A new isolate, Gordonia sp. strain TY-5, is capable of growth on propane and n-alkanes with C 13 to C 22 carbon chains as the sole source of carbon. In whole-cell reactions, significant propane oxidation to 2-propanol was detected. A gene cluster designated prmABCD, which encodes the components of a putative dinucleariron-containing multicomponent monooxygenase, including the large and small subunits of the hydroxylase, an NADH-dependent acceptor oxidoreductase, and a coupling protein, was cloned and sequenced. A mutant with prmB disrupted (prmB::Kan r ) lost the ability to grow on propane, and Northern blot analysis revealed that polycistronic transcription of the prm genes was induced during its growth on propane. These results indicate that the prmABCD gene products play an essential role in propane oxidation by the bacterium. Downstream of the prm genes, an open reading frame (adh1) encoding an NAD ؉ -dependent secondary alcohol dehydrogenase was identified, and the protein was purified and characterized. The Northern blot analysis results and growth properties of a disrupted mutant (adh1::Kan r ) indicate that Adh1 plays a major role in propane metabolism. Two additional NAD ؉ -dependent secondary alcohol dehydrogenases (Adh2 and Adh3) were also found to be involved in 2-propanol oxidation. On the basis of these results, we conclude that Gordonia sp. strain TY-5 oxidizes propane by monooxygenase-mediated subterminal oxidation via 2-propanol.Gaseous n-alkanes ranging from C 2 to C 5 are recognized as components of nonmethane hydrocarbons, and the increased concentrations of these gases in the atmosphere threaten to destabilize ecosystems through a variety of mechanisms (48). Although these gases are produced as natural intermediates of bacterial, plant, and mammalian metabolism, the main sources of pollution are natural oil seepage and oil spills (42). From a biotechnological perspective, gaseous alkanes are inexpensive carbon sources for microbial cultivation, and the enzymes participating in the oxidation pathway promise to be versatile biocatalysts.A number of microorganisms have been isolated for their ability to use gaseous n-alkanes as a sole carbon source. In the case of bacteria, these abilities have been found in some Pseudomonas strains (57) and many strains belonging to the order Actinomycetales, such as those of the genera Rhodococcus, Mycobacterium, Corynebacterium, Nocardia, and Pseudonocardia (3,15). Some of the bacteria are known to degrade various environmental pollutants (trichloroethylene, chloroform, methyl ethers, etc.) through cometabolism with gaseous alkanes (13, 52).The pathways for the oxidation of gaseous alkanes have received little attention compared with those for the microbial oxidation of methane (34) and liquid n-alkanes (24). Recently, the terminal oxidation pathway of butane (butane 3 1-butanol 3 butyraldehyde 3 butyrate) by "Pseudomonas butanovora" has been confirmed through enzymological and genetic approaches (2, 14). The first reaction is catalyzed by a soluble butane m...

The capacity to use methanol as sole source of carbon and energy is restricted to relatively few yeast species. This may be related to the low efficiency of methanol metabolism in yeast, relative to that of prokaryotes. This contribution describes the details of methanol metabolism in yeast and focuses on the significance of compartmentalization of this metabolic pathway in peroxisomes.

Methanol is a valuable raw material used in the manufacture of useful chemicals as well as a potential source of energy to replace coal and petroleum. Biotechnological interest in the microbial utilization of methanol has increased because it is an ideal carbon source and can be produced from renewable biomass. Formaldehyde, a cytotoxic compound, is a central metabolic intermediate in methanol metabolism. Therefore, microorganisms utilizing methanol have adopted several metabolic strategies to cope with the toxicity of formaldehyde. Formaldehyde is initially detoxified through trapping by some cofactors, such as glutathione, mycothiol, tetrahydrofolate, and tetrahydromethanopterin, before being oxidized to CO2. Alternatively, free formaldehyde can be trapped by sugar phosphates as the first reaction in the C1 assimilation pathways: the xylulose monophosphate pathway for yeasts and the ribulose monophosphate (RuMP) pathway for bacteria. In yeasts, although formaldehyde generation and consumption takes place in the peroxisome, the cytosolic formaldehyde oxidation pathway also plays a role in formaldehyde detoxification as well as energy formation. The key enzymes of the RuMP pathway are found in a variety of microorganisms including bacteria and archaea. Regulation of the genes encoding these enzymes and their catalytic mechanisms depend on the physiological traits of these organisms during evolution.

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Reactive oxygen species are generated within peroxisomes during peroxisomal metabolism. However, due to technological difficulties, the intraperoxisomal redox state remain elusive, and the effect of peroxisome deficiency on the intracellular redox state is controversial. A newly developed, genetically encoded fluorescence resonance energy transfer (FRET) probe, Redoxfluor, senses the physiological redox state via its internal disulfide bonds, resulting in a change in the conformation of the protein leading to a FRET response. We made use of Redoxfluor to measure the redox states at the subcellular level in yeast and Chinese hamster ovary (CHO) cells. In wild-type peroxisomes harboring an intact fatty acid ␤-oxidation system, the redox state within the peroxisomes was more reductive than that in the cytosol, despite the fact that reactive oxygen species were generated within the peroxisomes. Interestingly, we observed that the redox state of the cytosol of cell mutants for peroxisome assembly, regarded as models for a neurological metabolic disorder, was more reductive than that of the wild-type cells in yeast and CHO cells. Furthermore, Redoxfluor was utilized to develop an efficient system for the screening of drugs that moderate the abnormal cytosolic redox state in the mutant CHO cell lines for peroxisome assembly without affecting the redox state of normal cells.

Eukaryotic methylotrophs, which are able to obtain all the carbon and energy needed for growth from methanol, are restricted to a limited number of yeast species. When these yeasts are grown on methanol as the sole carbon and energy source, the enzymes involved in methanol metabolism are strongly induced, and the membrane-bound organelles, peroxisomes, which contain key enzymes of methanol metabolism, proliferate massively. These features have made methylotrophic yeasts attractive hosts for the production of heterologous proteins and useful model organisms for the study of peroxisome biogenesis and degradation. In this paper, we describe recent insights into the molecular basis of yeast methylotrophy.

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A newly isolated denitrifying bacterium, Thauera sp. strain DNT-1, grew on toluene as the sole carbon and energy source under both aerobic and anaerobic conditions. When this strain was cultivated under oxygenlimiting conditions with nitrate, first toluene was degraded as oxygen was consumed, while later toluene was degraded as nitrate was reduced. Biochemical observations indicated that initial degradation of toluene occurred through a dioxygenase-mediated pathway and the benzylsuccinate pathway under aerobic and denitrifying conditions, respectively. Homologous genes for toluene dioxygenase (tod) and benzylsuccinate synthase (bss), which are the key enzymes in aerobic and anaerobic toluene degradation, respectively, were cloned from genomic DNA of strain DNT-1. The results of Northern blot analyses and real-time quantitative reverse transcriptase PCR suggested that transcription of both sets of genes was induced by toluene. In addition, the tod genes were induced under aerobic conditions, whereas the bss genes were induced under both aerobic and anaerobic conditions. On the basis of these results, it is concluded that strain DNT-1 modulates the expression of two different initial pathways of toluene degradation according to the availability of oxygen in the environment.Benzene, toluene, ethylbenzene, and xylenes (BTEX) are one of the most common groups of groundwater contaminants. Of these contaminants, toluene is degraded by many strains of aerobic bacteria, and five different aerobic toluene degradation pathways have been identified. Burkholderia cepacia G4, Ralstonia pickettii PKO1, and Pseudomonas mendocina KR1 first oxidize toluene using specific monooxygenases to form o-, m-, and p-cresol, respectively (34, 35, 52). The cresols formed by strains G4 and PKO1 undergo a second monooxygenation to form 3-methylcatechol, which is then degraded by a meta ring fission pathway (35,45). In strain KR1, the methyl group of p-cresol is oxidized, and the resulting 4-hydroxybenzoate is degraded by an ortho cleavage pathway (51). On the other hand, Pseudomonas putida mt-2 oxidizes the methyl group of toluene to form benzoic acid, which is further metabolized through a meta cleavage pathway via catechol (4). P. putida F1 carries the chromosomally encoded tod pathway. Toluene dioxygenase (TodC1C2BA) oxidizes toluene to cis-toluene dihydrodiol. Then, toluene dihydrodiol dehydrogenase (TodD) transforms the dihydrodiol to 3-methylcatechol, which is cleaved by the meta fission enzyme 3-methylcatechol 2,3-