Intercellular spaces enhance potato tuber elasticity

Summary The intercellular volume within tuber tissue increases with tuber maturation. At the same time, both tuber injury after mechanical load and lentical perforation after water uptake by tubers in wet peat decreases. The degree of tuber injury is correlated with intercellular space (r=−0.667,n=16) and with water saturation of tissue (r=0.697,n=16). The tubers lose water during storage. In wet soil wilted tubers take up significantly higher amounts of water than turgid tubers, and lenticel perforation is much more frequent. Tuber maturation in autumn and low water loss during storage enhance the cushioning effect of the intercellular gas volume of tuber tissue against outside mechanical load and internal tension after water uptake.     

Mineral binding capacity of dephytinized insoluble fiber from extruded wheat,oat and rice brans

Insoluble fiber fractions from raw and extruded oat, rice and wheat brans were isolated and phytate removed. In vitro mineral binding studies were performed utilizing copper (Cu²⁺), calcium (Ca²⁺) and zinc (Zn²⁺) ions, which were added individually to enzymatically treated (Prosky et al., 1985), acid washed insoluble fiber residues from oat, rice and wheat brans. The enzymatic digestion step with alpha-amylase, protease and amyloglucosidase served to remove protein and starch from the samples. Mineral binding studies were performed on the insoluble fiber residue. Mineral content was determined by flame atomic absorption spectroscopy. Raw brans served as controls. A twin-screw extruder Model DNDG-62/20D, manufactured by Bühlerag (CH-9240, Uzwil, Switzerland) was utilized. The objectives of the study were to determine the total Cu²⁺, Ca²⁺ and Zn²⁺binding capacity of the dephytinized insoluble fiber from each bran; and to determine if extrusion screw speed affected the brans' insoluble fiber mineral binding capacity. Although dephytinized, the brans' insoluble fiber fraction bound Cu²⁺, Ca²⁺ and Zn²⁺ions. Oat bran bound more Cu²⁺, Ca²⁺ and Zn²⁺ than wheat bran, which bound more than rice bran. Extrusion processing did not affect the brans' insoluble fiber binding capacity to bind Cu²⁺. However, it increased the binding capacity of Ca²⁺ and Zn²⁺ of the insoluble fiber fraction from rice and oat brans.     

The Marek��s disease virus (MDV) protein encoded by the UL17 ortholog is essential for virus growth

Marek’s disease virus type 1 (MDV-1) shows a strict dependency on the direct cell-to-cell spread for its propagation in cell culture. As MDV-1 shows an impaired nuclear egress in cell culture, we wished to address the characterization of capsid/tegument genes which may intervene in the maturation of intranuclear capsids. Orthologs of UL17 are present in all herpesviruses and, in all reported case, were shown to be essential for viral growth, playing a role in capsid maturation and DNA packaging. As only HSV-1 and PrV UL17 proteins have been characterized so far, we wished to examine the role of MDV-1 pUL17 in virus replication. To analyze MDV-1 UL17 gene function, we created deletion mutants or point mutated the open reading frame (ORF) to interrupt its coding phase. We established that a functional ORF UL17 is indispensable for MDV-1 growth. We chose to characterize the virally encoded protein by tagging the 729 amino-acid long protein with a repeat of the HA peptide that was fused to its C-terminus. Protein pUL17 was identified in infected cell extracts as an 82 kDa protein which localized to the nucleus, colocalizing with VP5, the major capsid protein, and VP13/14, a major tegument protein. By using green fluorescent protein fusion and HA tagged proteins expressed under the cytomegalovirus IE gene enhancer/promoter (P_{CMV IE}), we showed that MDV-1 pUL17 nuclear distribution in infected cells is not an intrinsic property. Although our results strongly suggest that another viral protein retains (or relocate) pUL17 to the nucleus, we report that none of the tegument protein tested so far were able to mediate pUL17 relocation to the nucleus.     

Induced maturation and spawning: opportunities and applications for research on oogenesis

Broodstock management requires the ability to detect and regulate oocyte growth, acquisition of maturational competence, maturation of oocytes, and onset of ovarian atresia. Our research on temperate basses (genus Morone) has supported development of these capabilities. These investigations have revealed that accumulation of neutral lipid droplets and deposition of vitellogenin-derived yolk proteins in growing oocytes are independent processes with different sensitivities to changing day length and water temperature. In these fishes, completion of oocyte growth is marked by disappearance of vitellogenin from ovarian biopsy samples. Competence of females for induced spawning is predicted by the ability of biopsied follicles to initiate oocyte meiosis in vitro in response to insulin-like growth factor I. Cytoplasmic maturation of the oocytes is triggered by the maturation-inducing steroid hormone and can be monitored by evaluating degradation of the yolk proteins. Onset of ovarian atresia is indicated by the appearance of edema in the granulosa cell layer of biopsied follicles, and can be delayed for months by holding gravid females at abnormally low temperature (`cold banking'). These novel findings hold strong promise for application to other farmed fishes.