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81.
82.
Physical and genetic mapping of the Rhodobacter sphaeroides 2.4.1 genome: presence of two unique circular chromosomes. 总被引:44,自引:30,他引:14 下载免费PDF全文
A macrorestriction map representing the complete physical map of the Rhodobacter sphaeroides 2.4.1 chromosomes has been constructed by ordering the chromosomal DNA fragments from total genomic DNA digested with the restriction endonucleases AseI, SpeI, DraI, and SnaBI. Junction fragments and multiple restriction endonuclease digestions of the chromosomal DNAs derived from wild-type and various mutant strains, in conjunction with Southern hybridization analysis, have been used to order all of the chromosomal DNA fragments. Our results indicate that R. sphaeroides 2.4.1 carries two different circular chromosomes of 3,046 +/- 95 and 914 +/- 17 kilobases (kb). Both chromosome I (3,046 kb) and chromosome II (914 kb) contain rRNA cistrons. It appears that only a single copy of the rRNA genes is contained on chromosome I (rrnA) and that two copies are present on chromosome II (rrnB, rrnC). Additionally, genes for glyceraldehyde 3-phosphate dehydrogenase (gapB) and delta-aminolevulinic acid synthase (hemT) are found on chromosome II. In each instance, there appears to be a second copy of each of these genes on chromosome I, but the extent of the DNA homology is very low. Genes giving rise to enzymes involved in CO2 fixation and linked to the gene encoding the form I enzyme (i.e., the form I region) are on chromosome I, whereas those genes representing the form II region are on chromosome II. The complete physical and partial genetic maps for each chromosome are presented. 相似文献
83.
84.
A K Shiemke W A Kaplan C L Hamilton J A Shelnutt R A Scott 《The Journal of biological chemistry》1989,264(13):7276-7284
Binding of axial ligands to the nickel(II) of isolated factor F430 from the methyl reductase enzyme of Methanobacterium thermoautotrophicum is demonstrated. Evidence of bis-ligand coordination is obtained from the x-ray absorption, optical, and resonance Raman spectral characterization of F430 and its 12,13-diepimeric isomer in the presence of a large excess of cyanide, pyridine, or 1-methylimidazole. Significant broadening and 5-10-nm red shifts of the main 430-nm optical absorption band and shifts of up to 30 cm-1 for the high-frequency Raman lines are observed upon coordination of these axial ligands. The Raman spectra of native F430 and the diepimer with a particular axial ligand are nearly identical. Nickel x-ray absorption edge spectra of the diepimer in the absence and presence of these exogenous ligands are indicative of conversion from a square-planar to a tetragonally distorted octahedral geometry. Analyses of the nickel extended x-ray absorption fine structure data for the ligated diepimer complexes yield detailed structural information for these complexes. Implications of these data with respect to the enzymatic mechanism and the structure of the enzyme-bound factor are discussed. 相似文献
85.
The immune response and the eye. III. Anterior chamber-associated immune deviation can be adoptively transferred by serum 总被引:2,自引:0,他引:2
T A Ferguson J D Hayashi H J Kaplan 《Journal of immunology (Baltimore, Md. : 1950)》1989,143(3):821-826
After the anterior chamber (AC) injection of trinitrophenol-coupled (TNP) spleen cells, it is observed that systemic delayed-type hypersensitivity responses to TNP are inhibited by Ag-specific suppressor T cells. We recently reported that suppression is initiated by viable TNP-coupled T cells within the inoculum and upon further analysis we found that these cells have the surface phenotype of CD4+ Ts inducer cells. We report here that treatment of these TNP-T cells with cycloheximide or cytochalasin-B before to AC injection abolishes suppression, whereas treatment with 2000 rad radiation does not. This indicates that protein synthesis and secretion are required to initiate suppression but proliferation is not. Further, we demonstrate the adoptive transfer of suppression by serum of AC inoculated animals. Detection of the component in serum in adoptive transfer assays, however, requires removal of the spleen before AC injection. We establish that the material in serum is a Ts cell product (T suppressor-inducer factor) based on three criteria: it is Ag specific, genetically restricted, and reactive with a mAb that specifically identifies these molecules. These results suggest that the signal leaving the eye to induce suppression of delayed-type hypersensitivity is T cell derived and that molecules mediating immune regulation for this organ are made within the eye and transported via the serum to the spleen. 相似文献
86.
Mutation analysis of the cystic fibrosis transmembrane regulator gene in native American populations of the southwest 下载免费PDF全文
Theresa A. Grebe Winifred W. Doane Sarah F. Richter Carol Clericuzio R. A. Norman William K. Seltzer Susan N. Rhodes Bruce E. Goldberg Lucy S. Hernried Melody McClure Gail Kaplan 《American journal of human genetics》1992,51(4):736-740
We report DNA and clinical analyses of cystic fibrosis (CF) in two previously unstudied, genetically isolated populations: Pueblo and Navajo Native Americans. Direct mutation analysis of six mutations of the CFTR gene--namely, delta F508, G542X, G551D, R553X, N1303K, and W1282X--was performed on PCR-amplified genomic DNA extracted from blood samples. Haplotype analyses with marker/enzyme pairs XV2c/TaqI and KM19/PstI were performed as well. Of the 12 affected individuals studied, no delta F508 mutation was detected; only one G542X mutation was found. None of the other mutations was detected. All affected individuals have either an AA, AC, or CC haplotype, except for the one carrying the G542X mutation, who has the haplotype AB. Clinically, six of the affected individuals examined exhibit growth deficiency, and five (all from the Zuni Pueblo) have a severe CF phenotype. Four of the six Zunis with CF are also microcephalic, a finding not previously noted in CF patients. Our DNA data have serious implications for risk assessment of CF carrier status for these people. 相似文献
87.
The determination of the rate of release of Ca2+ by pulsed photolysis of the photolabile chelator DM-nitrophen is important for its use in time-resolved physiological studies: the rate of substrate or effector release should be faster than the processes they initiate. Flash photolysis of DM-nitrophen using a 50-ns pulse from a frequency-doubled ruby laser (with emission at 347 nm having energy of ca. 10-20 mJ) yields short-lived photochromic or aci-nitro intermediates. At pH 6.9, double-exponential decay of a photochromic intermediate was observed for DM-nitrophen itself and its Ca2+ complex (tau 1/2 values of 24 and 570 microseconds, and 32 and 220 microseconds respectively), while only monoexponential decay of the DM-nitrophen-Mg2+ complex was detected (tau 1/2 = 31 microseconds). Only the photochemistry of DM-nitrophen-Ca2+ was found to be pH sensitive (monoexponential decay, tau 1/2 approximately 115 microseconds at pH 7.9 and 8.9). Use of the Ca(2+)-sensitive metallochromic dye antipyrylazo III in conjunction with pulsed photolysis of DM-nitrophen-Ca2+ enabled an upper limit of the half-time of release of Ca2+ to be established of ca. 180 microseconds (the rate of association of Ca2+ with the dye was probably rate determining). The rate of Ca2+ photorelease may, however, be faster than this. Thus, the DM-nitrophen-Ca2+ complex releases Ca2+ on photolysis sufficiently rapidly for the study of many Ca(2+)-dependent physiological processes with improved kinetic resolution over conventional mixing methods. 相似文献
88.
Identification and purification of a family of dimeric major cold shock protein homologs from the psychrotrophic Bacillus cereus WSBC 10201. 总被引:2,自引:1,他引:1 下载免费PDF全文
Whole-cell protein patterns of a psychrotrophic Bacillus cereus strain from cultures grown at 7 and 30 degrees C were compared. This analysis revealed that at least three major proteins are expressed at a significantly higher rate at 7 degrees C than at 30 degrees C. The most abundant of these cold-induced proteins was a small polypeptide of 7.5 kDa, designated CspA, of B. cereus. In addition, four small proteins very similar in size to CspA were seen on both 7 degrees C and 30 degrees C two-dimensional protein gels. Immunoblot analysis using B. cereus anti-CspA antibodies indicated that the five proteins described above plus an additional sixth protein not visible on silver-stained two-dimensional gels are members of a B. cereus cold shock protein family. This hypothesis was corroborated by cloning and sequencing of the genes encoding five proteins of this family. The protein sequences deduced are highly similar and show homology to small procaryotic cold shock proteins and to the cold shock domain of eucaryotic Y-box proteins. Besides CspA, only one of the additional five CspA homologs was slightly cold inducible. In the presence of 100 mM NaCl, the two purified members of the protein family (CspA and CspE) elute as dimers at an apparent molecular mass of 15 kDa from a gel filtration column. At higher salt concentrations, they dissociate into their monomers. Their ability to bind to the ATTGG motif of single-stranded oligonucleotides was demonstrated by band shift analysis. 相似文献
89.
The Myxococcus xanthus rfbABC operon encodes an ATP-binding cassette transporter homolog required for O-antigen biosynthesis and multicellular development. 总被引:4,自引:2,他引:2 下载免费PDF全文
A wild-type sasA locus is critical for Myxococcus xanthus multicellular development. Mutations in the sasA locus cause defective fruiting body formation, reduce sporulation, and restore developmental expression of the early A-signal-dependent gene 4521 in the absence of A signal. The wild-type sasA locus has been located on a 14-kb cloned fragment of the M. xanthus chromosome. The nucleotide sequence of a 7-kb region containing the complete sasA locus was determined. Three open reading frames encoded by the genes, designated rfbA, B and C were identified. The deduced amino acid sequences of rfbA and rfbB show identity to the integral membrane domains and ATPase domains, respectively, of the ATP-binding cassette (ABC) transporter family. The highest identities are to a set of predicted ABC transporters required for the biosynthesis of lipopolysaccharide O-antigen in certain gram-negative bacteria. The rfbC gene encodes a predicted protein of 1,276 amino acids. This predicted protein contains a region of 358 amino acids that is 33.8% identical to the Yersinia enterocolitica O3 rfbH gene product, which is also required for O-antigen biosynthesis. Immunoblot analysis revealed that the sasA1 mutant, which was found to encode a nonsense codon in the beginning of rfbA, produced less O-antigen than sasA+ strains. These data indicate that the sasA locus is required for the biosynthesis of O-antigen and, when mutated, results in A-signal-independent expression of 4521. 相似文献
90.
Hillard S. Kaplan Jane B. Lancaster Sara E. Johnson John A. Bock 《Human nature (Hawthorne, N.Y.)》1995,6(4):325-360
Our objective is to test an optimality model of human fertility that specifies the behavioral requirements for fitness maximization
in order (a) to determine whether current behavior does maximize fitness and, if not, (b) to use the specific nature of the behavioral deviations from fitness maximization towards the development of models of evolved
proximate mechanisms that may have maximized fitness in the past but lead to deviations under present conditions. To test
the model we use data from a representative sample of 7,107 men living in Albuquerque, New Mexico, between 1990 and 1993.
The model we test proposes that low fertility in modern settings maximizes number of grandchildren as a result of a trade-off
between parental fertility and next generation fertility. Results do not show the optimization, although the data do reveal
a trade-off between parental fertility and offspring education and income.
We propose that two characteristics of modern economies have led to a period of sustained fertility reduction and to a corresponding
lack of association between income and fertility. The first is the direct link between costs of investment and wage rates
due to the forces of supply and demand for labor in competitive economies. The second is the increasing emphasis on cumulative
knowledge, skills, and technologies in the production of resources. Together they produce historically novel conditions. These
two features of modern economies may interact with evolved psychological and physiological mechanisms governing fertility
and parental investment to produce behavior that maximizes the economic productivity of lineages at the expense of fitness.
If cognitive processes evolved to track diminishing returns to parental investment and if physiological processes evolved
to regulate fertility in response to nutritional state and patterns of breast feeding, we might expect non-adaptive responses
when returns from parental investment do not diminish until extremely high levels are reached. With high economic payoffs
from parental investment, people have begun to exercise cognitive regulation of fertility through contraception and family
planning practices. Those cognitive processes maynot have evolved to handle fitness trade-offs between fertility and parental investment.
A preliminary presentation of this data was published in R. I. M. Dunbar, ed.,Human Reproduction Decisions: Biological and Social Perspectives. New York: St. Martin’s Press, 1995. Support for the research project, “Male Fertility and Parenting in New Mexico,” began
with two seed grants from the University of New Mexico’s Biomedical Research Grants Program, 1988 and 1989, and one from the
University of New Mexico Research Allocations Committee, 1988. Further seed money as well as interim funding came from the
William T. Grant Foundation (#89130589 and #91130501). The major support for the project came from the National Science Foundation
from 1990 to 1993 (#BNS-9011723 and #DBS-911552). Both National Science Foundation grants included Research Experience for
Undergraduates supplements.
Hillard S. Kaplan is an Associate Professor of Anthropology at the University of New Mexico. His earlier research and publications
focused on food sharing, time allocation, parental investment, and reproductive strategies among Ache hunter-gatherers in
Paraguay, Machiguenga and Piro forager-horticulturalists in Peru, and villagers of several ethnicities in Botswana. New research
and theory concern fertility, parental investment, and mating strategies in developed and developing nations. This research
formulates a new theory of reproductive decision-making and the demographic transition, integrating human capital and parental
investment theory in a synthesis of economic and evolutionary approaches.
Jane B. Lancaster is a Professor of Anthropology at the University of New Mexico. Her research and publications are on human
reproductive biology and behavior, especially human parental investment; women’s reproductive biology of pregnancy, lactation,
and child-spacing; and male fertility and investment in children. Current research with Hillard S. Kaplan is on male life
history strategies among a large sample of men in New Mexico. She has coedited three books on human parental investment:School-Age Pregnancy and Parenthood (with B. Hamburg),Parenting across the Life Span (with J. Altmann, A. Rossi, and L. Sherrod), andOffspring Abuse and Neglect (with R. Gelles). She is scientific editor of a quarterly journal,Human Nature: An Interdisciplinary, Biosocial Perspective published by Aldine de Gruyter. She is also a council member of the newly formed Human Behavior and Evolution Society.
John A. Bock is Andrew W. Mellon Post-Doctoral Fellow in Epidemiology and Population Health at the National Centre for Epidemiology
and Population Health, The Australian National University. His research focuses on the allocation of parental investment and
the determinants of children’s activities, integrating aspects of economic and evolutionary theory. He has ongoing field research
with Bantu and Bushmen agro-pastoralists and forager-horticulturalists in the Okavango Delta, Botswana. He is also collaborating
with Lancaster and Kaplan on the determinants of progeny distribution and homosexuality among New Mexican men.
Sara E. Johnson is a Ph.D. candidate at the University of New Mexico. Her major research trajectory focuses on trade-offs
in life history characters. Her research experience includes participation in a study of variation in growth and development
among children in a multi-ethnic community in the Okavango Delta, Botswana, in addition to her dissertation work on individual
variation in growth and mortality among juvenile baboons. She is collaborating with Lancaster and Kaplan on the association
between survival and fertility among Albuquerque men. 相似文献