GLOBOSA (GLO) is a homeotic gene whose mutants show sepaloid petals and carpelloid stamens. The similarity of Glo mutants to those of the DEFICIENS (DEFA) gene suggests that the two genes have comparable functions in floral morphogenesis. The GLO cDNA has been cloned by virtue of its homology to the MADS‐box, a conserved DNA‐binding domain also contained in the DEFA gene. We have determined the structure of the wild type GLO gene as well as of several glo mutant alleles which contain transposable element insertions responsible for somatic and germinal instability of Glo mutants. Analyses of the temporal and spatial expression patterns of the DEFA and GLO genes during development of wild type flowers and in flowers of various stable and unstable defA and glo alleles indicate independent induction of DEFA and GLO transcription. In contrast, organ‐specific up‐regulation of the two genes in petals and stamens depends on expression of both DEFA and GLO. In vitro DNA‐binding studies were used to demonstrate that the DEFA and GLO proteins specifically bind, as a heterodimer, to motifs in the promoters of both genes. A model is presented which proposes both combinatorial and cross‐regulatory interactions between the DEFA and GLO genes during petal and stamen organogenesis in the second and third whorls of the flower. The function of the two genes controlling determinate growth of the floral meristem is also discussed.

The encapsulation of high amounts of magnetite into polystyrene particles can efficiently be achieved by a new three‐step preparation route including two miniemulsion processes. In the first step, a dispersion of oleic acid coated magnetite particles in octane is obtained. In the second step, magnetite aggregates in water are produced in a miniemulsion process by using sodium dodecyl sulfate (SDS) as surfactant. In the third step, the dispersion with the magnetite aggregates which are covered by an oleic acid/SDS bilayer were mixed with a monomer miniemulsion and a second miniemulsion process, an ad‐miniemulsification process, is used to obtain full encapsulation. After polymerization, polymer encapsulated magnetite aggregates were obtained. Characterization by thermogravimetry, preparative ultracentrifugation, and transmission electron microscopy showed that up to 40% magnetite could be encapsulated resulting in particles with a high homogeneity of the magnetite content. Magnetometry measurements reveal that the included iron oxide aggregates still consist of separated superparamagnetic magnetite particles. Transmission electron micrograph for magnetite polystyrene particles (Latex‐1).magnified imageTransmission electron micrograph for magnetite polystyrene particles (Latex‐1).

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The process of miniemulsification allows the generation of small, homogeneous, and stable droplets containing monomer or polymer precursors and magnetite which are then transferred by polymer reactions to the final polymer latexes, keeping their particular identity without serious exchange kinetics involved. It is shown that the miniemulsion process can excellently be used for the formulation of polymer-coated magnetic nanoparticles which can further be used for biomedical applications. The use of high shear, appropriate surfactants, and the addition of a hydrophobe in order to suppress the influence of Ostwald ripening are key factors for the formation of the small and stable droplets in miniemulsion and will be discussed. Two different approaches based on miniemulsion processes for the encapsulation of magnetite into polymer particles will be presented in detail.