RESUMEN
Malignant gliomas (MGs) are the most common malignant primary brain tumors with a short life estimate accompanied by a marked reduction in the quality of life. Herpes Simplex virus-1 thymidine kinase ganciclovir (HSV-TK/GCV) system is the best characterized enzyme prodrug therapy in use. However, lipophobicity of GCV and low enzymatic activity of HSV-TK reduce the treatment efficacy. Tomato TK (ToTK) has shown high activity in combination with its specific substrate azidothymidine (AZT). The aim of this study was to evaluate whether ToTK/AZT could be used as an alternative to HSV-TK/GCV therapy. Both treatments demonstrated cytotoxicity in human MG cells in vitro. In vivo, both treatments decreased tumor growth and tumors were smaller in comparison with controls in mouse orthotopic MG model. Survival of ToTK/AZT-treated mice was significantly increased compared with control mice (*P<0.05) but not as compared with HSV-TK/GCV-treated mice. No significant differences were observed in clinical chemistry safety analyses. We conclude that both treatments showed a beneficial treatment response in comparison to controls on tumor growth and ToTK/AZT also on survival. There were no significant differences between these treatments. Therefore ToTK/AZT could be considered as an alternative treatment option for MG because of its favorable therapeutic characteristics.
Asunto(s)
Neoplasias Encefálicas/tratamiento farmacológico , Glioma/tratamiento farmacológico , Proteínas de Plantas/genética , Solanum lycopersicum/enzimología , Timidina Quinasa/genética , Animales , Antineoplásicos/farmacocinética , Antineoplásicos/uso terapéutico , Neoplasias Encefálicas/patología , Línea Celular Tumoral , Genes Transgénicos Suicidas , Terapia Genética , Glioma/patología , Herpesvirus Humano 1/enzimología , Humanos , Masculino , Ratones Desnudos , Ratas , Carga Tumoral , Ensayos Antitumor por Modelo de Xenoinjerto , Zidovudina/farmacocinética , Zidovudina/uso terapéuticoRESUMEN
A promising suicide gene therapy system to treat gliomas has been reported: the thymidine kinase 1 from tomato (toTK1) combined with the nucleoside analog pro-drug zidovudine (azidothymidine, AZT), which is known to penetrate the blood-brain barrier. Transduction with toTK1 has been found to efficiently increase the sensitivity of human glioblastoma cells to AZT, and nude rats with intracranial glioblastoma grafts have shown significantly improved survival when treated with the toTK1/AZT system. We show in our paper that the strong suicidal effect of AZT together with toTK1 may be explained by reduced TTP-mediated feedback inhibition of the AZT phosphorylation.
Asunto(s)
Inhibidores Enzimáticos/farmacología , Retroalimentación Fisiológica/efectos de los fármacos , Solanum lycopersicum/enzimología , Timidina Quinasa/antagonistas & inhibidores , Nucleótidos de Timina/farmacología , Relación Dosis-Respuesta a Droga , Humanos , Fosforilación/efectos de los fármacos , Timidina Quinasa/metabolismo , Zidovudina/metabolismoRESUMEN
We overexpressed and purified enzymes involved in the pyrimidine catabolic pathway in the yeast Saccharomyces (Lachancea) kluyveri. A new vector was therefore designed, providing the first specific expression system in Saccharomyces kluyveri. The URC1 gene was overexpressed and a soluble protein obtained and successfully purified using the C-terminally added His-tag. Our system will be used for further studies of the structure and function of the enzymes belonging to the URC pyrimidine degradation pathway.
Asunto(s)
Enzimas/biosíntesis , Proteínas Fúngicas/biosíntesis , Vectores Genéticos/genética , Biología Molecular/métodos , Saccharomyces/enzimología , Secuencia de Bases , Electroforesis en Gel de Poliacrilamida , Datos de Secuencia MolecularRESUMEN
In the Pasteurella multocida genome only one putative deoxyribonucleoside kinase encoding gene, for thymidine kinase 1 (PmTK1), was identified. The PmTK1 gene was sub-cloned into Escherichia coli KY895 and it sensitized the host towards 2',2'-difluoro-deoxycytidine (gemcitabine, dFdC), 3'-azido-thymidine (AZT) and 5-fluoro-deoxyuridine (5F-dU). PmTK1 was over-expressed and purified with two different tags. Apparently, deoxyuridine (dU), and not thymidine (dT), is the preferred substrate. We suggest that PmTK1s could be employed as a species-specific activator of uracil-based nucleoside antibiotics.
Asunto(s)
Pasteurella multocida/enzimología , Nucleósidos de Pirimidina/metabolismo , Timidina Quinasa/metabolismo , Antimetabolitos Antineoplásicos/metabolismo , Antimetabolitos Antineoplásicos/farmacología , Desoxicitidina/análogos & derivados , Desoxicitidina/metabolismo , Desoxicitidina/farmacología , Desoxiuridina/farmacología , Escherichia coli/efectos de los fármacos , Escherichia coli/genética , Escherichia coli/metabolismo , Pruebas de Sensibilidad Microbiana , Nucleósidos de Pirimidina/farmacología , Timidina Quinasa/genética , Zidovudina/farmacología , GemcitabinaRESUMEN
Yeast Saccharomyces (Lachancea) kluyveri urc4 mutants, unable to grow on uracil, biotransformed (14)C(2)-uracil into two labeled compounds, as detected by high performance liquid chromatography (HPLC). These two compounds could also be obtained following organic synthesis of ribosylurea. This finding demonstrates that in the URC pyrimidine degradation pathway, the opening of the uracil ring takes place when uracil is attached to the ribose moiety. Ribosylurea has not been reported in the cell metabolism before and the two observed compounds likely represent an equilibrium mixture of the pyranosyl and furanosyl forms.
Asunto(s)
Proteínas Fúngicas/metabolismo , Saccharomyces/genética , Saccharomyces/metabolismo , Uracilo/metabolismo , Cromatografía Líquida de Alta Presión , Proteínas Fúngicas/genética , Mutación , Ribosa/química , Ribosa/metabolismo , Uracilo/química , Urea/química , Urea/metabolismoRESUMEN
Four Clostridium perfringens phosphorylases were subcloned, overexpressed and analyzed for their substrate specificity. DeoD(1) and PunA could use a variety of purine substrates, including an antiviral drug 2',3'-dideoxyinosine (ddI). In one-pot synthesis using Clostridium phosphorylases, 2',3'-dideoxyuridine and hypoxanthine were converted to ddI at yield of about 30%.
Asunto(s)
Clostridium perfringens/enzimología , Didanosina/metabolismo , Pentosiltransferasa/metabolismo , Cromatografía Líquida de Alta Presión , Didanosina/síntesis químicaRESUMEN
High detection efficiency combined with spatial resolution on a nm-scale makes the field ionization process a promising candidate for spatially resolved neutral particles detection. The effective cross-sectional area sigma(eff) can serve as a measure for the effectiveness of such a field ion detector. In the present contribution, we combine quantum-mechanical calculations of the field-modified electron density distribution near the tungsten tip surface and of the resulting local field distributions, performed using the functional integration method, with a classical treatment of the atom trajectories approaching the tip in order to calculate the sigma(eff) values for ionization of free He atoms over an apex of a tungsten field emitter tip. The calculated values are compared with experimental data for supersonic He atomic beams at two different temperatures 95 and 298K.
RESUMEN
Beta-alanine is an intermediate in the reductive degradation of uracil. Recently we have identified and characterized the Saccharomyces kluyveri PYD4 gene and the corresponding enzyme beta -alanine aminotransferase ((Sk)Pyd4p), highly homologous to eukaryotic gamma-aminobutyrate aminotransferase (GABA-AT). S. kluyveri has two aminotransferases, GABA aminotransferase ((Sk)Uga1p) with 80% and (Sk)Pyd4p with 55% identity to S. cerevisiae GABA-AT. (Sk)Pyd4p is a typical pyridoxal phosphate-dependent aminotransferase, specific for alpha-ketoglutarate (alpha KG), beta-alanine (BAL) and gamma-aminobutyrate (GABA), showing a ping-pong kinetic mechanism involving two half-reactions and substrate inhibition. (Sk)Uga1p accepts only alpha KG and GABA but not BAL, thus only (Sk)Pydy4p belongs to the uracil degradative pathway.
Asunto(s)
Pirimidinas/metabolismo , Saccharomyces/metabolismo , beta-Alanina/metabolismo , 4-Aminobutirato Transaminasa/metabolismo , Aminación , D-Alanina Transaminasa/metabolismo , Cinética , Saccharomyces/enzimología , Análisis de Secuencia de ADN , Ácido gamma-Aminobutírico/metabolismoRESUMEN
Transduced deoxyribonucleoside kinases (dNK) can be used to kill recipient cells in combination with nucleoside prodrugs. The Drosophila melanogaster multisubstrate dNK (Dm-dNK) displays a superior turnover rate and has a great plasticity regarding its substrates. We used directed evolution to create Dm-dNK mutants with increased specificity for several nucleoside analogs (NAs) used as anticancer or antiviral drugs. Four mutants were characterized for the ability to sensitize Escherichia coli toward analogs and for their substrate specificity and kinetic parameters. The mutants had a reduced ability to phosphorylate pyrimidines, while the ability to phosphorylate purine analogs was relatively similar to the wild-type enzyme. We selected two mutants, for expression in the osteosarcoma 143B, the glioblastoma U-87M-G and the breast cancer MCF7 cell lines. The sensitivities of the transduced cell lines in the presence of the NAs fludarabine (F-AraA), cladribine (CdA), vidarabine and cytarabine were compared to the parental cell lines. The sensitivity of 143B cells was increased by 470-fold in the presence of CdA and of U-87M-G cells by 435-fold in the presence of F-AraA. We also show that a choice of the selection and screening system plays a crucial role when optimizing suicide genes by directed evolution.
Asunto(s)
Antimetabolitos , Drosophila melanogaster/enzimología , Terapia Genética/métodos , Mutación , Neoplasias/terapia , Fosfotransferasas (Aceptor de Grupo Alcohol)/genética , Animales , Antineoplásicos/uso terapéutico , Línea Celular Tumoral , Cladribina/uso terapéutico , Citarabina/uso terapéutico , Evolución Molecular Dirigida/métodos , Genes Transgénicos Suicidas , Glioblastoma/terapia , Humanos , Dosificación Letal Mediana , Osteosarcoma/terapia , Fosforilación , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Purinas/metabolismo , Especificidad por Sustrato , Transducción Genética/métodos , Vidarabina/análogos & derivados , Vidarabina/uso terapéuticoRESUMEN
The pyrimidine catabolic pathway is of crucial importance in cancer patients because it is involved in degradation of several chemotherapeutic drugs, such as 5-fluorouracil; it also is important in plants, unicellular eukaryotes, and bacteria for the degradation of pyrimidine-based biocides/antibiotics. During the last decade we have developed a yeast species, Saccharomyces kluyveri, as a model and tool to study the genes and enzymes of the pyrimidine catabolic pathway. In this report, we studied degradation of uracil and its putative degradation products in 38 yeasts and showed that this pathway was present in the ancient yeasts but was lost approximately 100 million years ago in the S. cerevisiae lineage.
Asunto(s)
Antineoplásicos/farmacología , Ensayos de Selección de Medicamentos Antitumorales , Pirimidinas/química , Evolución Molecular , Fluorouracilo/farmacología , Proteínas Fúngicas/química , Regulación Fúngica de la Expresión Génica , Genes Fúngicos , Genoma Fúngico , Modelos Genéticos , Filogenia , Saccharomyces/metabolismo , Factores de Tiempo , Uracilo/química , Uracilo/metabolismoRESUMEN
Thymidine kinases (TKs) appear to be almost ubiquitous and are found in nearly all prokaryotes, eukaryotes, and several viruses. They are the key enzymes in thymidine salvage and activation of several anti-cancer and antiviral drugs. We show that bacterial TKs can be subdivided into 2 groups. The TKs from Gram-positive bacteria are more closely related to the eukaryotic TK1 enzymes than are TKs from Gram-negative bacteria.
Asunto(s)
Bacterias/enzimología , Regulación Bacteriana de la Expresión Génica , Fosfotransferasas (Aceptor de Grupo Alcohol)/biosíntesis , Timidina Quinasa/biosíntesis , Secuencia de Aminoácidos , Evolución Molecular , Humanos , Modelos Moleculares , Datos de Secuencia Molecular , Nucleósidos/química , Sistemas de Lectura Abierta , Fosfotransferasas (Aceptor de Grupo Alcohol)/química , Filogenia , Pirimidinas/química , Homología de Secuencia de Aminoácido , Especificidad de la Especie , Timidina Quinasa/químicaRESUMEN
Twenty-six fully sequenced archaeal genomes were searched for genes coding for putative deoxyribonucleoside kinases (dNKs). We identified only 5 human-like thymidine kinase 1 genes (TK1s) and none for non-TK1 kinases. Four TK1s were identified in the Euryarchaea and one was found in the Crenarchaea, while none was found in Nanoarchaeum. The identified TK1s have high identity to Gram-positive bacteria TK1s. The TK1s from archaea, Gram-positive bacteria and eukaryotes share the same common ancestor, while the TK1s from Gram-negative bacteria belong to a less-related subgroup. It seems that a functional deoxyribonucleoside salvage pathway is not crucial for the archaeal cell.
Asunto(s)
Archaea/enzimología , Proteínas Arqueales/química , Regulación de la Expresión Génica , Timidina Quinasa/biosíntesis , Secuencia de Aminoácidos , Animales , Proteínas Bacterianas/química , Bases de Datos Genéticas , Evolución Molecular , Humanos , Datos de Secuencia Molecular , Fosfotransferasas (Aceptor de Grupo Alcohol)/química , Filogenia , Especificidad de la EspecieRESUMEN
The ability to propagate under anaerobic conditions is an essential and unique trait of brewer's or baker's yeast ( Saccharomyces cervisiae). To understand the evolution of facultative anaerobiosis we studied the dependence of de novo pyrimidine biosynthesis, more precisely the fourth enzymic activity catalysed by dihydroorotate dehydrogenase (DHODase), on the enzymes of the respiratory chain in several yeast species. While the majority of yeasts possess a mitochondrial DHODase, Saccharomyces cerevisiae has a cytoplasmatic enzyme, whose activity is independent of the presence of oxygen. From the phylogenetic point of view, this enzyme is closely related to a bacterial DHODase from Lactococcus lactis. Here we show that S. kluyveri, which separated from the S. cerevisiae lineage more than 100 million years ago, represents an evolutionary intermediate, having both cytoplasmic and mitochondrial DHODases. We show that these two S. kluyveri enzymes, and their coding genes, differ in their dependence on the presence of oxygen. Only the cytoplasmic DHODase promotes growth in the absence of oxygen. Apparently a Saccharomyces yeast progenitor which had a eukaryotic-like mitochondrial DHODase acquired a bacterial gene for DHODase, which subsequently allowed cell growth gradually to become independent of oxygen.
Asunto(s)
Anaerobiosis , Evolución Biológica , Transferencia de Gen Horizontal , Pirimidinas/biosíntesis , Saccharomyces cerevisiae/enzimología , Saccharomyces cerevisiae/crecimiento & desarrollo , División Celular , Citoplasma/enzimología , ADN de Hongos/genética , ADN de Hongos/aislamiento & purificación , Dihidroorotato Deshidrogenasa , Transporte de Electrón , Mitocondrias/enzimología , Oxidorreductasas actuantes sobre Donantes de Grupo CH-CH/metabolismo , Oxígeno/metabolismo , Filogenia , Saccharomyces cerevisiae/genética , Fracciones Subcelulares/enzimologíaRESUMEN
Saccharomyces kluyveri is a petite-negative yeast, which is less prone to form ethanol under aerobic conditions than is S. cerevisiae. The first reaction on the route from pyruvate to ethanol is catalysed by pyruvate decarboxylase, and the differences observed between S. kluyveri and S. cerevisiae with respect to ethanol formation under aerobic conditions could be caused by differences in the regulation of this enzyme activity. We have identified and cloned three genes encoding functional pyruvate decarboxylase enzymes (PDCgenes) from the type strain of S. kluyveri (Sk- PDC11, Sk- PDC12 and Sk- PDC13). The regulation of pyruvate decarboxylase in S. kluyveri was studied by measuring the total level of Sk- PDC mRNA and the overall enzyme activity under various growth conditions. It was found that the level of Sk- PDC mRNA was enhanced by glucose and oxygen limitation, and that the level of enzyme activity was controlled by variations in the amount of mRNA. The mRNA level and the pyruvate decarboxylase activity responded to anaerobiosis and growth on different carbon sources in essentially the same fashion as in S. cerevisiae. This indicates that the difference in ethanol formation between these two yeasts is not due to differences in the regulation of pyruvate decarboxylase(s), but rather to differences in the regulation of the TCA cycle and the respiratory machinery. However, the PDC genes of Saccharomyces/ Kluyveromyces yeasts differ in their genetic organization and phylogenetic origin. While S. cerevisiae and S. kluyveri each have three PDC genes, these have apparently arisen by independent duplications and specializations in each of the two yeast lineages.
Asunto(s)
Piruvato Descarboxilasa/genética , Saccharomyces/clasificación , Saccharomyces/enzimología , Aerobiosis , Anaerobiosis , Eliminación de Gen , Glucosa/metabolismo , Cinética , Filogenia , Piruvato Descarboxilasa/metabolismo , Saccharomyces/genética , Saccharomyces/crecimiento & desarrolloRESUMEN
The complete sequences of mitochondrial DNA (mtDNA) from the two budding yeasts Saccharomyces castellii and Saccharomyces servazzii, consisting of 25 753 and 30 782 bp, respectively, were analysed and compared to Saccharomyces cerevisiae mtDNA. While some of the traits are very similar among Saccharomyces yeasts, others have highly diverged. The two mtDNAs are much more compact than that of S.cerevisiae and contain fewer introns and intergenic sequences, although they have almost the same coding potential. A few genes contain group I introns, but group II introns, otherwise found in S.cerevisiae mtDNA, are not present. Surprisingly, four genes (ATP6, COX2, COX3 and COB) in the mtDNA of S.servazzii contain, in total, five +1 frameshifts. mtDNAs of S.castellii, S.servazzii and S.cerevisiae contain all genes on the same strand, except for one tRNA gene. On the other hand, the gene order is very different. Several gene rearrangements have taken place upon separation of the Saccharomyces lineages, and even a part of the transcription units have not been preserved. It seems that the mechanism(s) involved in the generation of the rearrangements has had to ensure that all genes stayed encoded by the same DNA strand.
Asunto(s)
ADN Mitocondrial/genética , Saccharomyces/genética , Secuencia de Bases , ADN Intergénico , ADN Mitocondrial/química , Endodesoxirribonucleasas/metabolismo , Endorribonucleasas/genética , Orden Génico , Genes de ARNr , Intrones , Proteínas Mitocondriales/genética , Datos de Secuencia Molecular , Sistemas de Lectura Abierta , ARN/química , ARN/metabolismo , ARN Catalítico/genética , ARN Mitocondrial , ARN de Transferencia/genética , Secuencias Repetitivas de Ácidos Nucleicos , Ribonucleasa P , Saccharomyces cerevisiae/genética , Análisis de Secuencia de ADN , Especificidad de la Especie , Sitio de Iniciación de la Transcripción , Transcripción GenéticaRESUMEN
In order to evaluate the potential of Saccharomyces kluyveri for heterologous protein production, S. kluyveri Y159 was transformed with a S. cerevisiae-based multi-copy plasmid containing the S. cerevisiae PEP4 gene, which encodes proteinase A, under the control of its native promoter. As a reference, S. cerevisiae CEN.PK 113-5D was transformed with the same plasmid and the two strains were characterised in batch cultivations on glucose. The glucose metabolism was found to be less fermentative in S. kluyveri than in S. cerevisiae. The yield of ethanol on glucose was 0.11 g/g in S. kluyveri, compared to a yield of 0.40 g/g in S. cerevisiae. Overexpression of PEP4 led to the secretion of active proteinase A in both S. kluyveri and S. cerevisiae. The yield of active proteinase A during growth on glucose was found to be 3.6-fold higher in S. kluyveri than in the S. cerevisiae reference strain.
Asunto(s)
Ácido Aspártico Endopeptidasas/biosíntesis , Saccharomyces/metabolismo , Etanol/metabolismo , Glucosa/metabolismo , Plásmidos , Regiones Promotoras Genéticas , Saccharomyces/genéticaRESUMEN
beta-Alanine synthase (EC 3.5.1.6), which catalyzes the final step of pyrimidine catabolism, has only been characterized in mammals. A Saccharomyces kluyveri pyd3 mutant that is unable to grow on N-carbamyl-beta-alanine as the sole nitrogen source and exhibits diminished beta-alanine synthase activity was used to clone analogous genes from different eukaryotes. Putative PYD3 sequences from the yeast S. kluyveri, the slime mold Dictyostelium discoideum, and the fruit fly Drosophila melanogaster complemented the pyd3 defect. When the S. kluyveri PYD3 gene was expressed in S. cerevisiae, which has no pyrimidine catabolic pathway, it enabled growth on N-carbamyl-beta-alanine as the sole nitrogen source. The D. discoideum and D. melanogaster PYD3 gene products are similar to mammalian beta-alanine synthases. In contrast, the S. kluyveri protein is quite different from these and more similar to bacterial N-carbamyl amidohydrolases. All three beta-alanine synthases are to some degree related to various aspartate transcarbamylases, which catalyze the second step of the de novo pyrimidine biosynthetic pathway. PYD3 expression in yeast seems to be inducible by dihydrouracil and N-carbamyl-beta-alanine, but not by uracil. This work establishes S. kluyveri as a model organism for studying pyrimidine degradation and beta-alanine production in eukaryotes.
Asunto(s)
Amidohidrolasas/metabolismo , Amidohidrolasas/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Clonación Molecular , Dictyostelium/enzimología , Drosophila melanogaster/enzimología , Regulación Fúngica de la Expresión Génica , Genes Fúngicos , Datos de Secuencia Molecular , Conformación Proteica , ARN Mensajero/genética , Saccharomyces/enzimología , Saccharomyces/genética , Saccharomyces/crecimiento & desarrollo , Homología de Secuencia de AminoácidoRESUMEN
Deoxyribonucleoside kinases phosphorylate deoxyribonucleosides and activate a number of medically important nucleoside analogs. Here we report the structure of the Drosophila deoxyribonucleoside kinase with deoxycytidine bound at the nucleoside binding site and that of the human deoxyguanosine kinase with ATP at the nucleoside substrate binding site. Compared to the human kinase, the Drosophila kinase has a wider substrate cleft, which may be responsible for the broad substrate specificity of this enzyme. The human deoxyguanosine kinase is highly specific for purine substrates; this is apparently due to the presence of Arg 118, which provides favorable hydrogen bonding interactions with the substrate. The two new structures provide an explanation for the substrate specificity of cellular deoxyribonucleoside kinases.
Asunto(s)
Adenosina Trifosfato/metabolismo , Desoxicitidina/metabolismo , Drosophila melanogaster/enzimología , Fosfotransferasas (Aceptor de Grupo Alcohol)/química , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Secuencia de Aminoácidos , Animales , Sitios de Unión , Cristalografía por Rayos X , Humanos , Enlace de Hidrógeno , Modelos Moleculares , Datos de Secuencia Molecular , Conformación Proteica , Alineación de Secuencia , Relación Estructura-Actividad , Especificidad por SustratoRESUMEN
The genome of Saccharomyces cerevisiae contains several duplicated regions. The recent sequencing results of several yeast species suggest that the duplicated regions found in the modern Saccharomyces species are probably the result of a single gross duplication, as well as a series of sporadic independent short-segment duplications. The gross duplication might coincide with the origin of the ability to grow under anaerobic conditions.
Asunto(s)
Cromosomas Fúngicos , Genes Duplicados , Genoma Fúngico , Saccharomyces cerevisiae/genética , Animales , Modelos Genéticos , Filogenia , Saccharomyces cerevisiae/clasificaciónRESUMEN
Saccharomyces cerevisiae is a petite-phenotype-positive ("petite-positive") yeast, which can successfully grow in the absence of oxygen. On the other hand, Kluyveromyces lactis as well as many other yeasts are petite negative and cannot grow anaerobically. In this paper, we show that Saccharomyces kluyveri can grow under anaerobic conditions, but while it can generate respiration-deficient mutants, it cannot generate true petite mutants. From a phylogenetic point of view, S. kluyveri is apparently more closely related to S. cerevisiae than to K. lactis. These observations suggest that the progenitor of the modern Saccharomyces and Kluyveromyces yeasts, as well as other related genera, was a petite-negative and aerobic yeast. Upon separation of the K. lactis and S. kluyveri-S. cerevisiae lineages, the latter developed the ability to grow anaerobically. However, while the S. kluyveri lineage has remained petite negative, the lineage leading to the modern Saccharomyces sensu stricto and sensu lato yeasts has developed the petite-positive characteristic.