Black Holes, Shock Waves, and Causality in the AdS/CFT Correspondence

We find the expectation value of the energy-momentum tensor in the CFT corresponding to a moving black hole in AdS. Boosting the black hole to the speed of light, keeping the total energy fixed, yields a gravitational shock wave in AdS. The analogous procedure on the field theory side leads to ``light cone'' states, i.e., states with energy-momentum tensor localized on the light cone. The correspondence between the gravitational shock wave and these light cone states provides a useful tool for testing causality. We show, in several examples, how the CFT reproduces the causal relations in AdS.Comment: Minor corrections, references adde

Growth inhibition of neurospora by canavanine, and its reversal

Canavanine, an amino acid from jack beans, was discovered by Kitagawa and coworkers in 1929 (1, 2). The substance is not combined in the proteins of the seed, but occurs in the free state, and makes up 2.5 per cent of the dry weight of jack beans (3). In a series of papers available to the authors for the most part in abstract only, the Japanese workers have reported extensive investigations into the chemistry and physiology of the substance. The structure of canavanine was established by Gulland and Morris (4) and by Kitagawa and Takani (5) as NH2•C(:NII)•NII•O•CH2•CH2•CHNH2•COOH. Natural canavanine is of the L configuration (6)

Physiological Aspects of Genetics

A considerable amount of evidence indicates that desoxyribonucleic acid is capable of duplicating itself, a property also possessed by genes. (By a self-duplicating material, we mean one which plays some essential role in its own production.) Watson & Crick (1) have proposed a new structure for desoxyribonucleic acid which not only takes into account the existing analytical and x-ray diffraction data but also seems capable of explaining the mechanism of duplication. Their model consists of two helical chains coiled around the same axis, the purine and pyrimidine bases on the inside, the phosphate groups on the outside. The chains are held together by hydrogen bonds between the bases, the adenine residues of either chain being bonded specifically to thymine in the other, and similarly guanine to cytosine. The sequence of bases along one chain is not restricted, but once fixed the sequence along the other chain is determined. This complementarity, which is the most novel feature of the structure, suggests that duplication takes place by separation of the two chains, followed by the synthesis of its complement alongside each chain. The model is supported by recent x-ray diffraction studies (2, 3)

A microbiological method for the determination of choline by use of a mutant of Neurospora

Previous communications from this laboratory have described the production of biochemical mutants in the mold Neurospora by means of ultraviolet and x-rays (1, 2). Such mutants are characterized by the inability to carry out specific chemical syntheses which normally occur in the unmutated, or wild type, strain. In each case which has been genetically analyzed the failure of the synthesis has been found to be related to the mutation of a single gene. The strain to be described, known as No. 34486, or cholineless, arose from a culture of wild type Neurospora crassa which had been irradiated with ultraviolet light. It was found to be unable to grow in a medium containing only salts, sugar, and biotin, but it grew normally on the addition of a mixture of water-soluble vitamins. When the components of the mixture were tested singly, it was found that the addition of choline alone permitted normal growth. Up to the present, no completely satisfactory method for the determination of choline in natural products and tissue extracts has been described. Chemical methods, such as precipitation of the reineckate, lack specificity, while the biological method of Fletcher, Best, and Solandt (3) is time-consuming and difficult, and “possesses many dangerous pitfalls for the chemist” (4). The whole subject has been critically reviewed by Best and Lucas (4). It was therefore of interest to determine whether the Neurospora mutant is a suitable test organism in a quantitative assay for choline. The experiments to be described show that this is the case and form the basis of a simple, sensitive, and specific method for the determination of choline in natural products. By this procedure it is possible to determine choline in a concentration of 0.02 mg. per liter; routine analyses can be run on 100 mg. samples of material

Methionine synthesis in Neurospora. The isolation of cystathionine

Among artificially produced biochemical mutants of Neurospora, those which have lost the ability to synthesize methionine form the largest class. At the present writing 87 occurrences of the methionineless character have been observed in this laboratory following treatment of wild type spores with high frequency radiations (1) or mustard gas (2). Methionineless mutants differ from wild type Neurospora in that they fail to grow on a medium containing only sugar, inorganic salts, and biotin, but do grow if, in addition to these constituents, methionine is supplied. In many of the mutants failure of methionine synthesis results from a block in the reduction of sulfate, which, except for a trace of biotin, is the sole source of sulfur in the basal medium. These strains can utilize reduced forms of inorganic sulfur for growth, as well as methionine and other organic sulfur compounds. On the other hand, some of the mutants require organically bound sulfur for growth, an indication that in these strains the block in methionine synthesis comes at a later stage than sulfate reduction. Similar classes of methionine-requiring mutants have been reported in the mold Ophiostoma by Fries (3) and in Escherichia coli by Lampen et al. (4-6)

The L-amino acid oxidase of Neurospora

In 1944 one of us described a D-amino acid oxidase in extracts of Neurospora crassa (1). Except for slight activity against L-glutamate, no oxidation of L-amino acids was observed. Recently a means for inducing the formation of a soluble L-amino acid oxidase by the mold was reported by Bender, Krebs, and Horowitz (2). This is accomplished by reducing the biotin content of the basal medium (3) from the 5 γ per liter usually employed to 0.25 γ per liter. When cultured in such a medium, Neurospora produces an active L-amino acid oxidase which can be demonstrated both in extracts and in the medium. Reduction of the biotin level produces no effect on the D-amino acid oxidase, which is still found in extracts but not in the culture medium. The activity of the L-oxidase toward thirty-eight amino acids has been investigated by Bender and Krebs (4). The initial purpose of the present investigation was to explore certain possibilities for a genetic study of the enzyme. Of special interest was the fact, cited by Bender et al. (a), that the oxidase could not be detected in all of the wild type strains tested. The question arose as to whether this is due to the genetic inability of certain strains to form the enzyme. In connection with the investigation of this problem a general survey of the properties of the enzyme was carried out, together with a preliminary study of the mechanism of the biotin effect and of the adaptive formation of the enzyme. The results of these studies are reported below. Simultaneously with our investigation and independently of it, Dr. K. Burton (5), working in Professor Krebs’ laboratory, has carried out a study of the Neurospora L-amino acid oxidase. Where our respective studies overlap mutual confirmation was obtained in most essential points. We wish to thank Dr. Burton for permission to read his manuscript before publication

The Origin of Life

The origin of life is in a sense a genetic problem, for, as H. J. Muller pointed out many years ago, the essential attribute that identifies living matter is its capacity to replicate itself and its variants (1). Because this uniquely biological property has its physical basis in proteins and nucleic acids, the goal of modern work on the origin of life is to discover the manner of origin of these polymers and of the interactions between them that constitute the genetic mechanism. In attempting to review this subject in a limited space, we cannot undertake an exhaustive treatment. Rather, we summarize work published principally since 1970 in the following areas, with emphasis on those aspects that are of greatest current interest: 1. precambrian paleontology, 2. chemical evolution of genetically important monomers, 3. prebiotic dehydration-condensation reactions, 4. organic compounds in meteorites and interstellar space, and 5. biological exploration of the planets. A large number of review articles (2-5), critical and theoretical discussions (6-8), books (9-16), and conference proceedings (17-21) dealing with the origin of have appeared in recent years. In addition, a new serial, the Journal of Molecular Evolution, publishing papers on this and related subjects, appeared in 1971; the journal Space Life Sciences has been renamed "Origins of Life," and a society, the International Society for the Study of the Origin of Life, was recently founded

The d-amino acid oxidase of Neurospora

Among artificially produced mutants of the mold Neurospora have been found strains lacking the ability to synthesize specific amino acids (1, 2). In the course of biochemical and genetic studies of this group of mutants it was observed that some of the mutants, e.g. those deficient in methionine, leucine, and arginine,(1) are able to utilize racemic mixtures of the amino acids with the same efficiency as the l, or physiologically occurring, forms. In the cases of the leucine- and the methionine-requiring mutants it was also possible to show utilization of the ar-keto analogues. It thus appeared possible that the mode of conversion of the d to the l isomers consists in oxidative deammation, followed by resynthesis. A study was therefore undertaken to test the ability of Neurospora to oxidize the “unnatural” optical isomers of the amino acids. It was found that extracts of the mold contain a d-amino acid oxidase similar in its action to the d-amino acid oxidase of mammalian kidney and liver (3). This finding supports the above hypothesis for the conversion of the d- to the l-amino acids. Since it appears that the d-amino acid oxidase has not been previously described in fungi, a number of experiments were performed on the Neurospora enzyme, the results of which are reported here

The ornithine cycle in Neurospora and its genetic control

It has been emphasized by Haldane (1) that for studies of intermediary metabolism "the new science of genetics furnishes a very powerful method." Such a method is founded upon the general premises that genes control many of the chemical reactions within an organism, and that gene mutations by blocking a reaction chain at various points may, in effect, resolve a metabolic process into some of its constituent stages. For instance, the genetics of such diseases as alcaptonuria and cystinuria have elucidated certain problems in human metabolic processes (2), and studies in the genetics of plant pigments have increased the knowledge of of the biochemistry of anthocyanins (3). But the study of metabolism by way of genetic differences in naturally occurring populations is limited not only by the low rate of mutation but also by the lethal character of most mutations of genes controlling vital functions. By increasing the mutation rate of an organism, through irradiation or otherwise, it is possible to create a number of genetic blocks at various steps in the syntheses of substances or in other processes of metabolism. The problem of preserving mutations ordinarily lethal has been met by Beadle and Tatum (4) in a general course of procedure developed around work with the ascomycetous mold Neurospora. The wild type of this organism is able to carry out all the syntheses essential to its normal growth and reproduction if biotin, inorganic salts, and a suitable source of carbon are available. Strains of Neurospora are irradiated with x-ray or ultraviolet rays on the assumption that mutations will be induced in genes controlling the syntheses of such substances as vitamins and amino acids. Mutant strains of this kind cannot grow on merely inorganic salts, sugar, and biotin, "minimal medium," but can be expected to grow if the product of the blocked synthesis is added to the minimal medium. From irradiated Neurospora there has been isolated in this laboratory a series of mutant strains which require for growth the presence of arginine in the culture medium. A study of the specific biochemical characteristics of members of this group of mutants has made it possible to demonstrate in Neurospora crassa an ornithine cycle similar to that proposed by Krebs and Henseleit (5) as occurring in mammalian liver, and to assign various steps in the cycle to the influence of particular single genes. To our knowledge the ornithine cycle has not previously been demonstrated in plants