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Using chain-length distributions to diagnose genetic diversity in starch biosynthesis
被引:19
|作者:
Cuevas, Rosa Paula
[1
,2
]
Daygon, Venea Dara
[1
]
Morell, Matthew K.
[3
]
Gilbert, Robert G.
[2
]
Fitzgerald, Melissa A.
[1
]
机构:
[1] Int Rice Res Inst, Dapo 7777, Metro Manila, Philippines
[2] Univ Queensland, Ctr Nutr & Food Sci, Sch Land Crop & Food Sci, Brisbane, Qld 4072, Australia
[3] CSIRO Food Futures Flagship, Canberra, ACT 2601, Australia
关键词:
Starch;
Gelatinisation temperature;
Chain-length distribution;
lnN plot;
SINGLE-NUCLEOTIDE POLYMORPHISMS;
HIGH-AMYLOSE MUTANTS;
ORYZA-SATIVA L;
RICE ENDOSPERM;
SYNTHASE-IIA;
PHYSICOCHEMICAL PROPERTIES;
AMYLOPECTIN STRUCTURE;
BRANCHING ENZYME;
HIGH-TEMPERATURE;
MAIZE ENDOSPERM;
D O I:
10.1016/j.carbpol.2010.02.004
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Amylopectin synthesis is controlled by the coordinated action of several types of enzymes, including starch synthases, branching and debranching enzymes. The contributions of some of these enzymes to the building of starch molecules have been previously established. Changes to the activity of an enzyme can affect amylopectin structure, which is associated with diversity in functional properties. One such property, gelatinisation temperature, has been studied at the genetic, biochemical and phenotypic level. A technique, the 'log(number distribution) approach', offers a means of collecting normalisation-free representations of the chain-length distributions of starch, with the potential to reveal new information about kinetics and processes of starch synthesis; this method of plotting the data can potentially reveal much more than that usually employed, viz., the simple number chain-length distribution. In this study, samples from genotypes with defined mutations in starch biosynthetic genes that specifically and differently alter the chain-length distribution of single-cluster chains, with a resultant effect on gelatinisation temperature, are used to show that log(number distribution) plots have sufficient discriminative capacity to diagnose the gene affected by mutations, provide new information, and determine those features of the plot which associate with genotype and phenotype. (C) 2010 Elsevier Ltd. All rights reserved.
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页码:120 / 127
页数:8
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