Edible DNA - iGEM 2013
... the two strands are separated by breaking the hydrogen bonds between the base pairs. Next, two new strands are made by reading each side of the DNA ladder, one step (base) at a time. At each step, the matching base fills in (with its associated sugar and phosphate) to complete the rung and lengthen ...
... the two strands are separated by breaking the hydrogen bonds between the base pairs. Next, two new strands are made by reading each side of the DNA ladder, one step (base) at a time. At each step, the matching base fills in (with its associated sugar and phosphate) to complete the rung and lengthen ...
180-183
... Bacterial Viruses A bacteriophage is a kind of virus that infects bacteria. When a bacteriophage enters a bacterium, it attaches to the surface of the bacterial cell and injects its genetic material into it. In 1952, Alfred Hershey and Martha Chase used radioactive tracers to label proteins and DNA ...
... Bacterial Viruses A bacteriophage is a kind of virus that infects bacteria. When a bacteriophage enters a bacterium, it attaches to the surface of the bacterial cell and injects its genetic material into it. In 1952, Alfred Hershey and Martha Chase used radioactive tracers to label proteins and DNA ...
Lecture 4, Exam III Worksheet Answers
... have to be involved in this process? Thymine dimers within DNA. Two thymines beside each other are bonded together by a covalent bond. Nuclease. It is an enzyme that cleaves nucleic acids. Other enzymes that may be needed in this process are the enzymes needed to create DNA and link it together: pri ...
... have to be involved in this process? Thymine dimers within DNA. Two thymines beside each other are bonded together by a covalent bond. Nuclease. It is an enzyme that cleaves nucleic acids. Other enzymes that may be needed in this process are the enzymes needed to create DNA and link it together: pri ...
Modeling DNA Structure and Function
... Build an mRNA molecule that is complementary to one of the DNA strands -- the so called template strand. That is, show your instructor what would happen if the DNA was being transcribed. ...
... Build an mRNA molecule that is complementary to one of the DNA strands -- the so called template strand. That is, show your instructor what would happen if the DNA was being transcribed. ...
Maurice Wilkins
Maurice Hugh Frederick Wilkins CBE FRS (15 December 1916 – 5 October 2004) was a New Zealand-born English physicist and molecular biologist, and Nobel Laureate whose research contributed to the scientific understanding of phosphorescence, isotope separation, optical microscopy and X-ray diffraction, and to the development of radar. He is best known for his work at King's College, London on the structure of DNA which falls into three distinct phases. The first was in 1948–50 where his initial studies produced the first clear X-ray images of DNA which he presented at a conference in Naples in 1951 attended by James Watson. During the second phase of work (1951–52) he produced clear ""B form"" ""X"" shaped images from squid sperm which he sent to James Watson and Francis Crick causing Watson to write ""Wilkins... has obtained extremely excellent X-ray diffraction photographs""[of DNA]. Throughout this period Wilkins was consistent in his belief that DNA was helical even when Rosalind Franklin expressed strong views to the contrary.In 1953 Franklin instructed Raymond Gosling to give Wilkins, without condition, a high quality image of ""B"" form DNA which she had unexpectedly produced months earlier but had “put it aside” to concentrate on other work. Wilkins, having checked that he was free to personally use the photograph to confirm his earlier results, showed it to Watson without the consent of Rosalind Franklin. This image, along with the knowledge that Linus Pauling had published an incorrect structure of DNA, “mobilised” Watson to restart model building efforts with Crick. Important contributions and data from Wilkins, Franklin (obtained via Max Perutz) and colleagues in Cambridge enabled Watson and Crick to propose a double-helix model for DNA. The third and longest phase of Wilkins' work on DNA took place from 1953 onwards. Here Wilkins led a major project at King's College, London, to test, verify and make significant corrections to the DNA model proposed by Watson and Crick and to study the structure of RNA. Wilkins, Crick and Watson were awarded the 1962 Nobel Prize for Physiology or Medicine, ""for their discoveries concerning the molecular structure of nucleic acids and its significance for information transfer in living material.""