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H Frick

Publications and source records attributed to H Frick.

24 records · Page 2Linked to original sources
PubMed1977

Influence of Helminthosporium maydis, Race T, Toxin on Potassium Uptake in Maize Roots: II. Sensitivity of Development of the Augmented Uptake Potential to Toxin and Inhibitors of Protein Synthesis.

Basal K(+) uptake in the root midzone region (cm 2 + 3 + 4) of N and T cytoplasmic versions of each of four maize inbreds was equally sensitive to the toxin(s) of Helminthosporium maydis, race T. Basal K(+) uptake in the root apex (0-1 cm) and augmented K(+) uptake in the root midzone were more toxin-sensitive in inbreds W64A(T) and Mo17(T) than in inbreds W64A(N) and Mo17(N). This differential response of N and T cytoplasms to toxins was not found for corresponding cytoplasms of inbreds WF9 and B37.Development of the augmented K(+) uptake rate in midzone segments of W64A(T) was blocked by a toxin concentration which did not affect augmentation development in W64A(N). Augmentation development was more toxin-sensitive in T than in N cytoplasmic versions of all inbreds tested. Fertility-restoring nuclear loci decreased but did not eliminate the toxin sensitivity of augmentation developments as observed in root midzones of inbred A619(T). Chloramphenicol-and/or cycloheximide-sensitive protein synthesis was required for augmentation development, but not for expression of either basal or augmented K(+) uptake.

Journal Article↗
PubMed1976

Influence of Helminthosporium maydis, Race T, Toxin on Potassium Uptake in Maize Roots.

The effect of a toxin extract of Helminthosporium maydis, race T on K(+) ((86)Rb) uptake by excised root segments of normal (N) and Texas cytoplasmic male-sterile (T) versions of corn inbred W64A was investigated. The uptake of K(+) was inhibited in both N and T roots by the toxin. This was true for both basal (freshly excised) and augmented (pretreated with aeration) K(+) uptake. Augmented uptake was more toxin-sensitive than basal uptake (irrespective of cytoplasm type), and the augmented uptake in T roots was seven to eight times more toxin-sensitive than in N roots.Specific zones of roots differed in their basal and augmented K(+) uptake rates as well as their toxin sensitivities. The root apex of T was more sensitive to toxin than the apex of N roots when basal K(+) uptake was measured. In mature zones of the root, T was more sensitive than N when augmented rates were measured. During the development of the augmented K(+) uptake capacity in either N or T roots, the sensitivity to the toxin did not change; uptake in N roots was inhibited by 10 to 25% and uptake in T roots was inhibited by 70 to 80%.The difference in toxin sensitivity of K(+) uptake between N and T roots may be due to N possessing a protective mechanism which is deficient in T.

Journal Article↗
PubMedDate not supplied

Modification of membrane protein expression and protein secretion in LLC-PK1 cultures grown on different carbohydrates.

Membrane glycoproteins and glycolipids play an important role in epithelial organization, transport and function. To study the effects of exogenous carbohydrates on the expression of glycoproteins, cells of the renal epithelial line LLC-PK1 were cultured on different nutritive carbohydrate sources and on uridine, which is, despite striking differences, known to substitute all essential nutritive functions of glucose. LLC-PK1 cultures were long-term adapted to growth in culture medium containing 0.5, 5, 10 and 25 mM glucose, and 5 mM fructose, galactose and uridine, respectively, as the sole carbohydrate source. These growth conditions elicited adaptive changes in the expression of enzyme activities of alkaline phosphatase and gamma-glutamyltranspeptidase, integral membrane glycoproteins exclusively localized in the apical membrane of LLC-PK1 cells. SDS-PAGE of membrane preparations of adapted LLC-PK1 cells revealed a strong induction of several protein bands between 13.5 and 47 kD in fructose-grown cells, while in plasma membranes of cells grown in galactose several protein bands between 62 and 70 kD decreased. Changes in the secretion pattern of proteins into the culture medium were most prominent in uridine-grown cells compared to controls grown on 25 mM glucose.

Alkaline Phosphatase↗