ABSTRACT
Nutrient allocation is central to understanding plant ecological strategies and forest roles in biogeochemical cycles. Thought to be mainly driven by environmental conditions, nutrient allocation to woody organs, especially to living tissues, is poorly understood. To examine the role of differences in living tissues (sapwood, SW, vs inner bark, IB), organs, ecological strategies, and environmental conditions in driving nutrient allocation and scaling in woody plants, we quantified nitrogen and phosphorus in main stems and coarse roots of 45 species from three tropical ecosystems with contrasting precipitation, fire regime, and soil nutrients. Nutrient concentration variation was mostly explained by differences between IB and SW, followed by differences between species and, in the case of phosphorus, soil nutrient availability. IB nutrient concentrations were four times those of SW, with root tissues having slightly higher concentrations than stem tissues. Scaling between IB and SW, and between stems and roots, was generally isometric. In cross-sections, IB contributed half of total nutrients in roots and a third in stems. Our results highlight the important role of IB and SW for nutrient storage, the coordination in nutrient allocation across tissues and organs, and the need to differentiate between IB and SW to understand plant nutrient allocation.
Subject(s)
Ecosystem , Nitrogen , Phosphorus , Plant Bark , Plant Leaves , Trees , Soil , Plant Roots , Plant StemsABSTRACT
The tropical tree Moringa oleifera produces high yields of protein-rich leaf biomass, is widely used as a food source, contains an abundance of phytochemicals, and thus has great potential for chronic disease prevention and perhaps, treatment. We have developed and characterized standardized ways of preparing aqueous "teas" from moringa leaves to deliver precisely calibrated levels of phytochemicals for use in clinical trials. These phytochemicals, especially the glucosinolate glucomoringin and the isothiocyanate moringin, produced from it following hydrolysis by the enzyme myrosinase, provide potent anti-inflammatory and cytoprotective indirect antioxidant activity. The taste of both hot and cold teas is palatable without the need for flavor masking. These teas can be easily and reproducibly prepared in underserved tropical regions of the world where moringa is cultivated. Isothiocyanate yield from a cold extraction was rapid and essentially complete after 30 min and its anti-inflammatory potential is comparable to that of equimolar purified moringin. A preparation similar to this may be safe to consume with respect to its bacterial titer even after 48 h without refrigeration. Thus, facile delivery of moringa tea to both adults and children for clinical evaluation of their effects on such conditions as autism, diabetes, and hypertension, is now possible.
Subject(s)
Glucosinolates/administration & dosage , Isothiocyanates/administration & dosage , Moringa oleifera/chemistry , Plant Leaves/chemistry , Administration, Oral , Animals , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/pharmacology , Beverages , Glucosinolates/chemistry , Isothiocyanates/chemistry , Macrophages/drug effects , Macrophages/metabolism , Mice , Molecular Structure , Nitric Oxide Synthase Type II/antagonists & inhibitors , Phytochemicals/chemistry , Phytochemicals/pharmacology , Plant Extracts/chemistry , Plant Extracts/pharmacology , RAW 264.7 CellsABSTRACT
Glucosinolates (GS) are metabolized to isothiocyanates that may enhance human healthspan by protecting against a variety of chronic diseases. Moringa oleifera, the drumstick tree, produces unique GS but little is known about GS variation within M. oleifera, and even less in the 12 other Moringa species, some of which are very rare. We assess leaf, seed, stem, and leaf gland exudate GS content of 12 of the 13 known Moringa species. We describe 2 previously unidentified GS as major components of 6 species, reporting on the presence of simple alkyl GS in 4 species, which are dominant in M. longituba. We document potent chemoprotective potential in 11 of 12 species, and measure the cytoprotective activity of 6 purified GS in several cell lines. Some of the unique GS rank with the most powerful known inducers of the phase 2 cytoprotective response. Although extracts of most species induced a robust phase 2 cytoprotective response in cultured cells, one was very low (M. longituba), and by far the highest was M. arborea, a very rare and poorly known species. Our results underscore the importance of Moringa as a chemoprotective resource and the need to survey and conserve its interspecific diversity.
Subject(s)
Chemoprevention/methods , Chronic Disease/prevention & control , Glucosinolates , Moringa/chemistry , Moringa/classification , Cells, Cultured , Cytoprotection/drug effects , Glucosinolates/chemistry , Glucosinolates/classification , Glucosinolates/isolation & purification , Glucosinolates/pharmacology , Humans , Magnetic Resonance Spectroscopy , Mass Spectrometry , Moringa oleifera/chemistry , Moringa oleifera/classification , Phylogeny , Phytotherapy/methods , Plant Extracts/pharmacology , Plant Leaves/chemistry , Plant Leaves/physiology , Seeds/chemistryABSTRACT
Taste drives consumption of foods. The tropical tree Moringa oleifera is grown worldwide as a protein-rich leafy vegetable and for the medicinal value of its phytochemicals, in particular its glucosinolates, which can lead to a pronounced harsh taste. All studies to date have examined only cultivated, domestic variants, meaning that potentially useful variation in wild type plants has been overlooked. We examine whether domesticated and wild type M. oleifera differ in myrosinase or glucosinolate levels, and whether these different levels impact taste in ways that could affect consumption. We assessed taste and measured levels of protein, glucosinolate, myrosinase content, and direct antioxidant activity of the leaves of 36 M. oleifera accessions grown in a common garden. Taste tests readily highlighted differences between wild type and domesticated M. oleifera. There were differences in direct antioxidant potential, but not in myrosinase activity or protein quantity. However, these two populations were readily separated based solely upon their proportions of the two predominant glucosinolates (glucomoringin and glucosoonjnain). This study demonstrates substantial variation in glucosinolate composition within M. oleifera. The domestication of M. oleifera appears to have involved increases in levels of glucomoringin and substantial reduction of glucosoonjnain, with marked changes in taste.