Abiogenesis – the Emergence of Life for the Very First Time
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Gas Chromatography-Mass Spectroscopy
Gas Chromatography-Mass Spectroscopy Introduction Gas chromatography-mass spectroscopy (GC-MS) is one of the so-called hyphenated analytical techniques. As the name implies, it is actually two techniques that are combined to form a single method of analyzing mixtures of chemicals. Gas chromatography separates the components of a mixture and mass spectroscopy characterizes each of the components individually. By combining the two techniques, an analytical chemist can both qualitatively and quantitatively evaluate a solution containing a number of chemicals. Gas Chromatography In general, chromatography is used to separate mixtures of chemicals into individual components. Once isolated, the components can be evaluated individually. In all chromatography, separation occurs when the sample mixture is introduced (injected) into a mobile phase. In liquid chromatography (LC), the mobile phase is a solvent. In gas chromatography (GC), the mobile phase is an inert gas such as helium. The mobile phase carries the sample mixture through what is referred to as a stationary phase. The stationary phase is usually a chemical that can selectively attract components in a sample mixture. The stationary phase is usually contained in a tube of some sort called a column. Columns can be glass or stainless steel of various dimensions. The mixture of compounds in the mobile phase interacts with the stationary phase. Each compound in the mixture interacts at a different rate. Those that interact the fastest will exit (elute from) the column first. Those that interact slowest will exit the column last. By changing characteristics of the mobile phase and the stationary phase, different mixtures of chemicals can be separated. -
22 Chromatography and Mass Spectrometer
MODULE Chromatography and Mass Spectrometer Biochemistry 22 Notes CHROMATOGRAPHY AND MASS SPECTROMETER 22.1 INTRODUCTION We know that the biochemistry or biological chemistry deals with the study of molecules present in organisms. These molecules are called as biomolecules and they form the basic unit of every cell. These include carbohydrates, proteins, lipids and nucleic acids. To study the biomolecules and to know their function, they have to be obtained in purified form. Purification of the biomolecules includes many physical and chemical methods. This topic gives about two of the commonly used methods namely, chromatography and mass spectrometry. These methods deals with purification and separation of biomolecules namely, protein and nucleic acids. OBJECTIVES After reading this lesson, you will be able to: z define the chromatography and mass spectrometry z describe the principle and important types of chromatographic methods z describe the principle and components of a mass spectrometer z enlist types of mass spectrometer z describe various uses of mass spectrometry 22.2 CHROMATOGRAPHY When we have a mixture of colored small beads, it is easily separated by visual examination. The same holds true for many chemical molecules. In 1903, 280 BIOCHEMISTRY Chromatography and Mass Spectrometer MODULE Mikhail, a botanist (person studies plants) described the separation of leaf Biochemistry pigments (different colors) in solution by using solid adsorbents. He named this method of separation called chromatography. It comes from two Greek words: chroma – colour graphein – to write/detect Modern separation methods are based on different types of chromatographic methods. The basic principle of any chromatography is due to presence of two Notes phases: z Mobile phase – substances to be separated are mixed with this fluid; it may be gas or liquid; it continues moves through the chromatographic instrument z Stationary phase – it does not move; it is packed inside a column; it is a porous matrix that helps in separation of substances present in sample. -
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BIO Web of Conferences 4, 00014 (2015) DOI: 10.1051/bioconf/20150400014 C Owned by the authors, published by EDP Sciences, 2015 From neonts to filionts and their progenies... Biodiversity draws its origins from the origins of life itself Marie-Christine Maurela Institut de Systématique, Évolution, Biodiversité (ISYEB - UMR 7205 – CNRS, MNHN, UPMC, EPHE), Muséum national d’Histoire naturelle, Sorbonne Universités, 45 rue Buffon, CP. 50, 75005 Paris, France “Should the question of the priority of the egg over the chicken, or of the chicken over the egg disturb you, it is because you assume that animals were originally what they are to-day; what madness!" The dream of d’Alembert, 1760, Denis Diderot Abstract. Since the origins, different modes of life exist. Indeed it is difficult to imagine how things could have been constructed by a single event that would have marked the birth of life. A brief historical background of the subject will be presented here. Then, we shall wander through the history of the discoveries that have led the way of experimental science over the last 150 years and shall dwell on one of the major paradigms, that of the RNA World. This paradigm illustrates the path followed by the living that tries all possible means when expressed at the molecular level as simple free molecule leading to RNA fragments and to modern subviral particles such as viroids then to ramifications and compartments. Between the ancient and the modern RNA world we underline how environment talks to molecules leading to the global living tissus which establish the ground of biodiversity. -
Coupling Gas Chromatography to Mass Spectrometry
Coupling Gas Chromatography to Mass Spectrometry Introduction The suite of gas chromatographic detectors includes (roughly in order from most common to the least): the flame ionization detector (FID), thermal conductivity detector (TCD or hot wire detector), electron capture detector (ECD), photoionization detector (PID), flame photometric detector (FPD), thermionic detector, and a few more unusual or VERY expensive choices like the atomic emission detector (AED) and the ozone- or fluorine-induce chemiluminescence detectors. All of these except the AED produce an electrical signal that varies with the amount of analyte exiting the chromatographic column. The AED does that AND yields the emission spectrum of selected elements in the analytes as well. Another GC detector that is also very expensive but very powerful is a scaled down version of the mass spectrometer. When coupled to a GC the detection system itself is often referred to as the mass selective detector or more simply the mass detector. This powerful analytical technique belongs to the class of hyphenated analytical instrumentation (since each part had a different beginning and can exist independently) and is called gas chromatograhy/mass spectrometry (GC/MS). Placed at the end of a capillary column in a manner similar to the other GC detectors, the mass detector is more complicated than, for instance, the FID because of the mass spectrometer's complex requirements for the process of creation, separation, and detection of gas phase ions. A capillary column is required in the chromatograph because the entire MS process must be carried out at very low pressures (~10-5 torr) and in order to meet this requirement a vacuum is maintained via constant pumping using a vacuum pump. -
A Production of Amino Acids Under Possible Primitive Earth Conditions
A Production of Amino Acids Under Possible Primitive Earth Conditions Stanley L. Miller Methods and Logic - 2/24/15 Outline for today’s class • The origin of life • Stanley L. Miller and Harold Urey • Background • Landmark Paper • Landmark Experiment • Subsequent Studies There are many theories regarding the origin of life • Theory of spontaneous generation: living organisms can arise suddenly and spontaneously from any kind of non-living matter • Aristotle, ancient Egyptians • Popular until 1600s when it was disproved due to various experiments • Fransisco Redi (1665) http://www.tutorvista.com/content/b iology/biology-iii/origin-life/origin- • Louis Pasteur (1864) life-theories.php# http://bekarice.com/college-spontaneous-generation/ There are many theories regarding the origin of life • Cozmozoic theory (parpermia): life reached Earth from other heavenly bodies such as meteorites, in the form of highly resistance spores of some organisms • Richter (1865) • Arrhenius (1908) • Overall lack of evidence Wikipedia • Living matter cannot survive the extreme cold, dryness and ultra-violet radiation from the sun required to be crossed for reaching the earth. There are many theories regarding the origin of life • Theory of chemical evolution: Origin of life on earth is the result of a slow and gradual process of chemical evolution that probably occurred about 4 billion years ago • Oparin (1923) • Haldone (1928) • Early Earth atmosphere (mixture of gases and solar radiation/lightning) • Miller-Urey Experiment Stanley L. Miller - Biography Born: 1930 in Oakland, CA Died: 2007 in San Diego, CA High school nickname: “a chem whiz” BS: UC Berkley - 1951 PhD: University of Chicago – 1954 (advisor: Harold Urey) California Institute of Technology Columbia University UC San Diego (1960-2007) National Academy of Sciences Landmark Paper: (1953) Production of amino acids under possible primitive earth conditions". -
Stanley L. Miller 1930–2007
Stanley L. Miller 1930–2007 A Biographical Memoir by Jeffrey L. Bada and Antonio Lazcano ©2012 National Academy of Sciences. Any opinions expressed in this memoir are those of the authors and do not necessarily reflect the views of the National Academy of Sciences. STANLEY L. MILLER March 7, 1930–May 20, 2007 Elected to the NAS, 1973 Stanley l. Miller, who was considered to be the father of prebiotic chemistry—the synthetic organic chemistry that takes place under natural conditions in geocosmochem- ical environments—passed away on May 20, 2007, at age 77 after a lengthy illness. Stanley was known worldwide for his 1950s demonstration of the prebiotic synthesis of organic compounds, such as amino acids, under simu- lated primitive Earth conditions in the context of the origin of life. On May 15, 1953, while Miller was a graduate student of Harold C. Urey at the University of Chicago, he published a short paper in Science on the synthesis of Stanley Miller Papers, the Mandeville of negavtive in The Register From at California University of the Geisel Library, Special Collection Library at 5. file 163, San Diego; MSS 642, box amino acids under simulated early Earth conditions. This paper and the experiment it described had a tremendous impact and immediately transformed the study of the By Jeffrey L. Bada origin of life into a respectable field of inquiry. and Antonio Lazcano Stanley Lloyd Miller was born in March 7, 1930, in Oakland, California, the second child (the first was his brother, Donald) of Nathan and Edith Miller, descendants of Jewish immigrants from the eastern European countries of Belarus and Latvia. -
Four Channel Liquid Chromatography/Electrochemistry
Four Channel Liquid Chromatography/Electrochemistry Bruce Peary Solomon, Ph.D. The new epsilon family of electrochemical detectors from BAS can Hong Long, Ph.D. Yongxin Zhu, Ph.D. control up to four working electrodes simultaneously. There are several Chandrani Gunaratna, Ph.D. advantages to using multiple detector electrodes. By using four different Lou Coury, Ph.D.* applied potentials with electrodes placed in a parallel arrangement, a Bioanalytical Systems, Inc. hydrodynamic voltammogram can be generated quickly through Corporate R&D Laboratories 2701 Kent Avenue acquisition of four data points for every analyte injection. This speeds West Lafayette, IN method development time. In addition, co-eluting compounds in complex 47906-1382 mixtures can be resolved on the basis of their observed half-wave * corresponding author potentials by using the same arrangement of electrodes, also in parallel. This article presents a few examples of four-electrode experiments performed with epsilon detectors in the BAS R&D labs during the past few months, using both radial-flow and cross-flow thin-layer configurations. The epsilon Platform the past fifteen years, our contract These instruments are fully network- research division, BAS Analytics, able and will be upgradable over the BAS developed and introduced the has provided analytical data of the Internet. New techniques and fea- first commercial electrochemical de- highest quality to the world’s leading tures may initially be ordered àla tector for liquid chromatography pharmaceutical companies using carte, or added at any time when the over twenty-five years ago. With this state-of-the-art products from BAS, need arises. In the coming months, issue of Current Separations,BAS as well as other leading vendors. -
Complexometric Titration and Atomic Emission Spectroscopy) That Allow Us to Quantify the Amount of Each Metal Present Individually
Title Quantitative Analysis of a Solution Containing Cobalt and Copper Name Manraj Gill (Lab partner: Tanner Adams) Abstract In this series of experiments, we determine the concentrations of two metal species, copper and cobalt, in a mixture of the two by initially using an ion exchange column to separate them from the mixture. We consequently use two different techniques (complexometric titration and atomic emission spectroscopy) that allow us to quantify the amount of each metal present individually. This step-by-step analysis not only goes through the basis for the experimental approach but also is a breakdown of the measurements that leads us to the final results: the Co:Cu ratio in the unknown mixture. Purpose In this series of three experiments (Parts I – III), we aim to initially separate a solution containing a mixture of Cobalt, Co (II), and Copper, Cu (II), ions in an unknown ratio and in unknown concentrations. The end goal of the entire experiment is to determine how much Co and Cu were originally present in the sample we obtained in Part I. But to do so, as explained in further detail in the ‘Theory and Methods’ section below, we initially separate the two ions (Part I) based on their unique chemical properties and then we attempt to quantify the separated ions through two different methods (Parts II, III). The overall purpose is an analysis of the efficiency of the separation and quantification approaches used to measure the constituent compounds in a mixture. This “efficiency” can be determined by comparing the obtained measurements to the known amounts that were used to make the solution. -
MILLER & UREY EXPERIMENT Could Organic Molecules Assemble
CLASSWORK: ORIGINS OF CELLS PERIOD: NAME: DATE: MILLER & UREY EXPERIMENT Could organic molecules assemble under conditions on early Earth? In 1953, chemists Stanley Miller and Harold Urey tried to answer that question. They filled a sterile flask with water, to simulate the early oceans, and boiled it. To the water vapor, they added methane, ammonia, and hydrogen to simulate the gasses that they thought were in the early atmosphere. Then, as shown in the diagram, they passed the gasses through electrodes to simulate lightning. Next, they passed the gasses through a condensation chamber, where cold water cooled them, causing liquid droplets to form and return to the starting flask. The liquid circulated through the experimental set up for 1 week. The results were spectacular. From these simple molecules, they produced 21 different amino acids – the building blocks of organic proteins. 1. Explain what each part of the experiment shown below represents. (Why did Miller & Urey include each component?) Part of the Experiment: What it Represents/Why it was Included: Heated Water Mix of Gasses (Methane, Ammonia, & Hydrogen) Electric Charge 2. What conclusions can Miller & Urey draw, based on their 1953 experiment? ______________________________________________________________________________________________________________ ______________________________________________________________________________________________________________ 3. We can say that the proteins in this experiment “self-assembled.” Based on your understanding of this experiment, -
Leslie E. Orgel 1927–2007
Leslie E. Orgel 1927–2007 A Biographical Memoir by Jack D. Dunitz and Gerald F. Joyce ©2013 National Academy of Sciences. Any opinions expressed in this memoir are those of the authors and do not necessarily reflect the views of the National Academy of Sciences. LESLIE ELEAZER ORGEL January 12, 1927–October 27, 2007 Elected to the NAS, 1990 Leslie Eleazer Orgel was a theoretical chemist and inves- tigator of the origins of life who made deep and lasting contributions in both of these scientific areas. He was born in London, England, on January 12, 1927, the second of three children of Simon and Deborah (Gnivisch) Orgel. His older brother Nevill was born on July 2, 1922, and died on December 28, 1957. His younger sister Delia was born on June 19, 1933, and currently resides in Silver Spring, Maryland. Leslie Orgel died on October 27, 2007, in San Diego, California, from pancreatic cancer. He is survived by his wife of 57 years, Alice (Levinson) Orgel; by his three children, Vivienne (b. April 4, 1955), Richard (b. November 29, 1956), and Robert (b. June 25, 1968); and by five By Jack D. Dunitz grandchildren. and Gerald F. Joyce After attending Dame Alice Owen’s School in London, which was evacuated during World War II to Bedford, England, Orgel studied chemistry at the University of Oxford, graduating in 1948 as BA with First Class Honours in Chem- istry. He then undertook graduate research with Leslie Sutton, senior chemistry tutor at Magdalen College and himself a distinguished physical chemist. Orgel’s1 first publication (1951) dealt with the semi-empirical calculation of electric dipole moments of conjugated heterocyclic molecules, and can be of no more than historical interest today. -
Separation Science - Chromatography Unit Thomas Wenzel Department of Chemistry Bates College, Lewiston ME 04240 [email protected]
Separation Science - Chromatography Unit Thomas Wenzel Department of Chemistry Bates College, Lewiston ME 04240 [email protected] LIQUID-LIQUID EXTRACTION Before examining chromatographic separations, it is useful to consider the separation process in a liquid-liquid extraction. Certain features of this process closely parallel aspects of chromatographic separations. The basic procedure for performing a liquid-liquid extraction is to take two immiscible phases, one of which is usually water and the other of which is usually an organic solvent. The two phases are put into a device called a separatory funnel, and compounds in the system will distribute between the two phases. There are two terms used for describing this distribution, one of which is called the distribution coefficient (DC), the other of which is called the partition coefficient (DM). The distribution coefficient is the ratio of the concentration of solute in the organic phase over the concentration of solute in the aqueous phase (the V-terms are the volume of the phases). This is essentially an equilibration process whereby we start with the solute in the aqueous phase and allow it to distribute into the organic phase. soluteaq = soluteorg [solute]org molorg/Vorg molorg x Vaq DC = --------------- = ------------------ = ----------------- [solute]aq molaq/Vaq molaq x Vorg The distribution coefficient represents the equilibrium constant for this process. If our goal is to extract a solute from the aqueous phase into the organic phase, there is one potential problem with using the distribution coefficient as a measure of how well you have accomplished this goal. The problem relates to the relative volumes of the phases. -
The Eightfold Path to Non-Enzymatic RNA Replication Jack W Szostak
Szostak Journal of Systems Chemistry 2012, 3:2 http://www.jsystchem.com/content/3/1/2 PERSPECTIVES Open Access The eightfold path to non-enzymatic RNA replication Jack W Szostak Abstract The first RNA World models were based on the concept of an RNA replicase - a ribozyme that was a good enough RNA polymerase that it could catalyze its own replication. Although several RNA polymerase ribozymes have been evolved in vitro, the creation of a true replicase remains a great experimental challenge. At first glance the alternative, in which RNA replication is driven purely by chemical and physical processes, seems even more challenging, given that so many unsolved problems appear to stand in the way of repeated cycles of non- enzymatic RNA replication. Nevertheless the idea of non-enzymatic RNA replication is attractive, because it implies that the first heritable functional RNA need not have improved replication, but could have been a metabolic ribozyme or structural RNA that conferred any function that enhanced protocell reproduction or survival. In this review, I discuss recent findings that suggest that chemically driven RNA replication may not be completely impossible. Keywords: Non-enzymatic replication, RNA World, protocell, origin of life, prebiotic chemistry, fidelity 1. Introduction assembly of ribonucleotides and RNA oligomers will Considerable evidence supports the RNA World hypoth- eventually be found. esis of an early phase of life, prior to the evolution of Unfortunately, even given prebiotically generated RNA coded protein synthesis, in which cellular biochemistry templates and abundant ribonucleotides, we do not under- and genetics were largely the province of RNA (reviewed stand how cycles of template-directed RNA replication in [1,2]).