Rodolfo Brenner

Last updated
Rodolfo Brenner
Rodolfo Roberto Brenner
Retrato de Rodolfo R. Brenner.tif
Born17 July 1922
Died7 March 2018 (aged 95)
CitizenshipFlag of Argentina.svg  Argentina
Alma mater
Awards
Scientific career
Institutions
Thesis Composición química de aceites de oliva argentinos  (1946)
Doctoral advisor Pedro Cattaneo

Rodolfo Roberto Brenner was an Argentine emeritus professor of chemistry. [1] He was the founder and director of the Institute of Biochemical Research of La Plata and the co-founder of the Argentine Society for Biochemical Research. [2] [3] [4] [5]

Contents

Life and education

Rodolfo Brenner was born on July 17, 1922, at Banfield, Buenos Aires Province of Argentina. [1] In 1940 and  1946 he graduated as the best B. Sc and PhD chemistry student at the Colegio Nacional de Buenos Aires and the University of Buenos Aires winning gold medals for his performances [4] [2] [1]

Career

Rodolfo Brenner started as a graduate assistance till he became a professor. He worked as a Chairman of Bromatology and Industrial Analysis of the Faculty of Exact, Physical and Natural Sciences of the University of Buenos Aires between 1946 and 1954. Consequently, he was the one in charge of Industrial Toxicology Section at the Institute of Medical-Technological Research and the Institute of Public Hygiene where he studied the lipid composition of different river fish and he supervised five doctoral students. [3] [1]

In his last year as the chair of Bromatology and Industrial Analysis, he was awarded a British Council Postdoctoral Fellowship to work on "lipid chemistry and biochemistry" with Professor John Arnold Lovern at the Torry Research Institute in Aberdeen in Scotland. He returned in 1956 and became a full professor at the Faculty of Medical Sciences of the National University of La Plata. He became emeritus professor in 1998, the director of National Council for Scientific and Technical Research and institute of Physiology in 1968 and 1971 respectively. [2] [3]

Awards and honours

Rodolfo Brenner received Skibb 1950 gold medal, the Campomar Foundation Award in 1972, G. Burns and Von Euler gold medal in 1985, Konex Award in 1983; Alfredo Sordelli prize in 1985 and JJ Kyle award in 1990 . [1] He also received the “Supelco AOCS Research Award” from the American Oil Chemists' Society, in Baltimore, US, in 1990 [6] In 2001, he won the TWAS Basic Medical Sciences award for leading a research on the resolution of the mechanism of polyunsaturated fatty acid biosynthesis in animals and their regulation by dietary components and hormones and their biochemical and physiological effects. In 2006, he won the Bernardo Houssay Award. [7] [8]

Selected publications

Related Research Articles

<span class="mw-page-title-main">Lipid</span> Substance of biological origin that is soluble in nonpolar solvents

Lipids are a broad group of organic compounds which include fats, waxes, sterols, fat-soluble vitamins, monoglycerides, diglycerides, phospholipids, and others. The functions of lipids include storing energy, signaling, and acting as structural components of cell membranes. Lipids have applications in the cosmetic and food industries, and in nanotechnology.

<span class="mw-page-title-main">Triglyceride</span> Any ester of glycerol having all three hydroxyl groups esterified with fatty acids

A triglyceride is an ester derived from glycerol and three fatty acids. Triglycerides are the main constituents of body fat in humans and other vertebrates as well as vegetable fat. They are also present in the blood to enable the bidirectional transference of adipose fat and blood glucose from the liver and are a major component of human skin oils.

Essential fatty acids, or EFAs, are fatty acids that are required by humans and other animals for normal physiological function that cannot be synthesized in the body.⁠ As they are not synthesized in the body, the essential fatty acids – alpha-linolenic acid (ALA) and linoleic acid – must be obtained from food or from a dietary supplement. Essential fatty acids are needed for various cellular metabolic processes and for the maintenance and function of tissues and organs. These fatty acids also are precursors to vitamins, cofactors, and derivatives, including prostaglandins, leukotrienes, thromboxanes, lipoxins, and others.

<span class="mw-page-title-main">Eicosapentaenoic acid</span> Chemical compound

Eicosapentaenoic acid (EPA; also icosapentaenoic acid) is an omega−3 fatty acid. In physiological literature, it is given the name 20:5(n−3). It also has the trivial name timnodonic acid. In chemical structure, EPA is a carboxylic acid with a 20-carbon chain and five cis double bonds; the first double bond is located at the third carbon from the omega end.

<span class="mw-page-title-main">Docosahexaenoic acid</span> Chemical compound

Docosahexaenoic acid (DHA) is an omega−3 fatty acid that is an important component of the human brain, cerebral cortex, skin, and retina. It is given the fatty acid notation 22:6(n−3). It can be synthesized from alpha-linolenic acid or obtained directly from maternal milk (breast milk), fatty fish, fish oil, or algae oil. The consumption of DHA (e.g., from fatty fish such as salmon, herring, mackerel and sardines) contributes to numerous physiological benefits, including cognition. As a component of neuronal membranes, the function of DHA is to support neuronal conduction and to allow the optimal functioning of neuronal membrane proteins (such as receptors and enzymes).

<span class="mw-page-title-main">Bombykol</span> Sex pheromone of silk moths

Bombykol is a pheromone released by the female silkworm moth to attract mates. It is also the sex pheromone in the wild silk moth. Discovered by Adolf Butenandt in 1959, it was the first pheromone to be characterized chemically.

Fatty acid desaturases are a family of enzymes that convert saturated fatty acids into unsaturated fatty acids and polyunsaturated fatty acids. For the common fatty acids of the C18 variety, desaturases convert stearic acid into oleic acid. Other desaturases convert oleic acid into linoleic acid, which is the precursor to alpha-linolenic acid, gamma-linolenic acid, and eicosatrienoic acid.

Eicosatetraenoic acid (ETA) designates any straight chain tetra-unsaturated 20-carbon fatty acid. These compound are classified as polyunsaturated fatty acids (PUFA). The pure compounds, which are encountered rarely, are colorless oils. Two isomers, both of them essential fatty acids, are of particular interest:

Mycolic acids are long fatty acids found in the cell walls of Mycobacteriales taxon, a group of bacteria that includes Mycobacterium tuberculosis, the causative agent of the disease tuberculosis. They form the major component of the cell wall of many Mycobacteriales species. Despite their name, mycolic acids have no biological link to fungi; the name arises from the filamentous appearance their presence gives Mycobacteriales under high magnification. The presence of mycolic acids in the cell wall also gives Mycobacteriales a distinct gross morphological trait known as "cording". Mycolic acids were first isolated by Stodola et al. in 1938 from an extract of M. tuberculosis.

<span class="mw-page-title-main">Essential fatty acid interactions</span>

There is a wide variety of fatty acids found in nature. Two classes of fatty acids are considered essential, the omega-3 and omega-6 fatty acids. Essential fatty acids are necessary for humans but cannot be synthesized by the body and must therefore be obtained from food. Omega-3 and omega-6 are used in some cellular signaling pathways and are involved in mediating inflammation, protein synthesis, and metabolic pathways in the human body.

In biochemistry, fatty acid synthesis is the creation of fatty acids from acetyl-CoA and NADPH through the action of enzymes called fatty acid synthases. This process takes place in the cytoplasm of the cell. Most of the acetyl-CoA which is converted into fatty acids is derived from carbohydrates via the glycolytic pathway. The glycolytic pathway also provides the glycerol with which three fatty acids can combine to form triglycerides, the final product of the lipogenic process. When only two fatty acids combine with glycerol and the third alcohol group is phosphorylated with a group such as phosphatidylcholine, a phospholipid is formed. Phospholipids form the bulk of the lipid bilayers that make up cell membranes and surrounds the organelles within the cells. In addition to cytosolic fatty acid synthesis, there is also mitochondrial fatty acid synthesis (mtFASII), in which malonyl-CoA is formed from malonic acid with the help of malonyl-CoA synthetase (ACSF3), which then becomes the final product octanoyl-ACP (C8) via further intermediate steps.

<span class="mw-page-title-main">Mead acid</span> Chemical compound

Mead acid is an omega-9 fatty acid, first characterized by James F. Mead. As with some other omega-9 polyunsaturated fatty acids, animals can make Mead acid de novo. Its elevated presence in the blood is an indication of essential fatty acid deficiency. Mead acid is found in large quantities in cartilage.

<span class="mw-page-title-main">Acyl-(acyl-carrier-protein) desaturase</span> Class of enzymes

In enzymology, an acyl-[acyl-carrier-protein] desaturase (EC 1.14.19.2) is an enzyme that catalyzes the chemical reaction

<span class="mw-page-title-main">Linoleoyl-CoA desaturase</span> Class of enzymes

Linoleoyl-CoA desaturase (also Delta 6 desaturase, EC 1.14.19.3) is an enzyme that converts between types of fatty acids, which are essential nutrients in the human body. The enzyme mainly catalyzes the chemical reaction

<span class="mw-page-title-main">Stearoyl-CoA 9-desaturase</span> Class of enzymes

Stearoyl-CoA desaturase is an endoplasmic reticulum enzyme that catalyzes the rate-limiting step in the formation of monounsaturated fatty acids (MUFAs), specifically oleate and palmitoleate from stearoyl-CoA and palmitoyl-CoA. Oleate and palmitoleate are major components of membrane phospholipids, cholesterol esters and alkyl-diacylglycerol. In humans, the enzyme is present in two isoforms, encoded respectively by the SCD1 and SCD5 genes.

<span class="mw-page-title-main">FADS2</span> Enzyme found in humans

Fatty acid desaturase 2 (FADS2) is an enzyme that in humans is encoded by the FADS2 gene.

<span class="mw-page-title-main">FADS1</span> Enzyme found in humans

Fatty acid desaturase 1 (FADS1) is an enzyme that in humans is encoded by the FADS1 gene.

Sapienic acid is a fatty acid that is a major component of human sebum. Unique to humans, it takes its scientific name from the root sapiens. The equivalent fatty acid in mouse sebum is palmitoleic acid. Sapienic acid salts, esters, anion, and conjugate base are known as sapienates.

Delta12-fatty-acid desaturase (EC 1.14.19.6, Delta12 fatty acid desaturase, Delta12(omega6)-desaturase, oleoyl-CoA Delta12 desaturase, Delta12 desaturase, Delta12-desaturase) is an enzyme with systematic name acyl-CoA,hydrogen donor:oxygen Delta12-oxidoreductase. This enzyme catalyses the following chemical reaction

<span class="mw-page-title-main">Sciadonic acid</span> Chemical compound

Sciadonic acid, also known as eicosatrienoic acid, is a polyunsaturated fatty acid. In regard to its structure, 5Z,11Z,14Z-eicosa-5,11,14-trienoic acid has 3 double bonds in the 5, 11, and 14 positions all of which are in the cis configuration. It is further classified as Δ5-fatty, and an omega-6 acid due to the methylene interrupted double bond at carbon-5 and a final double bond 6 carbons away from the methylene tail of the hydrocarbon. Sciadonic acid is a naturally occurring compound and has been found to play a role as a plant metabolite, commonly found in pine nut oil. Furthermore, there have been propositions of several health applications for sciadonic acid as an anti-inflammatory agent. Sharing close structural similarity to arachidonic acid, sciadonic acid acts as a replacement phospholipid in the corresponding biochemical pathways.

References

  1. 1 2 3 4 5 "Dr. Rodolfo Brenner (1922-2018) – AAPC" (in Spanish). Retrieved 2022-12-10.
  2. 1 2 3 Factory, Troop Software. "Rodolfo Roberto Brenner | Fundación Konex". www.fundacionkonex.org (in Spanish). Retrieved 2022-12-10.
  3. 1 2 3 "Curriculum Vitae: Dr. Rodolfo Roberto Brenner". Acta Bioquímica Clínica Latinoamericana. 47 (2): 247. 2013. ISSN   0325-2957.
  4. 1 2 "Curriculum Vitae: Dr. Rodolfo Roberto Brenner". Acta bioquímica clínica latinoamericana. 47 (2): 247. 2013. ISSN   0325-2957.
  5. Leikin-Frenkel, Alicia I.; Garda, Horacio A. (2019-01-01). "Prof. Dr. Rodolfo R.Brenner 1922–2018 in memoriam" . Prostaglandins, Leukotrienes and Essential Fatty Acids. 140: 1–2. doi:10.1016/j.plefa.2018.11.010. ISSN   0952-3278. PMID   30553397. S2CID   58767405 . Retrieved 2022-04-05.
  6. "Supelco AOCS Research Award" (PDF).
  7. "Recipients of TWAS Awards and Prizes". TWAS. Retrieved 2022-12-10.
  8. "CEDIQUIFA - Listado Premios Bernardo Houssay". 2015-04-10. Archived from the original on 2015-04-10. Retrieved 2022-12-10.
  9. "Function and biosynthesis of lipids : [proceedings of the International Symposium on Function and Biosynthesis of Lipids held at Sierra de la Ventana, Tornquist, Province of Buenos Aires, Argentina, November, 1976] / edited by Nicolas G. Bazan, Rodolfo R. Brenner, and Norma M. Giusto".
  10. Brenner, Rodolfo R. (1981). "Nutritional and hormonal factors influencing desaturation of essential fatty acids" . Progress in Lipid Research. 20: 41–47. doi:10.1016/0163-7827(81)90012-6. PMID   7342101.
  11. 1 2 Brenner, Rodolfo R. (1984-01-01). "Effect of unsaturated acids on membrane structure and enzyme kinetics" . Progress in Lipid Research. 23 (2): 69–96. doi:10.1016/0163-7827(84)90008-0. ISSN   0163-7827. PMID   6093147.
  12. Brenner, R. (1984). "Effect of unsaturated acids on membrane structure and enzyme kinetics" . Progress in Lipid Research. 23 (2): 69–96. doi:10.1016/0163-7827(84)90008-0. PMID   6093147.
  13. Brenner, Rodolfo R. (1974). "The oxidative desaturation of unsaturated fatty acids in animals" (PDF). Molecular and Cellular Biochemistry. 3 (1): 41–52. doi:10.1007/BF01660076. PMID   4151182. S2CID   19234687.
  14. Brenner, Rodolfo R. (1971-08-01). "The desaturation step in the animal biosynthesis of polyunsaturated fatty acids" . Lipids. 6 (8): 567–575. doi:10.1007/BF02531137. ISSN   1558-9307. PMID   5094766. S2CID   34614186.
  15. Brenner, R. R. (1977). "Regulatory Function of Δ6 Desaturase — Key Enzyme of Polyunsaturated Fatty Acid Synthesis". Function and Biosynthesis of Lipids. Advances in Experimental Medicine and Biology. Vol. 83. pp. 85–101. doi:10.1007/978-1-4684-3276-3_8. ISBN   978-1-4684-3278-7. PMID   200115.
  16. Brenner, R. R. (1977), Bazán, Nicolás G.; Brenner, Rodolfo R.; Giusto, Norma M. (eds.), "Regulatory Function of Δ6 Desaturase — Key Enzyme of Polyunsaturated Fatty Acid Synthesis" , Function and Biosynthesis of Lipids, Advances in Experimental Medicine and Biology, vol. 83, Boston, MA: Springer US, pp. 85–101, doi:10.1007/978-1-4684-3276-3_8, ISBN   978-1-4684-3276-3, PMID   200115 , retrieved 2022-12-10