Changes in the Expression of Membrane Antigens During the Differentiation of Chicken Erythroblasts

Chicken erythroblasts can be transformed by the avian retrovirus, avian erythroblastosis virus (AEV). Earlier studies have shown that the mechanism of transformation appears to involve a “block” in differentiation, in that when erythroblasts are transformed by a temperature-sensitive mutant of ts34 AEV and incubated at the nonpermissive temperature, the cells start to differentiate and produce hemoglobin. We have decided to use this system to isolate pure populations of chicken erythroblasts and raise monoclonal antibodies against their cell surface proteins. Three monoclonal antibodies were isolated and tested for their ability to bind to various hematopoietic cell types; two were shown to be erythroid-specific, whereas the other antibody bound to proliferating cells but not to erythrocytes or granulocytes. Of the erythroid-specific antibodies, one precipitated a 94,000 molecular weight protein, whereas the other precipitated a 11,000 molecular weight protein that was tentatively identified as hemoglobin. The use of this system and approach to identify and evaluate changes that occur during the differentiation is discussed.     

Insights into erythroid differentiation obtained from studies on avian erythroblastosis virus

Analysis of the oncogenes v-erbB and v-erbA and their normal proto-oncogene counterparts has revealed several novel aspects of erythroid differentiation. A new erythroid progenitor capable of extended self-renewal has been described, tyrosine kinase receptors and steroid hormone receptors have been found to cooperate in controlling self-renewal, and dramatic alterations in the cell cycle have been found to accompany induction of terminal differentiation.     

A rapid radiometric assay for dihydrofolate reductase

A rapid radiochemical procedure for the measurement of dihydrofolate reductase activity is described. The method employs separation of the radiolabeled substrate from the products of the reaction by precipitation with acetic acid and zinc sulfate. This method permits rapid processing of samples and climinates time-consumlng column chromatography techniques. Good agreement of results is obtained when the radioactive method is compared to the spectrophotometric assay method.     

Major phosphoprotein of avian sarcoma virus: peptide analysis of the variously charged species.

The 19,000 dalton phosphoprotein (pp19) of avian sarcoma virus strain B77 isolated by guanidine-agarose chromatography was further resolved into multiple charged species by DEAE-cellulose chromatography. A comparison of the tryptic peptide maps of ¹²⁵I-iodinated lowly phosphorylated and highly phosphorylated species of the pp19 suggested that the same polypeptide occurs in the virion in different phosphorylated states.     

Carotenoid Biosynthesis in Rhodotorula glutinis

It was determined that lycopene could be cyclized directly by Rhodotorula glutinis. It was also shown the the temperature effect (i.e., increased beta-carotene synthesis in response to lower incubation temperatures) in R. glutinis was controlled by changes in enzyme concentration.     

The management of populations of vesicular-arbuscular mycorrhizal fungi in acid-infertile soils of a savanna ecosystem

Topsoil stockpiled for 4 years resulted in an accumulation of NH₄-N at depths of 1m or more in mound, as measured by an ammonia gas-sensing electrode. When leached with water these soils were also found to contain high concentrations of dissolved organic C below 1m. Both NH₄-N and DOC were products of microbial mineralisation of soil organic matter that accumulated under anaerobic conditions. When these soils were restored a flush of decomposition took place, fuelled by labile organic matter and soluble nitrogen.Stockpiled soil which underwent an ammonium-rich perfusion regime in the laboratory indicated that in-mound soils rapidly attained greater nitrification potential than surface mound soils and also had greater potential for further mineralisation of organic matter to NH₄-N. This further production was seen as a contribution from the bacterial flush, stimulated by the large labile-C pool already present.As the bulk of stored soil was anaerobic, restored soils were seen as potentially wasteful of their N-reserves; the fate of nitrogen and soluble carbon compounds in restored soils is discussed.