{"title":"玉米叶片叶肉和束鞘细胞中的淀粉磷酸化酶同工酶","authors":"Christian Mateyka, Claus Schnarrenberger","doi":"10.1016/0304-4211(84)90245-1","DOIUrl":null,"url":null,"abstract":"<div><p>Starch phosphorylase from leaves of the C<sub>4</sub>-plant corn (<em>Zea mays</em> L.) could be separated into two peaks of activity by chromatography on DEAE-cellulose (or by (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub> gradient solubilization). Subsequent polyacrylamide gel electrophoresis under native conditions revealed a slowly migrating phosphorylase for the peak eluting first from DEAE-cellulose and a major, fast migrating phosphorylase for the peak eluting second. The latter peak contained also two very minor bands which migrated even faster than the other two phosphorylases. When phosphorylases were extracted from mesophyll protoplasts and from bundle sheath strands (isolated by the enzymatic isolation procedure) it was the slowly migrating phosphorylase which was associated with the mesophyll cells and the major, fast migrating phosphorylase which originated from the bundle sheath cells. The findings are discussed in view of similar isoenzymes of phosphorylase reported for chloroplasts and cytosol in leaves of C<sub>3</sub>-plants.</p></div>","PeriodicalId":20221,"journal":{"name":"Plant Science Letters","volume":"36 2","pages":"Pages 119-123"},"PeriodicalIF":0.0000,"publicationDate":"1984-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0304-4211(84)90245-1","citationCount":"8","resultStr":"{\"title\":\"Starch phosphorylase isoenzymes in mesophyll and bundle sheath cells of corn leaves\",\"authors\":\"Christian Mateyka, Claus Schnarrenberger\",\"doi\":\"10.1016/0304-4211(84)90245-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Starch phosphorylase from leaves of the C<sub>4</sub>-plant corn (<em>Zea mays</em> L.) could be separated into two peaks of activity by chromatography on DEAE-cellulose (or by (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub> gradient solubilization). Subsequent polyacrylamide gel electrophoresis under native conditions revealed a slowly migrating phosphorylase for the peak eluting first from DEAE-cellulose and a major, fast migrating phosphorylase for the peak eluting second. The latter peak contained also two very minor bands which migrated even faster than the other two phosphorylases. When phosphorylases were extracted from mesophyll protoplasts and from bundle sheath strands (isolated by the enzymatic isolation procedure) it was the slowly migrating phosphorylase which was associated with the mesophyll cells and the major, fast migrating phosphorylase which originated from the bundle sheath cells. The findings are discussed in view of similar isoenzymes of phosphorylase reported for chloroplasts and cytosol in leaves of C<sub>3</sub>-plants.</p></div>\",\"PeriodicalId\":20221,\"journal\":{\"name\":\"Plant Science Letters\",\"volume\":\"36 2\",\"pages\":\"Pages 119-123\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1984-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0304-4211(84)90245-1\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Science Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0304421184902451\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Science Letters","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0304421184902451","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Starch phosphorylase isoenzymes in mesophyll and bundle sheath cells of corn leaves
Starch phosphorylase from leaves of the C4-plant corn (Zea mays L.) could be separated into two peaks of activity by chromatography on DEAE-cellulose (or by (NH4)2SO4 gradient solubilization). Subsequent polyacrylamide gel electrophoresis under native conditions revealed a slowly migrating phosphorylase for the peak eluting first from DEAE-cellulose and a major, fast migrating phosphorylase for the peak eluting second. The latter peak contained also two very minor bands which migrated even faster than the other two phosphorylases. When phosphorylases were extracted from mesophyll protoplasts and from bundle sheath strands (isolated by the enzymatic isolation procedure) it was the slowly migrating phosphorylase which was associated with the mesophyll cells and the major, fast migrating phosphorylase which originated from the bundle sheath cells. The findings are discussed in view of similar isoenzymes of phosphorylase reported for chloroplasts and cytosol in leaves of C3-plants.