Mary Helen Goldsmith

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Mary Helen Goldsmith
Alma materRadcliffe College
Scientific career
Thesis Characteristics of the translocation of indoleacetic acid in the coleoptile of Avena  (1960)

Mary Helen Goldsmith is a plant physiologist known for her work on how hormones impact plant growth. She is a fellow and past president of the American Society of Plant Physiologists.

Contents

Education and career

Goldsmith has a B.A. from Cornell University. [1] She earned her Ph.D. in 1960 from Radcliffe College where she researched the importance of indole acetic acid in the grass, Avena . [2] In 1963 she joined the faculty at Yale University where she worked until her retirement in 2006. [1]

Goldsmith was the director of the Marsh Botanical Garden for sixteen years and included visits to the garden in some of her classes. [1] [3] She also served as the president of the American Society of Plant Physiologists. [1]

Research

Goldsmith's early work was on impact of oxygen on insects. [4] During her Ph.D., she began to examine the movement of auxins, such as indole acetic acid, into corn. [5] [6] [7] She particularly focused on the polar diffusion of auxins. [8] [9] Her research extends to studies on changes in plant cells during transport of polar chemicals, [10] [11] intracellular measurements of membrane potential, [12] and activation of potassium channels. [13]

Selected publications

Awards and honors

Related Research Articles

<span class="mw-page-title-main">Plant hormone</span> Chemical compounds that regulate plant growth and development

Plant hormones are signal molecules, produced within plants, that occur in extremely low concentrations. Plant hormones control all aspects of plant growth and development, from embryogenesis, the regulation of organ size, pathogen defense, stress tolerance and through to reproductive development. Unlike in animals each plant cell is capable of producing hormones. Went and Thimann coined the term "phytohormone" and used it in the title of their 1937 book.

<span class="mw-page-title-main">Auxin</span> Plant hormone

Auxins are a class of plant hormones with some morphogen-like characteristics. Auxins play a cardinal role in coordination of many growth and behavioral processes in plant life cycles and are essential for plant body development. The Dutch biologist Frits Warmolt Went first described auxins and their role in plant growth in the 1920s. Kenneth V. Thimann became the first to isolate one of these phytohormones and to determine its chemical structure as indole-3-acetic acid (IAA). Went and Thimann co-authored a book on plant hormones, Phytohormones, in 1937.

<span class="mw-page-title-main">Cytokinin</span> Class of plant hormones promoting cell division

Cytokinins (CK) are a class of plant hormones that promote cell division, or cytokinesis, in plant roots and shoots. They are involved primarily in cell growth and differentiation, but also affect apical dominance, axillary bud growth, and leaf senescence.

Gibberellins (GAs) are plant hormones that regulate various developmental processes, including stem elongation, germination, dormancy, flowering, flower development, and leaf and fruit senescence. GAs are one of the longest-known classes of plant hormone. It is thought that the selective breeding of crop strains that were deficient in GA synthesis was one of the key drivers of the "green revolution" in the 1960s, a revolution that is credited to have saved over a billion lives worldwide.

<span class="mw-page-title-main">Coleoptile</span> Protective sheath in certain plants

Coleoptile is the pointed protective sheath covering the emerging shoot in monocotyledons such as grasses in which few leaf primordia and shoot apex of monocot embryo remain enclosed. The coleoptile protects the first leaf as well as the growing stem in seedlings and eventually, allows the first leaf to emerge. Coleoptiles have two vascular bundles, one on either side. Unlike the flag leaves rolled up within, the pre-emergent coleoptile does not accumulate significant protochlorophyll or carotenoids, and so it is generally very pale. Some preemergent coleoptiles do, however, accumulate purple anthocyanin pigments.

<span class="mw-page-title-main">Callus (cell biology)</span> Growing mass of unorganized plant parenchyma cells

Plant callus is a growing mass of unorganized plant parenchyma cells. In living plants, callus cells are those cells that cover a plant wound. In biological research and biotechnology callus formation is induced from plant tissue samples (explants) after surface sterilization and plating onto tissue culture medium in vitro. The culture medium is supplemented with plant growth regulators, such as auxin, cytokinin, and gibberellin, to initiate callus formation or somatic embryogenesis. Callus initiation has been described for all major groups of land plants.

<span class="mw-page-title-main">Gravitropism</span> Plant growth in reaction to gravity

Gravitropism is a coordinated process of differential growth by a plant in response to gravity pulling on it. It also occurs in fungi. Gravity can be either "artificial gravity" or natural gravity. It is a general feature of all higher and many lower plants as well as other organisms. Charles Darwin was one of the first to scientifically document that roots show positive gravitropism and stems show negative gravitropism. That is, roots grow in the direction of gravitational pull and stems grow in the opposite direction. This behavior can be easily demonstrated with any potted plant. When laid onto its side, the growing parts of the stem begin to display negative gravitropism, growing upwards. Herbaceous (non-woody) stems are capable of a degree of actual bending, but most of the redirected movement occurs as a consequence of root or stem growth outside. The mechanism is based on the Cholodny–Went model which was proposed in 1927, and has since been modified. Although the model has been criticized and continues to be refined, it has largely stood the test of time.

<span class="mw-page-title-main">Indole-3-acetic acid</span> Chemical compound

Indole-3-acetic acid is the most common naturally occurring plant hormone of the auxin class. It is the best known of the auxins, and has been the subject of extensive studies by plant physiologists. IAA is a derivative of indole, containing a carboxymethyl substituent. It is a colorless solid that is soluble in polar organic solvents.

<span class="mw-page-title-main">Xylan</span> A plant cell wall polysaccharide

Xylan is a type of hemicellulose, a polysaccharide consisting mainly of xylose residues. It is found in plants, in the secondary cell walls of dicots and all cell walls of grasses. Xylan is the third most abundant biopolymer on Earth, after cellulose and chitin.

Polar auxin transport is the regulated transport of the plant hormone auxin in plants. It is an active process, the hormone is transported in cell-to-cell manner and one of the main features of the transport is its asymmetry and directionality (polarity). The polar auxin transport functions to coordinate plant development; the following spatial auxin distribution underpins most of plant growth responses to its environment and plant growth and developmental changes in general. In other words, the flow and relative concentrations of auxin informs each plant cell where it is located and therefore what it should do or become.

<span class="mw-page-title-main">4-Chloroindole-3-acetic acid</span> Chemical compound

4-Chloroindole-3-acetic acid (4-Cl-IAA) is an organic compound that functions as a plant hormone.

In enzymology, an indole-3-acetaldehyde oxidase (EC 1.2.3.7) is an enzyme that catalyzes the chemical reaction

<span class="mw-page-title-main">Phototropism</span> Growth of a plant in response to a light stimulus

In biology, phototropism is the growth of an organism in response to a light stimulus. Phototropism is most often observed in plants, but can also occur in other organisms such as fungi. The cells on the plant that are farthest from the light contain a hormone called auxin that reacts when phototropism occurs. This causes the plant to have elongated cells on the furthest side from the light. Phototropism is one of the many plant tropisms, or movements, which respond to external stimuli. Growth towards a light source is called positive phototropism, while growth away from light is called negative phototropism. Negative phototropism is not to be confused with skototropism, which is defined as the growth towards darkness, whereas negative phototropism can refer to either the growth away from a light source or towards the darkness. Most plant shoots exhibit positive phototropism, and rearrange their chloroplasts in the leaves to maximize photosynthetic energy and promote growth. Some vine shoot tips exhibit negative phototropism, which allows them to grow towards dark, solid objects and climb them. The combination of phototropism and gravitropism allow plants to grow in the correct direction.

<span class="mw-page-title-main">Cholodny–Went model</span> Botany model

In botany, the Cholodny–Went model, proposed in 1927, is an early model describing tropism in emerging shoots of monocotyledons, including the tendencies for the shoot to grow towards the light (phototropism) and the roots to grow downward (gravitropism). In both cases the directional growth is considered to be due to asymmetrical distribution of auxin, a plant growth hormone. Although the model has been criticized and continues to be refined, it has largely stood the test of time.

Eleanor Beatrice Marcy "Beazy" Sweeney was an American plant physiologist and a pioneering investigator into circadian rhythms. At the time of her death she was professor emerita at the University of California, Santa Barbara, where she had worked since 1961.

Phytoprogestogens, also known as phytoprogestins, are phytochemicals with progestogenic effects.

Plants can be exposed to many stress factors such as disease, temperature changes, herbivory, injury and more. Therefore, in order to respond or be ready for any kind of physiological state, they need to develop some sort of system for their survival in the moment and/or for the future. Plant communication encompasses communication using volatile organic compounds, electrical signaling, and common mycorrhizal networks between plants and a host of other organisms such as soil microbes, other plants, animals, insects, and fungi. Plants communicate through a host of volatile organic compounds (VOCs) that can be separated into four broad categories, each the product of distinct chemical pathways: fatty acid derivatives, phenylpropanoids/benzenoids, amino acid derivatives, and terpenoids. Due to the physical/chemical constraints most VOCs are of low molecular mass, are hydrophobic, and have high vapor pressures. The responses of organisms to plant emitted VOCs varies from attracting the predator of a specific herbivore to reduce mechanical damage inflicted on the plant to the induction of chemical defenses of a neighboring plant before it is being attacked. In addition, the host of VOCs emitted varies from plant to plant, where for example, the Venus Fly Trap can emit VOCs to specifically target and attract starved prey. While these VOCs typically lead to increased resistance to herbivory in neighboring plants, there is no clear benefit to the emitting plant in helping nearby plants. As such, whether neighboring plants have evolved the capability to "eavesdrop" or whether there is an unknown tradeoff occurring is subject to much scientific debate. As related to the aspect of meaning-making, the field is also identified as phytosemiotics.

<span class="mw-page-title-main">Strigolactone</span> Group of chemical compounds

Strigolactones are a group of chemical compounds produced by roots of plants. Due to their mechanism of action, these molecules have been classified as plant hormones or phytohormones. So far, strigolactones have been identified to be responsible for three different physiological processes: First, they promote the germination of parasitic organisms that grow in the host plant's roots, such as Strigalutea and other plants of the genus Striga. Second, strigolactones are fundamental for the recognition of the plant by symbiotic fungi, especially arbuscular mycorrhizal fungi, because they establish a mutualistic association with these plants, and provide phosphate and other soil nutrients. Third, strigolactones have been identified as branching inhibition hormones in plants; when present, these compounds prevent excess bud growing in stem terminals, stopping the branching mechanism in plants.

The acid-growth hypothesis is a theory that explains the expansion dynamics of cells and organs in plants. It was originally proposed by Achim Hager and Robert Cleland in 1971. They hypothesized that the naturally occurring plant hormone, auxin (indole-3-acetic acid, IAA), induces H+ proton extrusion into the apoplast. Such derived apoplastic acidification then activates a range of enzymatic reactions which modifies the extensibility of plant cell walls. Since its formulation in 1971, the hypothesis has stimulated much research and debate. Most debates have concerned the signalling role of auxin and the molecular nature of cell wall modification. The current version holds that auxin activates small auxin-up RNA (SAUR) proteins, which in turn regulate protein phosphatases that modulate proton-pump activity. Acid growth is responsible for short-term (seconds to minutes) variation in growth rate, but many other mechanisms influence longer-term growth.

Peter Boysen Jensen was a Danish plant physiologist. His research was fundamental to further work on the auxin theory of tropisms.

References

  1. 1 2 3 4 "Mary Helen Goldsmith | Faculty of Arts and Sciences". fas.yale.edu. Retrieved 2022-01-03.
  2. Goldsmith, Mary Helen Martin (1960). Characteristics of the translocation of indoleacetic acid in the coleoptile of Avena (Thesis). OCLC   76986822.
  3. "Plants and Raves". Daily Nutmeg. 2013-05-30. Retrieved 2022-01-04.
  4. Goldsmith, Mary Helen M.; Schneiderman, Howard A. (1960). "The Effects of Oxygen Poisoning on the Post-Embryonic Development and Behavior of a Chalcid Wasp". The Biological Bulletin. 118 (2): 269–288. doi:10.2307/1539001. ISSN   0006-3185. JSTOR   1539001.
  5. Helen, Mary; Goldsmith, M.; Thimann, Kenneth V. (1962-07-01). "Some Characteristics of Movement of Indoleacetic Acid in Coleoptiles of Avena. I. Uptake, Destruction, Immobilization, & Distribution of IAA During Basipetal Translocation". Plant Physiology. 37 (4): 492–505. doi:10.1104/pp.37.4.492. ISSN   0032-0889. PMC   549821 . PMID   16655683.
  6. Goldsmith, Mary Helen M.; Wilkins, Malcolm B. (1964-03-01). "Movement of Auxin in Coleoptiles of Zea mays L. during Geotropic Stimulation". Plant Physiology. 39 (2): 151–162. doi:10.1104/pp.39.2.151. ISSN   0032-0889. PMC   550047 . PMID   16655890.
  7. Goldsmith, Mary Helen M. (1967-05-05). "Separation of Transit of Auxin from Uptake: Average Velocity and Reversible Inhibition by Anaerobic Conditions". Science. 156 (3775): 661–663. Bibcode:1967Sci...156..661G. doi:10.1126/science.156.3775.661. PMID   6023663. S2CID   36008743.
  8. Goldsmith, M H M (1977-06-01). "The Polar Transport of Auxin". Annual Review of Plant Physiology. 28 (1): 439–478. doi:10.1146/annurev.pp.28.060177.002255. ISSN   0066-4294.
  9. Goldsmith, M. H. M.; Goldsmith, T. H.; Martin, M. H. (1 February 1981). "Mathematical analysis of the chemosmotic polar diffusion of auxin through plant tissues". Proceedings of the National Academy of Sciences. 78 (2): 976–980. Bibcode:1981PNAS...78..976G. doi: 10.1073/pnas.78.2.976 . PMC   319928 . PMID   16592983.
  10. Cande, W. Z.; Goldsmith, Mary Helen M.; Ray, P. M. (1973). "Polar auxin transport and auxin-induced elongation in the absence of cytoplasmic streaming". Planta. 111 (4): 279–296. doi:10.1007/BF00385548. ISSN   0032-0935. PMID   24469695. S2CID   10659549.
  11. Goldsmith, Mary Helen M.; Ray, Peter M. (1973). "Intracellular localization of the active process in polar transport of auxin". Planta. 111 (4): 297–314. doi:10.1007/BF00385549. ISSN   0032-0935. PMID   24469696. S2CID   13558207.
  12. Goldsmith, Timothy H.; Goldsmith, Mary Helen M. (1978-01-01). "The interpretation of intracellular measurements of membrane potential, resistance, and coupling in cells of higher plants". Planta. 143 (3): 267–274. doi:10.1007/BF00391997. ISSN   1432-2048. PMID   24408464. S2CID   21287236.
  13. Spalding, Edgar P.; Goldsmith, Mary Helen M. (1993). "Activation of K⁺ Channels in the Plasma Membrane of Arabidopsis by ATP Produced Photosynthetically". The Plant Cell. 5 (4): 477–484. doi:10.2307/3869727. ISSN   1040-4651. JSTOR   3869727. PMC   160286 . PMID   12271073.
  14. "John Simon Guggenheim Foundation | Mary Helen Goldsmith" . Retrieved 2022-01-03.
  15. "272 TO SHARE $5.9 MILLION IN GUGGENHEIM AWARDS". The New York Times. 1986-04-13. ISSN   0362-4331 . Retrieved 2022-01-04.
  16. "Fellow of ASPB". American Society of Plant Biologists. Retrieved 2022-01-03.
  17. "ASPB Pioneer Members".