Maize starch-branching enzyme isoforms and amylopectin structure. In the absence of starch-branching enzyme IIb, the further absence of starch-branching enzyme Ia leads to increased branching

Previous studies indicated that the deficiency of starch-branching enzyme (SBE) Ia in the single mutant sbe1a::Mu (sbe1a) has no impact on endosperm starch structure, whereas the deficiency of SBEIIb in the ae mutant is well known to reduce the branching of starch. We hypothesized that in maize (Zea...

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Veröffentlicht in:Plant physiology (Bethesda) 2004-11, Vol.136 (3), p.3515-3523
Hauptverfasser: Yao, Y, Thompson, D.B, Guiltinan, M.J
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description Previous studies indicated that the deficiency of starch-branching enzyme (SBE) Ia in the single mutant sbe1a::Mu (sbe1a) has no impact on endosperm starch structure, whereas the deficiency of SBEIIb in the ae mutant is well known to reduce the branching of starch. We hypothesized that in maize (Zea mays) endosperm, the function of SBEIIb is predominant to that of SBEIa, and SBEIa would have an observable effect only on amylopectin structure in the absence of SBEIIb. To test this hypothesis, the mutant sbe1a was introgressed into lines containing either wx (lacking the granule-bound starch synthase GBSSI) or ae wx (lacking both SBEIIb and GBSSI) in the W64A background. Both western blotting and zymogram analysis confirmed the SBEIa deficiency in sbe1a wx and sbe1a ae wx, and the SBEIIb deficiency in ae wx and sbe1a ae wx. Using zymogram analysis, no pleiotropic effects of sbe1a genes on SBEIIa, starch synthase, or starch-debranching enzyme isoforms were observed. High-performance size exclusion chromatography analysis shows that the chain-length profiles of amylopectin as well as beta-limit dextrin were indistinguishable between wx and sbe1a wx, whereas significant differences for both were observed between ae wx and sbe1a ae wx, suggesting an effect of SBEIa on amylopectin biosynthesis that is observable only in the absence of SBEIIb. The amylopectin branch density and the average number of branches per cluster were both higher in endosperm starch from sbe1a ae wx than from ae wx. These results indicate possible functional interactions between SBE isoforms that may involve enzymatic inhibition. Both the cluster repeat distance and the distance between branch points on the short intracluster chains were similar for all genotypes however, suggesting a similar pattern of individual SBE isoforms in cluster initiation and the determination of branch point location.
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In the absence of starch-branching enzyme IIb, the further absence of starch-branching enzyme Ia leads to increased branching</title><source>MEDLINE</source><source>JSTOR Archive Collection A-Z Listing</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Yao, Y ; Thompson, D.B ; Guiltinan, M.J</creator><creatorcontrib>Yao, Y ; Thompson, D.B ; Guiltinan, M.J</creatorcontrib><description>Previous studies indicated that the deficiency of starch-branching enzyme (SBE) Ia in the single mutant sbe1a::Mu (sbe1a) has no impact on endosperm starch structure, whereas the deficiency of SBEIIb in the ae mutant is well known to reduce the branching of starch. We hypothesized that in maize (Zea mays) endosperm, the function of SBEIIb is predominant to that of SBEIa, and SBEIa would have an observable effect only on amylopectin structure in the absence of SBEIIb. To test this hypothesis, the mutant sbe1a was introgressed into lines containing either wx (lacking the granule-bound starch synthase GBSSI) or ae wx (lacking both SBEIIb and GBSSI) in the W64A background. Both western blotting and zymogram analysis confirmed the SBEIa deficiency in sbe1a wx and sbe1a ae wx, and the SBEIIb deficiency in ae wx and sbe1a ae wx. Using zymogram analysis, no pleiotropic effects of sbe1a genes on SBEIIa, starch synthase, or starch-debranching enzyme isoforms were observed. High-performance size exclusion chromatography analysis shows that the chain-length profiles of amylopectin as well as beta-limit dextrin were indistinguishable between wx and sbe1a wx, whereas significant differences for both were observed between ae wx and sbe1a ae wx, suggesting an effect of SBEIa on amylopectin biosynthesis that is observable only in the absence of SBEIIb. The amylopectin branch density and the average number of branches per cluster were both higher in endosperm starch from sbe1a ae wx than from ae wx. These results indicate possible functional interactions between SBE isoforms that may involve enzymatic inhibition. 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Psychology ; Gels ; Gene Expression Regulation, Plant - genetics ; genetic variation ; Genotype ; Genotypes ; grain crops ; hexosyltransferases ; Isoenzymes - genetics ; Isoenzymes - metabolism ; isozymes ; Metabolism ; Mutation ; Phenotype ; phenotypic variation ; Photosynthesis, respiration. 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In the absence of starch-branching enzyme IIb, the further absence of starch-branching enzyme Ia leads to increased branching</title><title>Plant physiology (Bethesda)</title><addtitle>Plant Physiol</addtitle><description>Previous studies indicated that the deficiency of starch-branching enzyme (SBE) Ia in the single mutant sbe1a::Mu (sbe1a) has no impact on endosperm starch structure, whereas the deficiency of SBEIIb in the ae mutant is well known to reduce the branching of starch. We hypothesized that in maize (Zea mays) endosperm, the function of SBEIIb is predominant to that of SBEIa, and SBEIa would have an observable effect only on amylopectin structure in the absence of SBEIIb. To test this hypothesis, the mutant sbe1a was introgressed into lines containing either wx (lacking the granule-bound starch synthase GBSSI) or ae wx (lacking both SBEIIb and GBSSI) in the W64A background. Both western blotting and zymogram analysis confirmed the SBEIa deficiency in sbe1a wx and sbe1a ae wx, and the SBEIIb deficiency in ae wx and sbe1a ae wx. Using zymogram analysis, no pleiotropic effects of sbe1a genes on SBEIIa, starch synthase, or starch-debranching enzyme isoforms were observed. High-performance size exclusion chromatography analysis shows that the chain-length profiles of amylopectin as well as beta-limit dextrin were indistinguishable between wx and sbe1a wx, whereas significant differences for both were observed between ae wx and sbe1a ae wx, suggesting an effect of SBEIa on amylopectin biosynthesis that is observable only in the absence of SBEIIb. The amylopectin branch density and the average number of branches per cluster were both higher in endosperm starch from sbe1a ae wx than from ae wx. These results indicate possible functional interactions between SBE isoforms that may involve enzymatic inhibition. Both the cluster repeat distance and the distance between branch points on the short intracluster chains were similar for all genotypes however, suggesting a similar pattern of individual SBE isoforms in cluster initiation and the determination of branch point location.</description><subject>1,4-alpha-Glucan Branching Enzyme - genetics</subject><subject>1,4-alpha-Glucan Branching Enzyme - metabolism</subject><subject>amylopectin</subject><subject>Amylopectin - chemistry</subject><subject>Amylopectin - metabolism</subject><subject>Biochemical Processes and Macromolecular Structures</subject><subject>Biological and medical sciences</subject><subject>Biosynthesis</subject><subject>Branching</subject><subject>Corn</subject><subject>Dextrins</subject><subject>Endosperm</subject><subject>Enzymes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gels</subject><subject>Gene Expression Regulation, Plant - genetics</subject><subject>genetic variation</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>grain crops</subject><subject>hexosyltransferases</subject><subject>Isoenzymes - genetics</subject><subject>Isoenzymes - metabolism</subject><subject>isozymes</subject><subject>Metabolism</subject><subject>Mutation</subject><subject>Phenotype</subject><subject>phenotypic variation</subject><subject>Photosynthesis, respiration. Anabolism, catabolism</subject><subject>Plant physiology and development</subject><subject>Protein isoforms</subject><subject>seeds</subject><subject>starch</subject><subject>starch granules</subject><subject>starch synthase</subject><subject>starch-branching enzyme</subject><subject>starch-debranching enzyme</subject><subject>Starches</subject><subject>Zea mays</subject><subject>Zea mays - enzymology</subject><subject>Zea mays - genetics</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk9v1DAQxSMEotvCkRsCX8qJLHZiO86BA6r4s1IRB-jZmjjj3VSJHewEafvl-Go47GoLByROb6T5vZmRn7PsGaNrxih_M47rJGvKy5KJB9mKibLIC8HVw2xFaaqpUvVZdh7jLaWUlYw_zs6YEEwKxlfZz8_Q3SGJEwSzy5sAzuw6tyXo7vYDki5668MQCbiWwLDv_Yhm6lwyhNlMc8A12Tgy7ZBAE9EZJN7-c9pm07z-zdo5JAn_5QHSI7SRTJ50zgSEiC05YU-yRxb6iE-PepHdfHj_7epTfv3l4-bq3XVuhCymvJAVb5SsS1Uw2TQM0IIqAIE2VSulwVQZyhkXgkODLTWyarGqFVhjJTXlRfb2MHecmwFbg24K0OsxdAOEvfbQ6b87rtvprf-hRVExwZL_1dEf_PcZ46SHLhrse3Do56hlRWXNlEpgfgBN8DEGtKcdjOolcT2OepFD4ol_8edh9_Qx4gRcHgGIBnq7vFwX7zlZJo4v3PMDdxsnH059Xop027Ln5aFtwWvYhjTi5muRPhSltWQqEb8Ap7rMpg</recordid><startdate>20041101</startdate><enddate>20041101</enddate><creator>Yao, Y</creator><creator>Thompson, D.B</creator><creator>Guiltinan, M.J</creator><general>American Society of Plant Biologists</general><general>American Society of Plant Physiologists</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20041101</creationdate><title>Maize starch-branching enzyme isoforms and amylopectin structure. In the absence of starch-branching enzyme IIb, the further absence of starch-branching enzyme Ia leads to increased branching</title><author>Yao, Y ; Thompson, D.B ; Guiltinan, M.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c562t-2674b86938216bb1aefa82aea0b7d66ceea0c0414554abed0c67de798afcf60c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>1,4-alpha-Glucan Branching Enzyme - genetics</topic><topic>1,4-alpha-Glucan Branching Enzyme - metabolism</topic><topic>amylopectin</topic><topic>Amylopectin - chemistry</topic><topic>Amylopectin - metabolism</topic><topic>Biochemical Processes and Macromolecular Structures</topic><topic>Biological and medical sciences</topic><topic>Biosynthesis</topic><topic>Branching</topic><topic>Corn</topic><topic>Dextrins</topic><topic>Endosperm</topic><topic>Enzymes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gels</topic><topic>Gene Expression Regulation, Plant - genetics</topic><topic>genetic variation</topic><topic>Genotype</topic><topic>Genotypes</topic><topic>grain crops</topic><topic>hexosyltransferases</topic><topic>Isoenzymes - genetics</topic><topic>Isoenzymes - metabolism</topic><topic>isozymes</topic><topic>Metabolism</topic><topic>Mutation</topic><topic>Phenotype</topic><topic>phenotypic variation</topic><topic>Photosynthesis, respiration. Anabolism, catabolism</topic><topic>Plant physiology and development</topic><topic>Protein isoforms</topic><topic>seeds</topic><topic>starch</topic><topic>starch granules</topic><topic>starch synthase</topic><topic>starch-branching enzyme</topic><topic>starch-debranching enzyme</topic><topic>Starches</topic><topic>Zea mays</topic><topic>Zea mays - enzymology</topic><topic>Zea mays - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yao, Y</creatorcontrib><creatorcontrib>Thompson, D.B</creatorcontrib><creatorcontrib>Guiltinan, M.J</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yao, Y</au><au>Thompson, D.B</au><au>Guiltinan, M.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maize starch-branching enzyme isoforms and amylopectin structure. In the absence of starch-branching enzyme IIb, the further absence of starch-branching enzyme Ia leads to increased branching</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>2004-11-01</date><risdate>2004</risdate><volume>136</volume><issue>3</issue><spage>3515</spage><epage>3523</epage><pages>3515-3523</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><coden>PPHYA5</coden><abstract>Previous studies indicated that the deficiency of starch-branching enzyme (SBE) Ia in the single mutant sbe1a::Mu (sbe1a) has no impact on endosperm starch structure, whereas the deficiency of SBEIIb in the ae mutant is well known to reduce the branching of starch. We hypothesized that in maize (Zea mays) endosperm, the function of SBEIIb is predominant to that of SBEIa, and SBEIa would have an observable effect only on amylopectin structure in the absence of SBEIIb. To test this hypothesis, the mutant sbe1a was introgressed into lines containing either wx (lacking the granule-bound starch synthase GBSSI) or ae wx (lacking both SBEIIb and GBSSI) in the W64A background. Both western blotting and zymogram analysis confirmed the SBEIa deficiency in sbe1a wx and sbe1a ae wx, and the SBEIIb deficiency in ae wx and sbe1a ae wx. Using zymogram analysis, no pleiotropic effects of sbe1a genes on SBEIIa, starch synthase, or starch-debranching enzyme isoforms were observed. High-performance size exclusion chromatography analysis shows that the chain-length profiles of amylopectin as well as beta-limit dextrin were indistinguishable between wx and sbe1a wx, whereas significant differences for both were observed between ae wx and sbe1a ae wx, suggesting an effect of SBEIa on amylopectin biosynthesis that is observable only in the absence of SBEIIb. The amylopectin branch density and the average number of branches per cluster were both higher in endosperm starch from sbe1a ae wx than from ae wx. These results indicate possible functional interactions between SBE isoforms that may involve enzymatic inhibition. Both the cluster repeat distance and the distance between branch points on the short intracluster chains were similar for all genotypes however, suggesting a similar pattern of individual SBE isoforms in cluster initiation and the determination of branch point location.</abstract><cop>Rockville, MD</cop><pub>American Society of Plant Biologists</pub><pmid>15516514</pmid><doi>10.1104/pp.104.043315</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects 1,4-alpha-Glucan Branching Enzyme - genetics
1,4-alpha-Glucan Branching Enzyme - metabolism
amylopectin
Amylopectin - chemistry
Amylopectin - metabolism
Biochemical Processes and Macromolecular Structures
Biological and medical sciences
Biosynthesis
Branching
Corn
Dextrins
Endosperm
Enzymes
Fundamental and applied biological sciences. Psychology
Gels
Gene Expression Regulation, Plant - genetics
genetic variation
Genotype
Genotypes
grain crops
hexosyltransferases
Isoenzymes - genetics
Isoenzymes - metabolism
isozymes
Metabolism
Mutation
Phenotype
phenotypic variation
Photosynthesis, respiration. Anabolism, catabolism
Plant physiology and development
Protein isoforms
seeds
starch
starch granules
starch synthase
starch-branching enzyme
starch-debranching enzyme
Starches
Zea mays
Zea mays - enzymology
Zea mays - genetics
title Maize starch-branching enzyme isoforms and amylopectin structure. In the absence of starch-branching enzyme IIb, the further absence of starch-branching enzyme Ia leads to increased branching
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