. Interestingly, we revealed that the transport activity of ZmBT1 is reversibly regulated by redox reagents such as diamide and dithiothreitol. The expression of ZmBT1 is restricted to endosperm tissues during starch synthesis, whereas a recently identified BT1 maize homologue, the ZmBT1-2, exhibits a ubiquitous expression pattern in hetero-and autotrophic tissues indicating different physiological roles for both maize BT1 isoforms. BT1 homologues are present in both mono-and dicotyledonous plants. Phylogenetic analyses classify the BT1 family into two phylogenetically and biochemically distinct groups. The first group comprises BT1 orthologues restricted to cereals where they mediate the ADP-Glc transport into cereal endosperm storage plastids during starch synthesis. The second group occurs in mono-and dicotyledonous plants and is most probably involved in the export of adenine nucleotides synthesized inside plastids.Cereal crops accumulate starch in seed endosperm plastids as main energy reserve. The pathway of starch synthesis in cereal endosperms is unique and requires enzyme isoforms that are not present in other tissues or non-cereal plants. The ability of heterotrophic plastids to utilize cytosolic precursors to support their biosynthetic and catabolic pathways depends on the presence of specific transporters in the plastid envelope. In cereal endosperms, the ADP-glucose pyrophosphorylase (AGPase), 2 which catalyzes the first committed and rate-limiting step in starch biosynthesis, is mainly localized in the cytosol with a total AGPase activity of about 85-95% (2). Therefore, ADP-glucose (ADP-Glc) is synthesized in the cytosol of cereal endosperms as the main precursor for starch synthesis and has to be subsequently imported into the storage plastids.Several maize (Zea mays L.) endosperm mutants affected in starch quality or quantity were used to elucidate critical steps in amyloplast starch synthesis. The Waxy gene, which encodes a starch-granule-bound starch synthase involved in amylose synthesis (3) and the Shrunken-2 and Brittle-2 genes, which encode subunits of the AGPase (4 -6), were shown to be important for starch synthesis in maize. The Brittle-1 (BT1) maize mutant was identified in 1926 (7, 8) and corresponding endosperm is severely reduced in starch content, which results in kernels with a collapsed angular appearance at maturity. The BT1 protein from Z. mays (ZmBT1) belongs to the mitochondrial carrier family and is located in the amyloplast envelope membrane (9, 10). The absence of ZmBT1 correlates with a 12-fold higher level of ADP-Glc in the cytosol of BT1 mutant endosperm than in wild-type endosperm (11) and BT1 mutant kernels accumulate about 80% less starch than wild-type kernels (12). The incorporation of externally applied ADP-Glc into starch in amyloplasts isolated from BT1 mutant endosperm was reduced to about 25% compared with wild-type amyloplasts (13). These results indicate that ZmBT1 is involved in the transport of ADP-Glc into maize endosperm plastids (14), but up to now, no d...