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TSK gel permeation chromatography of non-granular starches, amylopectin chain-length distributions measured by HPAEC-PAD, and DSC characteristics of starches of maize endosperms possessing different alleles at the amylose-extender (ae) loci were studied. GPC of non-granular starches through Toyopearl columns showed that elution profiles for 5 ae mutants, Oh43 inbred line ae (standard ae), ae- RWB-2 and ae-RWB-3, and W23xL317 hybrid line ae-PP and ae-Bol 561, were similar to a commercial ae starch, Hylon VII and different from Hylon ae starch and normal maize starches. The elution profile for W23xL317 ae-emll was similar to Hylon and different from Hylon and normal maize starches. HPAEC-PAD of isoamylase-debranched starches showed that the 5 ae mutants were uniquely ae type similar to Hylon VII and different from Hylon V. W23xL137 ae-emll had the amylopectin chain-length distribution similar to Hylon . Gelatinization temperatures (Tp) of the ae starches measured by a Setaram Micro DSC III were high compared with the normal counterpart starches except for Oh43 ae-RWB-1 starch. Oh43 ae-RWB-1 starch had structure and thermal characteristics similar to the normal maize starch.
The starch and protein in wheat (Triticum aestivum L.) endosperm provide 20% of the calories eaten by humans and were heavily selected for during domestication. We examined the main storage products and gene expression patterns that may embody compositional differences between two wild species Aegilops crassa and Aegilops tauschii and cultivated bread wheat. The storage product profiles differed significantly with T. aestivum accumulating twice as much carbon as the wild species, while the latter had 1.5 to 2-fold more total nitrogen per seed. Transcriptional analyses of endosperms of similar fresh weight were compared using a cDN A macroarray. Aegilops tauschii, and especially Ae. crassa had stronger hybridizations with storage protein sequences, but while there were differences in transcripts for starch biosynthetic genes, they were less dramatic. Of these, we cloned the Starch Branching Enzymes (SBE) IIa promoter region and the genomic clone of the Brittle-1 (Bt1) ADPglucose transporter. While Ae. crassa SBEIIa sequence was more divergent than that of Ae. tauschii 's compared to bread wheat, there were no sequence polymorphisms that would explain the observed expression differences in Btl between these species. Furthermore, while there were nucleotide differences between Btl in Ae. crassa and bread wheat, they were synonymous at the amino acid level. Some of transcriptional differences identified here, however, deserve further examination as part of a strategy to manipulate wheat starch and protein composition.
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