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831.
Seven paraquat resistant calluses of tobacco (Nicotiana tabacumL. cv. Samsun) were obtained by three successive screeningsof protoplast-derived calluses on a paraquat containing medium.Superoxide dismutase (SOD) activity of the resistant calluseswas 14- to 159-fold that of the leaf cells on protein basis.Paraquat-resistant calluses, however, showed little increasein catalase and peroxidase activities. More than 90% of SODactivity in the resistant calluses was inhibited by KCN, aswas the SOD activity in leaves, indicating that the major SODin the callus appears to be the Cu, Zn containing enzyme. Thecallus cells, however, expressed the immunologically distinguishedSOD isozyme from the enzyme in the leaves. (Received April 23, 1984; Accepted August 6, 1984)  相似文献   
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A new substance (ES-1) which localizes on the ectodermal and espophageal epithelia of sea urchin embryos was identified by a monoclonal antibody, McA ES-1. McA ES-1 recognized a 175 KDa protein of fertilized and 200 KDa in proteins of unfertilized egg-cortices. By indirect fluorescent antibody staining, ES-1 was found on the plasma membrane of fertilized eggs and in the cortical region of unfertilized eggs. ES-1 was not contained in the cortical granules and remained fixed in the cortex after centrifugation of unfertilized eggs for 30 min at 20,000 g. The polarized localization of ES-1 on the apical surface of ectodermal epithelial cells continued to the metamorphosis. It disappeared from mesenchyme cells and other migrating cells of the gastrula, while ES-1 was reexpressed in the presumptive esophagus to be connected with ectodermal epithelium. This may suggest a functional significance of ES-1 in establishment of cell polarity in the epithelium of larvae. In metamorphosing larvae and adults, the apical localization of ES-1 could no longer be found, and it was found in coelomocytes. From these findings, it is concluded that ES-1 was a novel surface substance of embryos and is probably phagocytosed at metamorphosis.  相似文献   
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The effect of the external pH on the intracellular pH in mungbean (Vigna mungo (L.) Hepper) root-tip cells was investigatedwith the 31P nuclear magnetic resonance (NMR) method. The 31PNMR spectra showed three peaks caused by cytoplasmic G-6-P,cytoplasmic Pi and vacuolar Pi. The cytoplasmic and vacuolarpHs could be determined by comparing the Pi chemical shiftswith the titration curve. When the external pH was changed overa range from pH 3 to 10, the cytoplasmic pH showed smaller changesthan the vacuolar pH, suggesting that the former is regulatedmore strictly than the latter. The H+-ATPase inhibitor, DCCD,caused the breakdown of the mechanism that regulates the intracellularpH. H+-ATPase appears to have an important part in the regulationof the intracellular pH. (Received January 4, 1984; Accepted August 27, 1984)  相似文献   
839.
Mycelial soluble proteins ofPholiota nameko labeled in vivo during the Pi-supplied (P+) and the Pi-depleted (P) cultures were separated by SDS-polyacrylamide gel electrophoresis and two-dimensional polyacrylamide gel electrophoresis, and visualized by fluorography. A comparison of protein profiles from the P+ and P cultures showed that Pi deficiency induces the synthesis of 15 polypeptides and an increase in the relative amount of 29 polypeptides. These result suggests that many proteins may be specifically synthesized de novo under Pi deficiency as part of the adaptive mechanism for this condition.  相似文献   
840.
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