submitted. The following explanation of techniques is provided to help you understand markings or patterns which may appear on this reproduction. 1.The sign or "target" for pages apparently lacking from the document photographed is "Missing Page(s)". If it was possible to obtain the missing page(s) or section, they are spliced into the film along with adjacent pages. This may have necessitated cutting thru an image and duplicating adjacent pages to insure you complete continuity. 2. When an image on the film is obliterated with a large round black mark, it is an indication that the photographer suspected that the copy may have moved during exposure and thus cause a blurred image. -
Middle to Late Paleocene Leguminosae Fruits and Leaves from Colombia
AUTHORS’ PAGE PROOFS: NOT FOR CIRCULATION CSIRO PUBLISHING Australian Systematic Botany https://doi.org/10.1071/SB19001 Middle to Late Paleocene Leguminosae fruits and leaves from Colombia Fabiany Herrera A,B,D, Mónica R. Carvalho B, Scott L. Wing C, Carlos Jaramillo B and Patrick S. Herendeen A AChicago Botanic Garden, 1000 Lake Cook Road, Glencoe, IL 60022, USA. BSmithsonian Tropical Research Institute, Box 0843-03092, Balboa, Ancón, Republic of Panamá. CDepartment of Paleobiology, NHB121, PO Box 37012, Smithsonian Institution, Washington, DC 20013, USA. DCorresponding author. Email: [email protected] Abstract. Leguminosae are one of the most diverse flowering-plant groups today, but the evolutionary history of the family remains obscure because of the scarce early fossil record, particularly from lowland tropics. Here, we report ~500 compression or impression specimens with distinctive legume features collected from the Cerrejón and Bogotá Formations, Middle to Late Paleocene of Colombia. The specimens were segregated into eight fruit and six leaf 5 morphotypes. Two bipinnate leaf morphotypes are confidently placed in the Caesalpinioideae and are the earliest record of this subfamily. Two of the fruit morphotypes are placed in the Detarioideae and Dialioideae. All other fruit and leaf morphotypes show similarities with more than one subfamily or their affinities remain uncertain. The abundant fossil fruits and leaves described here show that Leguminosae was the most important component of the earliest rainforests in northern South America c. 60–58 million years ago. Additional keywords: diversity, Fabaceae, fossil plants, legumes, Neotropics, South America. Received 10 January 2019, accepted 5 April 2019, published online dd mmm yyyy Introduction dates for the crown clades ranging from the Cretaceous to the – Leguminosae, the third-largest family of flowering plants with Early Paleogene, c. -
Evolution of Angiosperm Pollen. 7. Nitrogen-Fixing Clade1
Evolution of Angiosperm Pollen. 7. Nitrogen-Fixing Clade1 Authors: Jiang, Wei, He, Hua-Jie, Lu, Lu, Burgess, Kevin S., Wang, Hong, et. al. Source: Annals of the Missouri Botanical Garden, 104(2) : 171-229 Published By: Missouri Botanical Garden Press URL: https://doi.org/10.3417/2019337 BioOne Complete (complete.BioOne.org) is a full-text database of 200 subscribed and open-access titles in the biological, ecological, and environmental sciences published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Complete website, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/terms-of-use. Usage of BioOne Complete content is strictly limited to personal, educational, and non - commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Downloaded From: https://bioone.org/journals/Annals-of-the-Missouri-Botanical-Garden on 01 Apr 2020 Terms of Use: https://bioone.org/terms-of-use Access provided by Kunming Institute of Botany, CAS Volume 104 Annals Number 2 of the R 2019 Missouri Botanical Garden EVOLUTION OF ANGIOSPERM Wei Jiang,2,3,7 Hua-Jie He,4,7 Lu Lu,2,5 POLLEN. 7. NITROGEN-FIXING Kevin S. Burgess,6 Hong Wang,2* and 2,4 CLADE1 De-Zhu Li * ABSTRACT Nitrogen-fixing symbiosis in root nodules is known in only 10 families, which are distributed among a clade of four orders and delimited as the nitrogen-fixing clade. -
Desmodium Cuspidatum (Muhl.) Loudon Large-Bracted Tick-Trefoil
New England Plant Conservation Program Desmodium cuspidatum (Muhl.) Loudon Large-bracted Tick-trefoil Conservation and Research Plan for New England Prepared by: Lynn C. Harper Habitat Protection Specialist Massachusetts Natural Heritage and Endangered Species Program Westborough, Massachusetts For: New England Wild Flower Society 180 Hemenway Road Framingham, MA 01701 508/877-7630 e-mail: [email protected] • website: www.newfs.org Approved, Regional Advisory Council, 2002 SUMMARY Desmodium cuspidatum (Muhl.) Loudon (Fabaceae) is a tall, herbaceous, perennial legume that is regionally rare in New England. Found most often in dry, open, rocky woods over circumneutral to calcareous bedrock, it has been documented from 28 historic and eight current sites in the three states (Vermont, New Hampshire, and Massachusetts) where it is tracked by the Natural Heritage programs. The taxon has not been documented from Maine. In Connecticut and Rhode Island, the species is reported but not tracked by the Heritage programs. Two current sites in Connecticut are known from herbarium specimens. No current sites are known from Rhode Island. Although secure throughout most of its range in eastern and midwestern North America, D. cuspidatum is Endangered in Vermont, considered Historic in New Hampshire, and watch-listed in Massachusetts. It is ranked G5 globally. Very little is understood about the basic biology of this species. From work on congeners, it can be inferred that there are likely to be no problems with pollination, seed set, or germination. As for most legumes, rhizobial bacteria form nitrogen-fixing nodules on the roots of D. cuspidatum. It is unclear whether there have been any changes in the numbers or distribution of rhizobia capable of forming effective mutualisms with D. -
Oberholzeria (Fabaceae Subfam. Faboideae), a New Monotypic Legume Genus from Namibia
RESEARCH ARTICLE Oberholzeria (Fabaceae subfam. Faboideae), a New Monotypic Legume Genus from Namibia Wessel Swanepoel1,2*, M. Marianne le Roux3¤, Martin F. Wojciechowski4, Abraham E. van Wyk2 1 Independent Researcher, Windhoek, Namibia, 2 H. G. W. J. Schweickerdt Herbarium, Department of Plant Science, University of Pretoria, Pretoria, South Africa, 3 Department of Botany and Plant Biotechnology, University of Johannesburg, Johannesburg, South Africa, 4 School of Life Sciences, Arizona a11111 State University, Tempe, Arizona, United States of America ¤ Current address: South African National Biodiversity Institute, Pretoria, South Africa * [email protected] Abstract OPEN ACCESS Oberholzeria etendekaensis, a succulent biennial or short-lived perennial shrublet is de- Citation: Swanepoel W, le Roux MM, Wojciechowski scribed as a new species, and a new monotypic genus. Discovered in 2012, it is a rare spe- MF, van Wyk AE (2015) Oberholzeria (Fabaceae subfam. Faboideae), a New Monotypic Legume cies known only from a single locality in the Kaokoveld Centre of Plant Endemism, north- Genus from Namibia. PLoS ONE 10(3): e0122080. western Namibia. Phylogenetic analyses of molecular sequence data from the plastid matK doi:10.1371/journal.pone.0122080 gene resolves Oberholzeria as the sister group to the Genisteae clade while data from the Academic Editor: Maharaj K Pandit, University of nuclear rDNA ITS region showed that it is sister to a clade comprising both the Crotalarieae Delhi, INDIA and Genisteae clades. Morphological characters diagnostic of the new genus include: 1) Received: October 3, 2014 succulent stems with woody remains; 2) pinnately trifoliolate, fleshy leaves; 3) monadel- Accepted: February 2, 2015 phous stamens in a sheath that is fused above; 4) dimorphic anthers with five long, basifixed anthers alternating with five short, dorsifixed anthers, and 5) pendent, membranous, one- Published: March 27, 2015 seeded, laterally flattened, slightly inflated but indehiscent fruits. -
Fabaceae) Subfam
J. Jpn. Bot. 92(1): 34–43 (2017) Harashuteria, a New Genus of Leguminosae (Fabaceae) Subfam. Papilionoideae Tribe Phaseoleae a a b, Kazuaki OHASHI , Koji NATA and Hiroyoshi OHASHI * aSchool of Pharmacy, Iwate Medical University, Yahaba, Iwate, 028-3694 JAPAN; bHerbarium TUS, Botanical Garden, Tohoku University, Sendai, 980-0862 JAPAN *Corresponding author: [email protected] (Accepted on November 25, 2016) A new genus, Harashuteria K. Ohashi & H. Ohashi, is proposed as a member of the tribe Phaseoleae of Leguminosae (Fabaceae) based on Shuteria hirsuta Baker by comparative morphological observation and molecular phylogenetic analysis of Shuteria and its related genera. Molecular phylogenetic analysis was performed using cpDNA (trnK/matK, trnL–trnF and rpl2 intron) markers. Our molecular phylogeny shows that Shuteria hirsuta is sister to Cologania and is distinct from Shuteria vestita or Amphicarpaea, although the species has been attributed to these genera. A new combination, Harashuteria hirsuta (Baker) K. Ohashi & H. Ohashi is proposed. Key words: Amphicarpaea, Cologania, Fabaceae, Glycininae, Harashuteria, Hiroshi Hara, new genus, Phaseoleae, Shuteria, Shuteria hirsuta. The genus Shuteria Wight & Arn. was protologue. Kurz (1877) recognized Shuteria established on the basis of S. vestita Wight & hirsuta as a member of Pueraria, because he Arn. including 4–5 species in Asia (Schrire described Pueraria anabaptista Kurz citing 2005). The genus belongs to the subtribe S. hirsuta as its synonym (hence Pueraria Glycininae in the tribe Phaseoleae and is anabaptista is superfluous). Amphicarpaea closely allied to Amphicarpaea, Cologania, lineata Chun & T. C. Chen is adopted as a and Dumasia especially in the flower structures correct species by Sa and Gilbert (2010) in the (Lackey 1981). -
(Alhagi Maurorum) As New Sources of Bioactive Compounds Using GC-MS Technique
POJ 12(01):70-77 (2019) ISSN:1836-3644 doi: 10.21475/poj.12.01.19.pt1971 Assessment of camel thorn (Alhagi maurorum) as new sources of bioactive compounds using GC-MS technique Reham M. Mostafa, Heba S. Essawy* Botany Department, Facukty of Science, Benha University, Egypt Corresponding author: [email protected] Abstract Alhagi maurorum (A. maurorum) is one of the medicinally important plants belonging to the family leguminasae, commonly known as camel thorn. This research was amid to identify the chemical compounds in the aerial part of A. maurorum using GC-mass analysis. Three solvents with different polarities were used for the extraction of chemical constituents (water, methanol and petroleum ether). The results of GC-MS analysis led to identification of various compounds. In total, thirty-nine compounds from petroleum ether extract, thirty-two compounds in methanolic extract and seventeen compounds in aqueous extract were identified. Majority of the identified compounds have been reported to possess many biological activities. Among them, we reported 10 new anticancer compounds (Vitamin E; Hexadecanoic acid; Stigmast-5-en-3-ol; Phytol,2-hexadecen-1-ol,3,7,11,15-tetramethyl; Squalene; Hexadecanoic acid; 2-hydroxy-1-(hydroxymethyl) ethyl ester; Oxime,methoxy-phenyl,methyl N-hydroxyben- zenecarboximidoate; Ergost-5-en-3-ol; 9,12- Octadecad-ienoic acid and Farnesol) from A. maurorum using three solvent, while the best effective solvent was petroluem ether. Therefore, we report that A. maurorum has great potential to be developed into anticancer drugs. Keywords: Secondary metabolites; Alhagi maurarum; GC-mass spectroscopy; anticancer compounds. Introduction Natural products have useful and interesting biological tissue-repairing properties (Al-Snafi, 2015). -
The Plant Press
Department of Botany & the U.S. National Herbarium The Plant Press New Series - Vol. 17 - No. 1 January-March 2014 Botany Profile Research Scientist Spills the Beans By Gary A. Krupnick magine starting a new job by going population genetics to phylogenetics and rial of Psoraleeae and soybean (Glycine away on a three-month field excur- systematics. max). In 2007, Egan became a postdoc- sion to the remote forests of China, n 2001 she began her graduate years toral research associate in Doyle’s lab, I studying the phylogenetic systematics Japan, and Thailand after only two weeks at Brigham Young University, initially on the job, before having a chance to set- working on a doctoral thesis in cancer of subtribe Glycininae (Leguminosae). tle into your new office and unpack your I Egan’s research has determined that research. Her preliminary studies utilized boxes. Continue imagining that while phylogenetics as a means of bioprospect- tribe Psoraleeae is nested within subtribe you are away on your Asian expedition, ing, looking at the chemopreventive ability Glycininae, and is a potential progenitor you find out that your employer, the U.S. and phenolic content of the mint family, genome of the polyploid soybean. federal government, has shut down for 16 Lamiaceae. Unsatisfied with the direc- During her postdoctoral research, days, forcing you into “furlough in place” tion of her thesis, Egan switched to Keith Egan began collaborating with several status (non-duty and non-pay). Such is Crandall’s invertebrate biology laboratory, scientists studying soybean genome evo- the life of Ashley N. Egan, the Depart- with the understanding that Egan would lution. -
Fruits and Seeds of Genera in the Subfamily Faboideae (Fabaceae)
Fruits and Seeds of United States Department of Genera in the Subfamily Agriculture Agricultural Faboideae (Fabaceae) Research Service Technical Bulletin Number 1890 Volume I December 2003 United States Department of Agriculture Fruits and Seeds of Agricultural Research Genera in the Subfamily Service Technical Bulletin Faboideae (Fabaceae) Number 1890 Volume I Joseph H. Kirkbride, Jr., Charles R. Gunn, and Anna L. Weitzman Fruits of A, Centrolobium paraense E.L.R. Tulasne. B, Laburnum anagyroides F.K. Medikus. C, Adesmia boronoides J.D. Hooker. D, Hippocrepis comosa, C. Linnaeus. E, Campylotropis macrocarpa (A.A. von Bunge) A. Rehder. F, Mucuna urens (C. Linnaeus) F.K. Medikus. G, Phaseolus polystachios (C. Linnaeus) N.L. Britton, E.E. Stern, & F. Poggenburg. H, Medicago orbicularis (C. Linnaeus) B. Bartalini. I, Riedeliella graciliflora H.A.T. Harms. J, Medicago arabica (C. Linnaeus) W. Hudson. Kirkbride is a research botanist, U.S. Department of Agriculture, Agricultural Research Service, Systematic Botany and Mycology Laboratory, BARC West Room 304, Building 011A, Beltsville, MD, 20705-2350 (email = [email protected]). Gunn is a botanist (retired) from Brevard, NC (email = [email protected]). Weitzman is a botanist with the Smithsonian Institution, Department of Botany, Washington, DC. Abstract Kirkbride, Joseph H., Jr., Charles R. Gunn, and Anna L radicle junction, Crotalarieae, cuticle, Cytiseae, Weitzman. 2003. Fruits and seeds of genera in the subfamily Dalbergieae, Daleeae, dehiscence, DELTA, Desmodieae, Faboideae (Fabaceae). U. S. Department of Agriculture, Dipteryxeae, distribution, embryo, embryonic axis, en- Technical Bulletin No. 1890, 1,212 pp. docarp, endosperm, epicarp, epicotyl, Euchresteae, Fabeae, fracture line, follicle, funiculus, Galegeae, Genisteae, Technical identification of fruits and seeds of the economi- gynophore, halo, Hedysareae, hilar groove, hilar groove cally important legume plant family (Fabaceae or lips, hilum, Hypocalypteae, hypocotyl, indehiscent, Leguminosae) is often required of U.S. -
Combined Phylogenetic Analyses Reveal Interfamilial Relationships and Patterns of floral Evolution in the Eudicot Order Fabales
Cladistics Cladistics 1 (2012) 1–29 10.1111/j.1096-0031.2012.00392.x Combined phylogenetic analyses reveal interfamilial relationships and patterns of floral evolution in the eudicot order Fabales M. Ange´ lica Belloa,b,c,*, Paula J. Rudallb and Julie A. Hawkinsa aSchool of Biological Sciences, Lyle Tower, the University of Reading, Reading, Berkshire RG6 6BX, UK; bJodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, UK; cReal Jardı´n Bota´nico-CSIC, Plaza de Murillo 2, CP 28014 Madrid, Spain Accepted 5 January 2012 Abstract Relationships between the four families placed in the angiosperm order Fabales (Leguminosae, Polygalaceae, Quillajaceae, Surianaceae) were hitherto poorly resolved. We combine published molecular data for the chloroplast regions matK and rbcL with 66 morphological characters surveyed for 73 ingroup and two outgroup species, and use Parsimony and Bayesian approaches to explore matrices with different missing data. All combined analyses using Parsimony recovered the topology Polygalaceae (Leguminosae (Quillajaceae + Surianaceae)). Bayesian analyses with matched morphological and molecular sampling recover the same topology, but analyses based on other data recover a different Bayesian topology: ((Polygalaceae + Leguminosae) (Quillajaceae + Surianaceae)). We explore the evolution of floral characters in the context of the more consistent topology: Polygalaceae (Leguminosae (Quillajaceae + Surianaceae)). This reveals synapomorphies for (Leguminosae (Quillajaceae + Suri- anaceae)) as the presence of free filaments and marginal ⁄ ventral placentation, for (Quillajaceae + Surianaceae) as pentamery and apocarpy, and for Leguminosae the presence of an abaxial median sepal and unicarpellate gynoecium. An octamerous androecium is synapomorphic for Polygalaceae. The development of papilionate flowers, and the evolutionary context in which these phenotypes appeared in Leguminosae and Polygalaceae, shows that the morphologies are convergent rather than synapomorphic within Fabales. -
RNA-Seq Highlights Parallel and Contrasting Patterns in the Evolution of the Nuclear Genome of Fully Mycoheterotrophic Plants Mikhail I
Schelkunov et al. BMC Genomics (2018) 19:602 https://doi.org/10.1186/s12864-018-4968-3 RESEARCH ARTICLE Open Access RNA-seq highlights parallel and contrasting patterns in the evolution of the nuclear genome of fully mycoheterotrophic plants Mikhail I. Schelkunov1* , Aleksey A. Penin1,2,3 and Maria D. Logacheva1,4,5* Abstract Background: While photosynthesis is the most notable trait of plants, several lineages of plants (so-called full heterotrophs) have adapted to obtain organic compounds from other sources. The switch to heterotrophy leads to profound changes at the morphological, physiological and genomic levels. Results: Here, we characterize the transcriptomes of three species representing two lineages of mycoheterotrophic plants: orchids (Epipogium aphyllum and Epipogium roseum) and Ericaceae (Hypopitys monotropa). Comparative analysis is used to highlight the parallelism between distantly related fully heterotrophic plants. In both lineages, we observed genome-wide elimination of nuclear genes that encode proteins related to photosynthesis, while systems associated with protein import to plastids as well as plastid transcription and translation remain active. Genes encoding components of plastid ribosomes that have been lost from the plastid genomes have not been transferred to the nuclear genomes; instead, some of the encoded proteins have been substituted by homologs. The nuclear genes of both Epipogium species accumulated nucleotide substitutions twice as rapidly as their photosynthetic relatives; in contrast, no increase in the substitution rate was observed in H. monotropa. Conclusions: Full heterotrophy leads to profound changes in nuclear gene content. The observed increase in the rate of nucleotide substitutions is lineage specific, rather than a universal phenomenon among non-photosynthetic plants.