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221.
Enzymes, such as urease and uricase, were entrapped in three kinds of hollow fibers. The apparent Michaelis–Menten constants Km(app) obtained for these enzyme reactors were always larger than Km of free enzyme because of the permeation resistance of substrate across the hollow-fiber membrane. Km(app) increased with increasing degree of permeation resistance across the membrane by the increase in enzyme concentration. The half-life of the entrapped urease in the continuous reaction system was 60–80% of that of free enzyme. Activation energies of hollow-fiber enzyme reactors were always smaller than that of the free enzyme, because the activation energy of permeation was smaller than that of the enzyme reaction.  相似文献   
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We compared the susceptibility of five herbivores to tomato resistance induced by methyl jasmonate (MeJA) treatment. We tested for lethal effects against five herbivores (Spodoptera litura, Mamestra brassicae, Frankliniella occidentalis, Tetranychus urticae, and Henosepilachna vigintioctopunctata) at various MeJA concentrations. The mortality of all five herbivores increased significantly with increasing MeJA concentration. The 25 % lethal concentration was 0.03 μM for both first-instar larvae of S. litura and third-instar larvae of M. brassicae, 0.51 μM for third-instar larvae of S. litura, 0.76 μM for adult T. urticae, 2.4 μM for first-instar larvae of F. occidentalis, and 5.7 μM for first-instar larvae of H. vigintioctopunctata. Thus, the degree of susceptibility to MeJA-induced resistance of tomato was first-instar larvae of S. litura = third-instar larvae of M. brassicae > third-instar larvae of S. litura ≈ adult T. urticae > first-instar larvae of F. occidentalis > first-instar larvae of H. vigintioctopunctata. Mortality of first-instar larvae of M. brassicae was >90 % at all concentrations. Mortality of fourth-instar larvae of H. vigintioctopunctata (<7 %) was similar to that of the control at all MeJA concentrations. We also detected statistically significant weight loss of the surviving lepidopteran larvae, increased larval duration of F. occidentalis and H. vigintioctopunctata, and reduced egg production by T. urticae grown on MeJA-treated tomato, suggesting that the MeJA-induced resistance can control these herbivores, but effectiveness is different on different species and growth stage. Feeding by both M. brassicae and H. vigintioctopunctata larvae activated JA-inducible genes in tomato.  相似文献   
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The age of tissues and cells can be accurately estimated by DNA methylation analysis. The multitissue DNA methylation (DNAm) age predictor combines the DNAm levels of 353 CpG dinucleotides to arrive at an age estimate referred to as DNAm age. Recent studies based on short‐term observations showed that the DNAm age of reconstituted blood following allogeneic hematopoietic stem cell transplantation (HSCT) reflects the age of the donor. However, it is not known whether the DNAm age of donor blood remains independent of the recipient's age over the long term. Importantly, long‐term studies including child recipients have the potential to clearly reveal whether DNAm age is cell‐intrinsic or whether it is modulated by extracellular cues in vivo. Here, we address this question by analyzing blood methylation data from HSCT donor and recipient pairs who greatly differed in chronological age (age differences between 1 and 49 years). We found that the DNAm age of the reconstituted blood was not influenced by the recipient's age, even 17 years after HSCT, in individuals without relapse of their hematologic disorder. However, the DNAm age of recipients with relapse of leukemia was unstable. These data are consistent with our previous findings concerning the abnormal DNAm age of cancer cells, and it can potentially be exploited to monitor the health of HSCT recipients. Our data demonstrate that transplanted human hematopoietic stem cells have an intrinsic DNAm age that is unaffected by the environment in a recipient of a different age.  相似文献   
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Biochemical and genetic studies on the arginine-requiring auxotrophs derived from a Serratia marcescens strain were carried out. The arg mutants were classified into seven biochemical groups based on their growth response to five precursors of arginine biosynthesis and enzyme deficiency. Reciprocal transduction tests among those arg mutants divided them into three linkage groups, and the fine mapping in each of the groups by two- or three-point crosses revealed the following arrangement of loci. (1) arg44–thy11–lys1; (2) met1–glt2–argE–(arg19–arg51)–arg120–argG–argH; (3) arg33–pyr4. Five of the seven biochemically distinct arg mutants belonged to the second linkage group, and they constituted an arg-gene cluster. A characteristic feature of the arg-gene cluster of S. marcescens is that it involves argG, which was previously reported only in the Proteus group of Enterobacteriaceae.  相似文献   
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