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dc.contributor.authorMcLean, John William
dc.date.accessioned2012-07-18T23:37:54Z
dc.date.available2012-07-18T23:37:54Z
dc.date.issued1979
dc.identifier.urihttp://hdl.handle.net/10179/3625
dc.description.abstractFructose-1,6-bisphosphatase (FBPase, E.C. 3.1.3.11) has been purified from rat liver cytoplasm by a new purification procedure. Monospecific antibodies were raised to FBPase in rabbits to enable the immunochemical isolation and quantitation of FBPase in protein homogenates. Pulse labelling of rat liver in vivo showed that the synthesis of FBPase amounted to 0.89% of total soluble protein synthesis. Newly synthesized FBPase was found almost entirely in liver cytoplasm in contrast to serum albumin which was associated only with microsomes, and amounted to 16.7% of total microsomal protein synthesis. Isolated free and bound polysomes from liver synthesized almost equal amounts of FBPase when incubated in vitro, whereas albumin synthesis was confined to bound polysomes. Premature termination of translation led to the release of partial protein transcripts which were specifically immunoprecipitated. Affinity-purified 125 I-labelled antibodies to FBPase and albumin were used to quantitate nascent protein chains on free and bound polysomes. FBPase antibody bound to both classes of polysome with almost equal affinity but albumin antibody was only associated with bound polysomes. Poly(A)+ RNA isolated from free and bound polysomes by poly(U)-Sepharose chromatography was translated in a cell-free protein-synthesizing system derived from wheat germ. RNA from both classes of polysome synthesized FBPase, but albumin was only synthesized in response to bound polysomal RNA. Some full lengths transcripts corresponding to both proteins were produced in wheat germ extracts, but a large amount of smaller molecular weight material was specifically immunoprecipitated. Total translation products from both classes of polysome also produced considerable abnormally short molecular weight material, but only full length transcripts were produced when the system was programmed with TMV RNA. Since liver cells contain twice as many bound polysomes as free, it has been concluded that about 70% of intracellular FBPase synthesis takes place on bound polysomes. In contrast, albumin synthesis was almost totally confined (>97%) to bound polysomes and newly synthesized albumin was segregated into microsomes. The partitioning of synthetic activity for albumin is therefore a result of the distribution of mRNA coding for this protein.en
dc.language.isoenen
dc.publisherMassey Universityen_US
dc.rightsThe Authoren_US
dc.subjectRatsen
dc.subjectMetabolismen
dc.subjectFructoseen
dc.subjectSynthesisen
dc.titleThe intracellular site of synthesis of fructose 1,6-bisphosphatase in rat liver : a thesis presented in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Biochemistry at Massey Universityen
dc.typeThesisen
thesis.degree.disciplineBiochemistryen
thesis.degree.grantorMassey Universityen
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophy (Ph.D.)en


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