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Kateri A Duncan

Publications and source records attributed to Kateri A Duncan.

2 recordsLinked to original sources

The three maize sucrose synthase isoforms differ in distribution, localization, and phosphorylation.

Although sucrose synthase (SUS) is widely appreciated for its role in plant metabolism and growth, very little is known about the contribution of each of the SUS isoforms to these processes. Using isoform-specific antibodies, we evaluated the three known isoforms individually at the protein level. SUS1 and SUS-SH1 proteins have been studied previously; however, SUS2 (previously known as SUS3) has only been studied at the transcript level. Using SUS2 isoform-specific antibodies, we determined that this isoform is present in several maize tissues. The intracellular localization of all SUS isoforms was studied by cellular fractionation of leaves and developing kernels. Interestingly, SUS1 and SUS-SH1 were associated with membranes while SUS2 was not. The lack of membrane-associated SUS2 indicates that it might have a unique role in cytoplasmic sucrose metabolism. Using co-immunoprecipitation with kernel extracts, it was also established that SUS2 exists predominantly as a hetero-oligomer with SUS1, while SUS-SH1 forms only homo-oligomers. Using sequence-specific and phospho-specific antibodies, we have established for the first time that SUS-SH1 is phosphorylated in vivo at the Ser10 site in kernels, similar to the SUS1 Ser15 site. In midveins, additional evidence suggests that SUS can be phosphorylated at a novel C-terminal threonine site. Together, these results show that the isoforms of SUS are important in both cytosolic and membrane-associated sucrose degradation, but that their unique attributes most probably impart isoform-specific functional roles.

Cell Membrane↗

Determination of structural requirements and probable regulatory effectors for membrane association of maize sucrose synthase 1.

Sucrose (Suc) synthase (SUS) cleaves Suc to form UDP glucose and fructose, and exists in soluble and membrane-associated forms, with the latter proposed to channel UDP glucose to the cellulose-synthase complex on the plasma membrane of plant cells during synthesis of cellulose. However, the structural features responsible for membrane localization and the mechanisms regulating its dual intracellular localization are unknown. The maize (Zea mays) SUS1 isoform is likely to have the intrinsic ability to interact directly with membranes because we show: (1) partial membrane localization when expressed in Escherichia coli, and (2) binding to carbonate-stripped plant microsomes in vitro. We have undertaken mutational analyses (truncations and alanine substitutions) and in vitro microsome-binding assays with the SUS1 protein to define intrinsic membrane-binding regions and potential regulatory factors that could be provided by cellular microenvironment. The results suggest that two regions of SUS1 contribute to membrane affinity: (1) the amino-terminal noncatalytic domain, and (2) a region with sequence similarity to the C-terminal pleckstrin homology domain of human pleckstrin. Alanine substitutions within the pleckstrin homology-like domain of SUS1 reduced membrane association in E. coli and with plant microsomes in vitro without reducing enzymatic activity. Microsomal association of wild-type SUS1 displayed cooperativity with SUS1 protein concentration and was stimulated by both lowering the pH and adding Suc. These studies offer insight into the molecular level regulation of SUS1 localization and its participation in carbon partitioning in plants. Moreover, transgenics with active SUS mutants altered in membrane affinity may be of technological utility.

Amino Acid Sequence↗