Abstract. We have introduced into Hansenula polymorpha an extra copy of its alcohol oxidase gene. This gene which is under the control of the Saccharomyces cerevisiae phosphoglycerate kinase promoter is integrated in a chromosome different from the one conmining the endogenous gene. Cells with the extra alcohol oxidase gene, grown on glucose or ethanol as the sole carbon source, express enzymatically active alcohol oxidase. However, other enzymes characteristic for methylotrophic growth conditions are absent or present at low levels. Most of the alcohol oxidase occurs in the octameric state and immuno-and cytochemical evidence shows that it is located in a single enlarged peroxisome per cell. Such peroxisomes show crystalloid inclusions which are lacking in the peroxisomes present in glucose grown control cells.Our results suggest that import into peroxisomes of H. polymorpha, assembly and activation of alcohol oxidase is not conditionally dependent on adaptation to methylotrophic growth conditions and that proliferation of peroxisomes is a well-programmed process that is not triggered solely by overproduction of a peroxisomal protein.LIKARYOTIC cells contain a number of membrane-enclosed compartments each devoted to carry out specific metabolic functions. To this purpose each organelle possesses its own characteristic group of enzymes and proteins. Some of these organeUes have been favorite objects of research and much is already known about their contribution to cellular metabolism and biogenesis. Relatively little is known however, about peroxisomes, which were first discovered by De Duve et al. (1966). Although rather variable in enzymatic repertoire depending on the organism or tissue in which they occur, a common feature is the presence of an H202 producing oxidase and catalase. Recent studies have revealed that peroxisomal proteins, including integral membrane proteins, are encoded in the nucleus, synthesized on free polysomes and imported posttranslationally into the organelle (reviewed by Lazarow and Fujiki, 1985). Moreover, the majority of peroxisomal proteins are synthesized at their mature size and translocation across the peroxisomal membrane occurs without any detectable modification of the protein (reviewed by Borst, 1986).A very interesting example of peroxisomal function and development is represented by methylotrophic yeasts. In these fungi the number of organelles and their physiological function is entirely dependent upon environmental conditions (for reviews see Veenhuis et al., 1983 and. For instance when the methylotrophic yeast Hansenula polymorpha is grown on methanol the cells contain a large number of peroxisomes which have a crystalline matrix exclusively composed of alcohol oxidase (AO)~ molecules (Veenhuis et al., 1978;Veenhuis et al., 1981). AO functions as the first enzyme in methanol metabolism converting methanol to formaldehyde and H202. Besides AO considerable amounts of catalase and dihydroxy acetone synthase are present in these organelles (Douma et al., 1985;Goodman, 1985)....
Alcohol oxidase (AO) expressed in transformed oleic acid‐grown Saccharomyces cerevisiae, accumulated into microbodies to up to 8% of the total protein content of the organelles. This led to a small increase in volume fraction of the organelles, but not in their number. Most of the AO protein was present in large aggregates in the cytosol. The AO synthesized was inactive, irrespective of its subcellular localization and did not contain FAD. When the same AO gene was expressed in fused protoplasts of transformed S. cerevisiae and Hansenula polymorpha, the enzyme was properly assembled and activated in H. polymorpha microbodies.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.