RESEARCH PAPER ON BIOLOGICAL ACTIVITY OF ACTINOMYCETES ................ ABSTRACT: The microorganisms are ubiquitous in nature. They are found in probably every environmental condition present on earth. Actinomycetes were originally considered to be an intermediate group between bacteria and fungi but now are recognized as prokaryotic organisms with high G+C (>55%) content in their DNA. Our project aim is to evaluate some biological activities of Actinomycetes like:
Premium Enzyme Petroleum Bacteria
GRADE 11 CHEMISTRY (30S) Final Practice Examination Answer Key GRADE 11 CHEMISTRY (30S) Final Practice Examination Answer Key IInstructions The final examination will be weighted as follows Modules 1–3 Modules 4–6 The format of the examination will be as follows: Part A: Fill-in-the-Blanks Part B: Multiple Choice Part C: Short Answer Total Marks Include units with all answers as required. Useful Information You will need the following in order to complete this examination: n n n n 15–20% 80–85%
Premium Stoichiometry Atom Ion
Analysis of Alcohols‚ Aldehydes and Ketones Karl Wayne Mancao‚ Raphaell Mordeno‚ Andres Pastrana III*‚ and Shannen Peñaverde Department of Biology‚ University of Santo Tomas‚ Manila‚ Philippines Abstract The proponents have done several tests for identifying alcohols‚ aldehydes and ketones. These tests are Dichromate test‚ Tollens test‚ Lucas test‚ DNPH test and Iodoform test. Three samples got positive result in dichromate test and one in Tollens test. Lucas test got one sample that has
Premium Alcohol Oxygen Aldehyde
1.1 CHEMISTRY 2213a ORGANIC CHEMISTRY FOR THE LIFE SCIENCES - organic chemistry is the study of life at the molecular level; to many it is the key to understanding life “The language of chemistry- an international language‚ a language without dialects‚ a language for all of time‚ and a language that explains where we came from‚ what we are‚ and where the physical world will allow us to go” (Nobelist Arthur Kornberg‚ a biochemist‚ 2000) - but its study has been challenging for students for
Free Atom Chemical bond Electron configuration
SYLLABUS Cambridge O Level Chemistry 5070 For examination in June and November 2014 University of Cambridge International Examinations retains the copyright on all its publications. Registered Centres are permitted to copy material from this booklet for their own internal use. However‚ we cannot give permission to Centres to photocopy any material that is acknowledged to a third party even for internal use within a Centre. © University of Cambridge International Examinations 2011 Contents
Premium Chemistry Oxygen Ionic bond
Year 12 Chemistry 2011 Student Handbook Table of Contents Errors 2 Significant Figures 2 States of Matter in Equations 2 Revision Hints 3 Equations 4 VCAA 2008-2011 Key Skills 6 Unit 3 VCAA Study Design 7 Unit 3 Timetable 8 Unit 3 Work Set Questions 10 Unit 4 VCAA Study Design 11 Unit 4 Timetable 12 Unit 4 Work Set Questions 14 ERRORS When instruments are manufactured‚ there is a specified uncertainty within which the instrument is designed
Premium Chemical reaction Titration Analytical chemistry
| |Structure and Preparation of Alkenes. | |Elimination Reactions | Summary Alkenes contain the C=C functional group which can be prepared by 1‚2-elimination reactions such as: • dehydration of alcohols (- H2O) or • dehydrohalogenation of alkyl halides (- HX). Zaitsev’s rule indicates that the preferred product is the more highly substituted‚ and therefore more stable alkene. But the rule is not always obeyed
Premium Alkene Organic reaction Alcohol
The saturated unbranched alkenes will have a much quicker reaction rate but have low enthalpy values as it doesn’t take that much energy to break those bonds. Due to the neo-pentane having the larger density out of the other two isomers of pentane‚ it will have the lowest enthalpy
Premium Statistics Regression analysis Temperature
OH Amino Amines Amides R – N – H \ H R – C=O \NH2 Sulfhydryl Thiols R – SH Phosphate Organic phosphates (double bond between O and P) O R – O – P – O O Alkanes (single carbon bonds) R – C – C – H Alkenes (double carbon bonds) R – C = C – H Alkynes (triple carbon bonds) R – C = C - H Ester linkage (double bond between O and C) O R – C – O – R Ether linkage R – O – R Biochemical Molecules (Macromolecules)
Free Protein DNA Cell
Experiment 11: Synthesis of Dibenzalacetone by the Aldol condensation Introduction: The Aldol condensation reaction‚ under basic conditions‚ involves the nucleophilic addition of an enolate ion to another carbonyl group. The resulting product‚ a beta-hydroxy ketone or aldehyde‚ is called an aldol because it contains both and aldehyde group and the hydroxy group of alcohol. Condensations‚ including aldol condensation‚ combine two or more molecules‚ typically with a loss of a smaller molecule (including
Premium Aldehyde Chemistry Carbonyl