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Conditions for obtaining stable protoplasts from Sclerotium glucanicum and their reversion to hyphal growth were determined. 1,3-beta-Glucan synthase activity was detected in particulate enzyme fractions from mycelium and protoplasts of Scl. glucanicum. UDP-[U-14C]glucose was linearly incorporated into a beta-glucan for about 20 min at 25 degrees C. Optimum pH and temperature values, as well as thermal stabilities of the 1,3-beta-glucan synthase activity, were determined. High concentrations of EDTA were inhibitory. Enzyme activity was stimulated by ATP and GTP. The apparent Km value for UDP-glucose was 0.54 mM. The reaction product was characterized as 1,3-beta-glucan by 13C NMR spectroscopy and hydrolysis products of an exo-1,3-beta-glucanase. 相似文献
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S P Klinken J W Hartley T N Fredrickson U R Rapp H C Morse rd 《Journal of virology》1989,63(5):2411-2414
The susceptibility to tumors induced by raf and raf/myc retroviruses was investigated in BALB/c, C57BL/6, (BALB/c x C57BL/6)F1 and (BALB/c x C57BL/6) backcross mice. Newborn mice were susceptible to neoplasms generated by both viruses, but resistance to raf-induced leukemia developed rapidly in all mice as they matured. Older C57BL/6 mice were also resistant to raf/myc lymphomas, whereas BALB/c mice remained susceptible to the virus at all ages, indicating that different genes control susceptibility to raf and raf/myc tumors. From these data and the susceptibility of C x B recombinant inbred strains, it appears that very few genes (perhaps even a single gene) may govern susceptibility to raf/myc lymphomas and that resistance is the dominant trait. 相似文献
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raf/myc-infected erythroid cells are restricted in their ability to terminally differentiate. 下载免费PDF全文
A comparison was made of the in vitro erythroid colony-forming abilities of v-raf-, v-myc-, and v-raf/v-myc-containing retroviruses. In methylcellulose, v-raf efficiently produced colonies of well-differentiated hemoglobin-synthesizing erythroid cells, whereas v-raf/v-myc-infected erythroid cells were inhibited from terminally differentiating but retained the ability to replicate extensively. In contrast, v-myc was unable to stimulate the formation of erythroid colonies. 相似文献
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Short-term (15-min-duration) and long-term (5- to 6-day-duration) test procedures have been developed for determining the efficiency of the removal of bacteriophage phi X174 by air-sterilizing filters. These procedures were sensitive enough to measure a 10(8)-fold reduction in the number of bacteriophage. A filter commonly used in industrial air sterilizations (Domnick-Hunter Bio-X borosilicate glass) effected a 10(8)-fold removal of viable phage in both short-term and long-term tests. A prototype low-flux, hollow-fiber membrane gave similar results; however, a prototype high-flux, hollow-fiber membrane removed only about 99.999% of the bacteriophage in short-term tests. 相似文献
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T S Elton C C Stephan G R Taylor M G Kimball M M Martin J N Durand S Oparil 《Biochemical and biophysical research communications》1992,184(2):1067-1073
A rat genomic Southern blot, probed with a type I angiotensin II receptor probe, demonstrated that two highly homologous type I angiotensin II receptors were present. A rat genomic library was subsequently screened and four clones were isolated. From restriction mapping, differential hybridization, polymerase chain reaction amplification and sequence analyses we have determined that there are two unique type I angiotensin II receptor genes. The first of these genes corresponds to the published rat vascular complementary DNA sequence; the second, corresponds to a novel receptor not previously described. 相似文献
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Roelof-Jan Oostra Stephan Kemp Pieter A. Bolhuis Elisabeth M. Sleeker-Wagemakers 《Human genetics》1996,97(4):500-505
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited disorder of the optic nerves. It has been proposed that
the specific mutations in the mitochondrial DNA (mtDNA) that are associated with LHON require and X-chromosomally encoded
permissive factor in order to become expressed. This would explain both the preponderance of male patients and the fact that
most carriers of specific mtDNA mutations remain unaffected. Although linkage studies have been negative so far, the existence
of such a factor has not been ruled out. We investigated the genealogical data of 24 large LHON pedigrees and concluded that
the presumed X-linked factor would be recessively inherited and that at least 57% of the affected females would be heterozygous.
Therefore, these females must be the victim of nonrandom X-chromosomal inactivation (skewed lyonization). However, analysis
of X-chromosomal methylation patterns in 16 LHON-affected females revealed substantial skewing in only 15%–20% of cases, which
is not significantly different from the patterns in 49 controls. Moreover, we found the frequency of LHON in daughters of
affected heterozygous females to be twice to three times as high as in daughters of unaffected heterozygous females, which
cannot be explained by an X-chromosomally inherited factor. We conclude that the results of our investigations do not support
the hypothesis that LHON is a digenic disease with an X-linked factor being the main cause of loss of vision in the presence
of relevant mtDNA mutations.
Received: 1 June 1995 / Revised: 20 September 1995 相似文献
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