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961.
A. E. Clarke M. A. Anderson A. Atkinson A. Bacic P. R. Ebert W. Jahnen W. M. Lush S. -L. Mau J. R. Woodward 《Plant molecular biology》1989,13(3):267-271
A summary of recent work on molecular aspects of self-incompatibility in Nicotiana alata is presented. The amino acid sequences of style proteins corresponding to different S-alleles of N. alata have a high level of homology in some regions and are variable in other regions. The regions of homology include N-terminal sequences as well as most of the glycosylation sites and cysteine residues. The glycosyl substituents may consist of a number of glycoforms. The isolated style S-glycoproteins inhibit in vitro growth of pollen tubes. The S-glycoproteins tested inhibited the growth of pollen of several S-genotypes, and there was some specificity in the interaction. Heat treatment of the isolated S-glycoproteins dramatically increased their activity as inhibitors of pollen tube growth, although the specificity in the interaction was lost. The nature of the S-allele products in pollen is not yet established. 相似文献
962.
Nicola J. Atkinson Brian V. Ford-Lloyd H. John Newbury 《Plant Cell, Tissue and Organ Culture》1989,17(1):59-70
Somaclone production in Antirrhinum majus plants by regeneration of plants from callus cultures has been achieved using three types of explant tissue. Regeneration from mature stem internode-derived callus was extremely poor. Callus derived from seedling shoot tips could be induced to form new shoots in six of seven cultivars tested. Regeneration was achieved in all seven cultivars when callus was produced from segments of hypocotyl and was most effective using agar-solidified medium containing 0.25 mgl-1 naphthoxyacetic acid + 10% coconut milk. In this case, five of the cultivars produced shoots directly, one produced leaves from the petioles of which new shoots emerged, and one regenerated plants chiefly through the production of embryoids. 相似文献
963.
Angus Atkinson 《Polar Biology》1989,9(6):353-363
Summary An intensive net sampling survey was conducted around the island of South Georgia during November/December 1981. The distribution and copepodite stage structure of the dominant copepods Calanoides acutus, Calanus simillimus, C. propinquus, Rhincalanus gigas, Metridia lucens and Metridia gerlachei were compared. The herbivorous species had completed their spring vertical migration and their summer generations were developing during the survey. At every station, Calanoides acutus was noticeably more advanced than Rhincalanus gigas in its reproductive cycle. The species were also more advanced in their development in the SE oceanic part of the survey area than in the NW. However, copepod development rates are rapid at this time of year, and this apparent regional difference may be due mainly to temporal variation during the four weeks of the survey. A truly regional variation in timing of reproduction was found when development was compared between shelf and oceanic waters. Spawning of Rhincalanus gigas and particularly of Calanoides acutus was later over the shelf. The age structure of the epi-mesopelagic metridinids also differed between shelf and oceanic waters, but no age differences were found for either Calanus simillimus or C. propinquus, both of which live and spawn higher in the water column than the other species. The presence of the South Georgia shelf also limited the overall abundance of the two deeper living metridinids. However, the length of time between spawning (and production of large numbers of early copepodids) and sampling had the largest influence on observed species abundance within the survey area. 相似文献
964.
David J. Nicholls Trichur K. Sundaram Tony Atkinson Nigel P. Minton 《FEMS microbiology letters》1990,70(1):7-13
A 3 kb DNA fragment containing the gene (mdh) encoding malate dehydrogenase (MDH) from the thermophile Thermus aquaticus B was cloned in Escherichia coli and its nucleotide sequence determined. Comparative analysis showed the nucleotide sequence to be very closely related to that determined for the Thermus flavus mdh gene and flanking regions, with no differences between the predicted amino acid sequences of the MDHs. A proximal open reading frame, identified as the sucD gene, and the mdh gene may be parts of the same operon in T. aquaticus B. Expression of the T. aquaticus B mdh gene in E. coli was found to be at a relatively low level. A simple method for purification of thermostable MDH from the E. coli clone containing the T. aquaticus B mdh gene is presented. 相似文献
965.
Lewis M. Brown Irene Gargantini D. James Brown Harvey J. Atkinson J. Govindarajan Gregory C. Vanlerberghe 《Journal of applied phycology》1989,1(3):211-225
A largely unexplored area is the application of digital image processing to counting and sizing of microalgal cells from culture.
Commercial systems are available, but have not been tested, nor necessarily optimized for high speed counting and sizing of
phytoplankton. The present work describes the design, construction, specifications and comparative performance of an inexpensive
system optimized for counting and sizing microalgal cells. This system has been tested with cells of the picoplankton to nanoplankton
size ranges (1–20 μm). The hardware was a widely available standard microcomputer, an inexpensive video camera and monitor,
and a video digitization board (frame grabber). A modifiable menu-driven program (PHYCOUNT) was written and provisions made
to make this program available to other workers. The program is constructed such that it can be adapted to a variety of hardware
setups Video digitization boards). Comparison of growth curves for microagae revealed there were no significant differences
in division rate and cell yield as assessed by the image analysis method compared to manual counts with a hemacytometer. Several
hundred cells were counted routinely within 10–15 s, far exceeding the counting rate achieved by hand tally. A variable transect
feature allowed sampling every nth pixel and provided a substantial increase in execution speed. More than 1000 counts can
be done per day. A protocol for the use of 96-well plates of polyvinyl chloride as counting chambers contributed to the processing
of large numbers of samples rapidly. Other routines developed provided subtended area, defined the coordinates of cell perimeter,
and derived cell length and width. The calculation of the latter two parameters was usually done off-line as data output is
in standard numerical form accessible by other programs. Experience with daily use of the PHYCOUNT program and imaging hardware
reveal that the system is reliable for cell counting and sizing. The presence of bacteria in the algal cultures does not affect
cell counting or sizing. 相似文献
966.
Previously, Man8-14GlcNAc oligosaccharides were isolated from highly purified Saccharomyces cerevisiae invertase and shown by one-dimensional 1H NMR spectroscopy and alpha 1,2-linkage-specific mannosidase digestion to constitute a homologous series of nearly homogeneous compounds, which appeared to define the intermediates in oligosaccharide core synthesis in yeast (Trimble, R.B. and Atkinson, P.H. (1986) J. Biol. Chem., 261, 9815-9824). To evaluate whether invertase oligosaccharides reflected global core processing of yeast glycans, the soluble glycoprotein pool of disrupted log-phase cells was digested with endo-beta-N-acetyl-glucosaminidase H and Man8-13GlcNAc were isolated by Bio-Gel P-4 chromatography. Although analysis of each size class by one-dimensional 400 MHz and two-dimensional 500 MHz phase-sensitive COSY 1H NMR spectroscopy revealed considerable structural heterogeneity in all but Man8GlcNAc, the major positional isomer in Man9-13GlcNAc (approximately 50%) was identical to that previously elucidated on invertase. The heterogeneity resided in four families of oligosaccharides: (i) Glc3Man9GlcNAc----Man8 GlcNAc trimming intermediates; (ii) alpha-mannosidase degradation products of the principal isomers; (iii) mannan elongation intermediates; (iv) core structures with the alpha 1,2-linked mannose usually removed by the processing alpha-mannosidase. The potential for the vacuolar alpha-mannosidase (AMS1 gene product) to generate heterogeneity in vitro was confirmed by isolating oligosaccharides from AMS1 and ams1 yeast strains in the presence of a Man13GlcNAc[3H]-ol marker (where GlcNAc[3H]-ol is N-acetylglucosamin [1-3H]itol). Degradation of the Man13GlcNAc[3H]-ol to Man9-12GlcNAc[3H]-ol occurred in the former, but not in the latter. A role for the vacuolar alpha-mannosidase in generating at least some heterogeneity in vivo was inferred from the 1H NMR spectrum of the AMS1 Man11GlcNAc pool, which showed more structural isomerism than seen in the spectrum of a comparable ams1 Man11GlcNAc preparation. Thus, the principal biosynthetic pathway of inner core mannan in Saccharomyces is defined by the Man8-13GlcNAc oligosaccharides found on external invertase, while structural heterogeneity in these size classes results from precursor processing in the endoplasmic reticulum, core extension in the Golgi and metabolic degradation in the vacuole. 相似文献
967.
During both spontaneous and thyroid hormone (TH)-induced metamorphosis, the Rana catesbeiana tadpole undergoes postembryonic developmental changes in its liver which are necessary for its transition from an ammonotelic larva to a ureotelic adult. Although this transition ultimately results from marked increases in the activities and/or de novo synthesis of the urea cycle enzymes, the precise molecular means by which TH exerts this tissue-specific response are presently unknown. Recent reports, using RNA from whole Xenopus laevis tadpole homogenates and indirect means of measuring TH receptor (TR) mRNAs, suggest a correlation between the up-regulation of TRβ-mRNAs and the general morphological changes occurring during amphibian metamorphosis. To assess whether or not this same relationship exists in a TH-responsive tissue, such as liver, we isolated and characterized a cDNA clone containing the complete nucleotide sequence for a R. catesbeiana urea cycle enzyme, ornithine transcarbamylase (OTC), as well as a genomic clone containing a portion of the hormone-binding domain of a R. catesbeiana TRβ gene. Through use of these homologous sequences and a heterologous cDNA fragment encoding rat carbamyl phosphate synthetase (CPS), we directly determined the relative levels of the TRβ, OTC, and CPS mRNAs in liver from spontaneous and TH-induced tadpoles. Our results establish that TH affects an up-regulation of mRNAs for its own receptor prior to up-regulating CPS and OTC mRNAs. Moreover, results with cultured tadpole liver demonstrate that TH, in the absence of any other hormonal influence, can affect an up-regulation of both the TRβ and OTC mRNAs. © 1992 Wiley-Liss, Inc. 相似文献
968.
K F Adams S M McAllister H el-Ashmawy S Atkinson G Koch D S Sheps 《Journal of applied physiology》1992,73(5):2097-2104
To better characterize the relationship between left ventricular volume response and improved ventricular ejection and output during supine exercise in normal subjects, 36 healthy asymptomatic volunteers (age 39 +/- 17 yr) were studied with radionuclide ventriculography during recumbent bicycle ergometry. Relative changes in left ventricular end-diastolic and end-systolic volume were measured at rest and during exercise by a modification of the radionuclide counts-based method that accounted for variability in stress blood pool counts. A biphasic response was noted in left ventricular end-diastolic volume with an initial increase in early exercise (8.5 +/- 11% at 200 kpm/min and 11 +/- 12% at 300 kpm/min) followed by a progressive and significant decline at peak exercise (-3.3 +/- 18% at 547 +/- 140 kpm/min; P < 0.05). There was substantial variation in end-diastolic volume response at peak exercise in the group as a whole, which could be more closely related to changes in end-systolic volume (r = 0.84, P < 0.0001) than in heart rate (r = -0.57, P < 0.01) or age (r = 0.36, P < 0.05) of the study subjects. Despite the decline in ventricular filling, systolic function appeared to improve dramatically at peak exercise (change in left ventricular ejection fraction 15.5 +/- 6.4, P < 0.0001). Although not directly related to increasing systolic ejection, end-diastolic volume was directly related to the percent change in stroke volume at peak exercise among the study subjects (r = 0.88, P < 0.0001).(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
969.
Changes in human muscle protein synthesis after resistance exercise. 总被引:10,自引:0,他引:10
A Chesley J D MacDougall M A Tarnopolsky S A Atkinson K Smith 《Journal of applied physiology》1992,73(4):1383-1388
970.
Parathyroid hormone and prostaglandin E2 stimulate both inositol phosphates and cyclic AMP accumulation in mouse osteoblast cultures.
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R W Farndale J R Sandy S J Atkinson S R Pennington S Meghji M C Meikle 《The Biochemical journal》1988,252(1):263-268
Parathyroid hormone (PTH) and prostaglandin E2 (PGE2) are physiological agonists which stimulate bone cells to resorb bone, a process by which the mineralized extracellular bone matrix is dissolved. Bone resorption has a key role in the maintenance of plasma calcium levels. It has been established that both PTH and PGE2 activate adenylate cyclase in osteoblasts, but it is apparent that (1) the two agents have qualitatively different effects on osteoblasts, and (2) the generation of cyclic AMP cannot account for all the effects of PTH on bone cell metabolism. Others have demonstrated that PTH and PGE2 may also elevate intracellular calcium levels, but the mechanism by which this is achieved has not been fully defined. Here we have investigated the effects of PTH on neonatal mouse osteoblasts in culture and shown that physiological concentrations of the hormone (50 nM) caused a small increase (22%) in total inositol phosphates accumulation, with a larger increase (40%) in inositol trisphosphate. We found that this activation occurred at lower concentration than was necessary to activate adenylate cyclase. PGE2 was a more effective activator of inositol phosphates accumulation than PTH, causing up to 300% increase in the total inositol phosphates after 30 min. Both PTH and PGE2 stimulated cyclic AMP accumulation, but the activation of adenylate cyclase by forskolin did not enhance inositol phosphates production. We conclude that both PTH and PGE2 stimulate phosphoinositide turnover in mouse osteoblasts and suggest that this mechanism may contribute to their elevation of intracellular calcium in bone cells. 相似文献