980 resultados para Purinergic P1


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Aliar boa qualidade de grãos às variedades com alto rendimento, ciclo curto e adaptação é um dos objetivos dos programas de melhoramento de aveia no sul do Brasil. O peso dos grãos tem sido um dos critérios utilizados para determinar essa qualidade; porém, para melhor manipular o peso dos grãos nos programas de melhoramento, é necessário o estudo de suas bases genéticas em germoplasma adaptado de aveia. Este trabalho foi realizado com o objetivo de estudar a herança dos caracteres peso de grãos primários e secundários da aveia. Para isso, foram pesadas amostras de 20 grãos primários e secundários de um número variável de plantas nas gerações P1, P2, F1, F2 e F3 de cinco cruzamentos de aveia. Com esses dados, foram obtidas as distribuições de freqüência, variâncias, os efeitos gênicos predominantes, e estimados os valores de herdabilidade no sentido amplo, e usando regressão genitor-progênie. Os resultados mostraram que existe variabilidade em progênies precoces no peso de grãos primários e secundários, e que aditividade e dominância são os efeitos gênicos atuantes. Não foi detectada a presença de genes maiores para a expressão dessas características. Além disso, variações contínuas em F2 e herdabilidades baixas a moderadas indicam que seleção amena pode ser aplicada em gerações iniciais.

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Autosomal dominant familial dysalbuminemic hyperthyroxinemia (FDH)is characterized by modified human serum albumin (HSA) inducing asubstantially higher affinity for thyroxine (T4). Histidin or prolinsubstitution on residue R218 produces localized conformationalchanges of HSA creating additional room for T4 binding, leadingto 14-20 fold normal total T4 (TT4) levels. Affected individuals areconsidered euthyroid. Our patient is an 18 months-old swiss girl bornto a mother known for the rare R218P mutation in the HSA gene.She presented with severe failure to thrive (height -2.92 SD, weight-3.6 SD), habitual hip dislocation without anatomical anomaly, latefontanelle closing and protruding ears. Psychomotor development isslightly retarded. Thyroid function testing confirmed extremely high TT4(1446.0 nmol/l) levels, which are similar to her brother's values (1534.4nmol/l and 1757.6 nmol/l respectively). Free T4 seems slightly elevated(26 pmol/l), probably due to methodological reasons. TSH (0.92 mU/l),free T3 (4.4 pmol/l) and thyroxin binding globulin (32 mg/l) are withinthe normal range. Her two half-brothers, affected by the samemutation, are now 18.7 (P1) and 16.6 (P2) years old and wereoriginally described by S. Pannain et al. in 2000. Both werecharacterized by growth retardation (-2.1 and -2.2 SD) before the ageof 4 years. P1 has reached a normal adult height (-0.4 SD) and P2has caught up to normal growth (-0.68 SD) with moderate bonematuration delay. Pubertal development and anterior pituitary functionare adequate. Primary growth and developmental retardation in thefirst years of life with adequate catch-up seem to be a distinctcharacteristic in FDH with R218P mutation. Hip dislocation is typicallyseen in other situations associated to thyroid disorders, like Downsyndrome. These findings might be explained by altered early thyroidhormone utilization in children with FDH.

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The IncP alpha promiscuous plasmid (R18, R68, RK2, RP1 and RP4) comprises 60,099 bp of nucleotide sequence, encoding at least 74 genes. About 40 kb of the genome, designated the IncP core and including all essential replication and transfer functions, can be aligned with equivalent sequences in the IncP beta plasmid R751. The compiled IncP alpha sequence revealed several previously unidentified reading frames that are potential genes. IncP alpha plasmids carry genetic information very efficiently: the coding sequences of the genes are closely packed but rarely overlap, and occupy almost 86% of the genome's nucleotide sequence. All of the 74 genes should be expressed, although there is as yet experimental evidence for expression of only 60 of them. Six examples of tandem-in-frame initiation sites specifying two gene products each are known. Two overlapping gene arrangements occupy different reading frames of the same region. Intergenic regions include most of the 25 promoters; transcripts are usually polycistronic. Translation of most of the open reading frames seems to be initiated independently, each from its own ribosomal binding and initiation site, although, a few cases of coupled translation have been reported. The most frequently used initiation codon is AUG but translation for a few open reading frames begins at GUG or UUG. The most common stop-codon is UGA followed by UAA and then UAG. Regulatory circuits are complex and largely dependent on two components of the central control operon. KorA and KorB are transcriptional repressors controlling at least seven operons. KorA and KorB act synergistically in several cases by recognizing and binding to conserved nucleotide sequences. Twelve KorB binding sites were found around the IncP alpha sequence and these are conserved in R751 (IncP beta) with respect to both sequence and location. Replication of IncP alpha plasmids requires oriV and the plasmid-encoded initiator protein TrfA in combination with the host-encoded replication machinery. Conjugative plasmid transfer depends on two separate regions occupying about half of the genome. The primary segregational stability system designated Par/Mrs consists of a putative site-specific recombinase, a possible partitioning apparatus and a post-segregational lethality mechanism, all encoded in two divergent operons. Proteins related to the products of F sop and P1 par partitioning genes are separately encoded in the central control operon.

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A method for the quantitative analysis of the hydrophobicity of the mycelial mat of filamentous fungi based on contact angle measurements is presented. It was tested for a range of fungi belonging to the classes of basidiomycetes, ascomycetes and deuteromycetes. The measured contact angles of the mycelial mats ranged between hydrophilic (<30 degrees) for the deuteromycetes Fusarium oxysporum Fo47 GUS1 and Trichoderma harzianum P1[pZEGA1] and hydrophobic (>60 degrees) for the ascomycete Cladosporium sp. DSE48.1b and the basidiomycetes Paxillus involutus WSL 37.7, Hebeloma crustiliniforme WSL 6.2, Suillus bovinus WSL 48.1 and Laccaria bicolor WSL 73.1. For some fungi, variations in the hydrophobicity of the mycelium depending on the growth medium, the physiological state and the exposure to water were distinguished.

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The therapeutic efficacy of anticancer chemotherapies may depend on dendritic cells (DCs), which present antigens from dying cancer cells to prime tumor-specific interferon-gamma (IFN-gamma)-producing T lymphocytes. Here we show that dying tumor cells release ATP, which then acts on P2X(7) purinergic receptors from DCs and triggers the NOD-like receptor family, pyrin domain containing-3 protein (NLRP3)-dependent caspase-1 activation complex ('inflammasome'), allowing for the secretion of interleukin-1beta (IL-1beta). The priming of IFN-gamma-producing CD8+ T cells by dying tumor cells fails in the absence of a functional IL-1 receptor 1 and in Nlpr3-deficient (Nlrp3(-/-)) or caspase-1-deficient (Casp-1(-/-)) mice unless exogenous IL-1beta is provided. Accordingly, anticancer chemotherapy turned out to be inefficient against tumors established in purinergic receptor P2rx7(-/-) or Nlrp3(-/-) or Casp1(-/-) hosts. Anthracycline-treated individuals with breast cancer carrying a loss-of-function allele of P2RX7 developed metastatic disease more rapidly than individuals bearing the normal allele. These results indicate that the NLRP3 inflammasome links the innate and adaptive immune responses against dying tumor cells.

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Aspergillus fumigatus grows well at neutral and acidic pH in a medium containing protein as the sole nitrogen source by secreting two different sets of proteases. Neutral pH favors the secretion of neutral and alkaline endoproteases, leucine aminopeptidases (Laps) which are nonspecific monoaminopeptidases, and an X-prolyl dipeptidase (DppIV). Acidic pH environment promotes the secretion of an aspartic endoprotease of pepsin family (Pep1) and tripeptidyl-peptidases of the sedolisin family (SedB and SedD). A novel prolyl peptidase, AfuS28, was found to be secreted in both alkaline and acidic conditions. In previous studies, Laps were shown to degrade peptides from their N-terminus until an X-Pro sequence acts as a stop signal. X-Pro sequences can be then removed by DppIV, which allows Laps access to the following residues. We have shown that at acidic pH Seds degrade large peptides from their N-terminus into tripeptides until Pro in P1 or P'1 position acts as a stop for these exopeptidases. However, X-X-Pro and X-X-X-Pro sequences can be removed by AfuS28 thus allowing Seds further sequential proteolysis. In conclusion, both alkaline and acidic sets of proteases contain exoprotease activity capable of cleaving after proline residues that cannot be removed during sequential digestion by nonspecific exopeptidases.

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The objective of this work was to determine the inheritance of resistance by antixenosis in tomato plants (Lycopersicon esculentum) to tomato leafminer [Tuta absoluta (Lepidoptera: Gelechiidae)]. Evaluations were performed for tomato plants of the generations P1, P2, F1, F2, RC1 and RC2. The measured characteristic in the parents, BGH-1497 (P2 male) and 'Santa Clara' (P1 female), and in the F1, F2, RC1 and RC2 generations was the number of eggs per plant. This number was converted to the oviposition nonpreference index. The inheritance of antixenosis resistance of genotype BGH-1497 is ruled by a gene of greater effect and polygenes in epistatic interactions, with a phenotypic proportion of 13:3 between susceptible and resistant genotypes, respectively.

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The objective of this work was to assess the performance of panel clones under crowns resistant to South American leaf blight (Microcyclus ulei). The experiment was carried out with 18 panel clones crown-budded with Hevea pauciflora x H. guianensis, in a Xanthic Ferralsol (Oxisol) in Manaus, AM, Brazil. The following parameters were evaluated: dry rubber yield, plant nutritional status, and anatomical and physiological characteristics of the latex vessels. In the first three years of evaluation, the panel clones IAN 2878, IAN 2903, CNS AM 7905, CNS AM 7905 P1, and PB 28/59 showed the highest dry rubber yield potential, while the clones IAN 6158, IAN 6590, and IAN 6515 should not be recommended for crown budding. Higher potassium and copper foliar content in panel clones were associated to an increase in dry rubber yield. The simultaneous evaluation of anatomical and physiological characteristics of latex is fundamental for the selection of panel clones in the Amazon region. Crown budding is an efficient technology for South American leaf blight management in endemic regions.

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O objetivo deste trabalho foi determinar a herança da resistência à murcha de Curtobacterium em feijoeiro. Foram realizados dois experimentos: no primeiro, cinco genótipos de feijoeiro, com diferentes reações de resistência à murcha de Curtobacterium, foram cruzados em arranjo dialélico; e no segundo, dois cruzamentos entre genótipos resistentes e suscetíveis - IAC Carioca Aruã x SCS Guará e IAC Carioca Pyatã x Pérola - foram realizados para dar origem às gerações P1, P2, F1, F2, RC1 e RC2. Em ambos os experimentos, a resistência do feijoeiro à murcha bacteriana foi avaliada por meio da inoculação do isolado Cff 2634. A análise dialélica mostrou que, embora efeitos aditivos e não aditivos estejam envolvidos, houve maior participação de genes com efeito aditivo no controle genético da resistência à murcha bacteriana, o que mostra a possibilidade de se obter sucesso com a seleção. A herança da resistência à murcha de Curtobacterium é complexa, com mais de três genes envolvidos, e herdabilidade no sentido restrito de 29%, para o cruzamento 'IAC Carioca Aruã' x 'SCS Guará', e de 44%, para o cruzamento 'IAC Carioca Pyatã' x 'Pérola'.

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The objective of this work was to evaluate the effect of the pasture (Urochloa brizantha) component age on soil biological properties, in a crop-livestock integrated system. The experiment was carried out in a Brazilian savannah (Cerrado) area with 92 ha, divided into six pens of approximately 15 ha. Each pen represented a different stage of the pasture component: formation, P0; one year, P1; two years, P2; three years, P3; and final with 3.5 years, Pf. Samples were taken in the 0-10 cm soil depth. The soil biological parameters - microbial biomass carbon (MBC), microbial biomass respiration (C-CO2), metabolic quotient (qCO2), microbial quotient (q mic), and total organic carbon (TOC) - were evaluated and compared among different stages of the pasture, and between an adjacent area under native Cerrado and another area under degraded pasture (PCD). The MBC, q mic and TOC increased and qCO2 reduced under the different pasture stages. Compared to PCD, the pasture stages had higher MBC, q mic and TOC, and lower qCO2. The crop-livestock integrated system improved soil microbiological parameters and immobilized carbon in the soil in comparison to the degraded pasture.

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Introduction et But de l'étude. - La transplantation de cellules souches hématopoïétiques est un des traitements proposés dans le cadre de certaines hémopathies malignes. Elle est fréquemment associée à une anorexie, des nausées et des douleurs buccales limitant les ingesta. Chez ces patients, il a été démontré qu'une altération du statut nutritionnel était associée à une durée de séjour hospitalier augmentée. Si l'évolution hospitalière est généralement bien documentée, peu d'informations nutritionnelles sur la période post-greffe sont disponibles. L'objectif de cette étude est de documenter l'évolution pondérale en fonction des différentes phases de traitement.Matériel et Méthodes. - Cette étude rétrospective a porté sur un collectif de patients suivis par la consultation ambulatoire d'onco-hématologie. Ont été inclus tous les dossiers de patients ayant bénéficié d'une autogreffe depuis plus de 100 jours. Les variables démographiques, médicales, nutritionnelles et fonctionnelles ont été recueillies aux périodes suivantes de prise en charge : lors du diagnostic (P1), à l'admission (P2) et à la sortie de l'hôpital lors de l'autogreffe (P3) et au 100e jour post-autogreffe (P4).Résultats. - L'échantillon était composé de 22 hommes et 11 femmes, ayant une moyenne d'âge de 52 ± 11 ans, un BMI moyen de 26,7 ± 4,2 et souffrant de lymphome (49 %), myélome (45 %), maladie de Hodgkin (3 %) ou amyloïdose (3 %). La durée moyenne d'hospitalisation pour l'autogreffe est de 21 ± 4 jours. À P1 et P3, seul 1 patient présentait un BMI < 18,5, et aucun patient aux autres périodes étudiées. Un BMI supérieur à 25 kg/m2 était présent chez 64 % à P1, 67 % à P2, 45 % à P3, 48 % à P4. Trente pour cent des patients perdent plus de 5 % de leur poids entre P1 et P4 dont 80 % sont des hommes. Leur BMI moyen à P1 est de 28,8 ± 3,3 kg/m2 (10 % de normal, 60 % de surpoids et 30 % d'obésité) et à P4 de 26,7 ± 3,1 kg/m2 (30 % de normal, 60 % de surpoids et 10 % d'obésité). Ces patients ont une perte de poids de 2,4 ± 4,5 % entre P1 et P2, de 8,6 ± 4,4 % entre P1 et P3 et de 7,4 ± 1,7 % entre P1 et P4.Durant le séjour hospitalier, les patients perdent en moyenne 5,6 ± 2,9 % de leur poids d'entrée (P2). Les jours qui suivent l'autogreffe50 % des sujets perdent 6 ± 3,5 %, Durant l'hospitalisation, 33 % des patients ont reçu un support nutritionnel. La prescription d'un support nutritionnel est corrélé avec la présence de candidose (r = 0,350 ; p = 0,044).Conclusion. - La majorité de ces patients oncohématologiques traités par autogreffe de cellules souches perdent du poids pendant l'hospitalisation et ceci persiste au 100e jour post-greffe pour 21 % de l'échantillon. Le BMI est élevé au moment du diagnostic et le reste tout au long de la prise en charge. Une étude prospective sur un échantillon plus large pourrait dans le futur permettre de déterminer les facteurs prédictifs d'une perte de poids persistante 3 mois après une autogreffe.

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Summary Acquisition of lineage-specific cell cycle duration is an important feature of metazoan development. In Caenorhabditis a/egans, differences in cell cycle duration are already apparent in two-cell stage embryos, when the larger anterior blastomere AB divides before the smaller posterior blastomere P1. This time difference is under the control of anterior-posterior (A-P) polarity cues set by the PAR proteins. The mechanism by which these cues regulate the cell cycle machinery differentially in AB and P1 are incompletely understood. Previous work established that retardation of P1 cell division is due in part to preferential activation of an ATL1/CHK-1 dependent checkpoint in P1 but how the remaining time difference is controlled was not known at the onset of my work. The principal line of work in this thesis established that differential timing relies also on a mechanism that promotes mitosis onset preferentially in AB. The polo-like kinase PLK-1, a positive regulator of mitotic entry, is distributed in an asymmetric manner in two-cell stage embryos, with more protein present in AB than in P1. We find that PLK-1 asymmetry is regulated by anterior-posterior (A-P) polarity cues through preferential protein retention in the embryo anterior. Importantly, mild inactivation of plk-1 by RNAi delays entry into mitosis in P1 but not in AB, in a manner that is independent of ATL-1/CHK-1. Together, these findings favor a model in which differential timing of mitotic entry in C. elegans embryos relies on two complementary mechanisms: ATL-1/CHK-1 dependent preferential retardation in P1 and PLK-1 dependent preferential promotion in AB, which together couple polarity cues and cell cycle progression during early development. Besides analyzing PLK-1 asymmetry and its role in differential timing of two-cells stage embryos, we also characterized t2190, a mutant that exhibits reduced differential timing between AB and P1. We found this mutant to be a new allele of par-1. Additionally, we analyzed the role of NMY-2 in regulating the asynchrony of two-cell stage embryos, which may be uncoupled from its role in A-P polarity establishment and carried out a preliminary analysis of the mechanism underlying CDC-25 asymmetry between AB and P,. Overall, our works bring new insights into the mechanism controlling cell cycle progression in early C. elegans embryos. As most of the players important in C. elegans are conserved in other organisms, analogous mechanisms may be utilized in polarized cells of other species. Résumé Au cours du développement, les processus de division cellulaire sont régulés dans l'espace et le temps afin d'aboutir à la formation d'un organisme fonctionnel. Chez les Métazoaires, l'un des mécanismes de contrôle s'effectue au niveau de la durée du cycle cellulaire, celle-ci étant specifiée selon la lignée cellulaire. L'embryon du nématode Caenorhabditis elegans apparaît comme un excellent modèle d'étude de la régulation temporelle du cycle cellulaire. En effet, suite à la première division du zygote, l'embryon est alors composé de deux cellules de taille et d'identité différentes, appelées blastomères AB et P1. Ces deux cellules vont ensuite se diviser de manière asynchrone, le grand blastomère antérieur AB se divisant plus rapidement que le petit blastomère postérieur P1. Cette asynchronie de division est sous le contrôle des protéines PAR qui sont impliquées dans l'établissement de l'axe antéro-postérieur de l'embryon. A ce jour, les mécanismes moléculaires gouvernant ce processus d'asynchronie ne sont que partiellement compris. Des études menées précédemment ont établit que le retard de division observé dans le petit blastomère postérieur P1 était dû, en partie, à l'activation préférentielle dans cette cellule de ATL-1/CHK-1, protéines contrôlant la réponse à des erreurs dans le processus de réplication de l'ADN. L'analyse des autres mécanismes responsables de la différence temporelle d'entrée en mitose des deux cellules a été entreprise au cours de cette thèse. Nous avons considéré la possibilité que l'asynchronie de division était du à l'entrée préférentielle en mitose du grand blastomère AB. Nous avons établi que la protéine kinase PLK-1 (polo-like kinase 1), impliquée dans la régulation positive de la mitose, était distribuée de manière asymétrique dans l'embryon deux cellules. PLK-1 est en effet enrichi dans le blastomère AB. Cette localisation asymétrique de PLK-1 est sous le contrôle des protéines PAR et semble établie via une rétention de PLK-1 dans la cellule AB. Par ailleurs, nous avons démontré que l'inactivation partielle de plk-7 par interférence à ARN (RNAi) conduit à un délai de l'entrée en mitose de la cellule P1 spécifiquement, indépendamment des protéines régulatrices ATL-1/CHK-1. En conclusion, nous proposons un modèle de régulation temporelle de l'entrée en mitose dans l'embryon deux cellules de C. elegans basé sur deux mécanismes complémentaires. Le premier implique l'activation préférentielle des protéines ATL-1/CHK-1, et conduit à un retard d'entrée en mitose spécifiquement dans la cellule P1. Le second est basé sur la localisation asymétrique de la protéine kinase PLK-1 dans la cellule AB et induit une entrée précoce en mitose de cette cellule. Par ailleurs, nous avons étudié un mutant appelé t2190 qui réduit la différence temporelle d'entrée en mitose entre les cellules AB et P1. Nous avons démontré que ce mutant correspondait à un nouvel allèle du Bene par-1. De plus, nous avons analysé le rôle de NMY-2, une protéine myosine qui agit comme moteur moléculaire sur les filaments d'active; dans la régulation de l'asynchronie de division des blastomères AB et P1, indépendamment de sa fonction dans l'établissement de l'axe antéro-postérieur. Par ailleurs, nous avons commencé l'étude du mécanisme moléculaire régulant la localisation asymétrique entre les cellules AB et P1 de la protéine phosphatase CDC25, qui est également un important régulateur de l'entrée en mitose. En conclusion, ce travail de thèse a permis une meilleure compréhension des mécanismes gouvernant la progression du cycle cellulaire dans l'embryon précoce de C. elegans. Etant donné que la plupart des protéines impliquées dans ces processus sont conservées chez d'autres organismes multicellulaires, il apparaît probable que les mécanismes moléculaires révélés dans cette étude soit aussi utilisés chez ceux-ci.

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Com o objetivo de estudar o efeito de doses de N, P e K na produção e na nutrição mineral de duas cultivares de cupuaçuzeiro (Theobroma grandiflorum), um experimento foi instalado em Argissolo Vermelho-Amarelo na região da Amazônia Central. O delineamento experimental utilizado foi o de blocos casualizados, em parcelas subdivididas, com três repetições. Os tratamentos estudados nas parcelas foram: N1P1K1; N1 P1 K0; N1 P0 K1; N0 P1K1; N1 P1 K2; N1 P2 K1 e N2 P1 K1; e, nas subparcelas, as duas cultivares de cupuaçu: com e sem sementes. As doses de 0; 1 e 2 de N, P e K foram, respectivamente, de 0; 60 e 120 kg ha-1 de N, na forma de uréia; 0; 100 e 200 kg ha-1 de P2O5, na forma de superfosfato triplo, e 0; 80 e 160 kg ha-1 de K2O, na forma de cloreto de potássio. O presente trabalho não possibilitou uma recomendação oficial de adubação para o cupuaçu, mas apresentou tendências das necessidades nutricionais da cultura. Considerando a produção média das três safras analisadas, não houve efeito da adubação nitrogenada na produção de frutos nas duas cultivares, assim como não houve da adubação com a dose mais elevada de fósforo. Contudo, os efeitos da aplicação de potássio apresentaram-se mais lineares e positivos, principalmente para a cultivar com sementes. Os menores valores de produção de frutos foram obtidos nos tratamentos com ausência de fósforo.

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O experimento foi conduzido em estufa telada na FCAV/Unesp Câmpus Jaboticabal-SP, durante o período de novembro de 2005 a janeiro de 2007. O estudo teve por objetivo avaliar componentes do desenvolvimento e do estado nutricional de mudas de laranjeira 'Valência', enxertada sobre citrumeleiro 'Swingle', cultivado em substrato, em função de doses de nitrogênio, fósforo e potássio. O delineamento experimental foi o inteiramente casualizado, em esquema fatorial 3³ + 1, sendo 3 fatores (nitrogênio, fósforo e potássio), 3 doses e uma testemunha (sem adubação), com 3 repetições. A unidade experimental foi constituída de uma muda de laranjeira por sacolas de 5 dm-3, contendo 2,5 kg de substrato casca de Pinus e vermiculita. Os tratamentos foram constituídos pela aplicação das seguintes doses de nutrientes em mg por dm³ de substrato: N1/2:459, N1:918 e N2:1836; P1/2:92, P1:184 e P2: 368; K1/2:438, K1:876 e K2:1752. Aos 424 dias após a semeadura, as plantas foram divididas em raízes e parte aérea para a determinação da massa da matéria seca, altura, área foliar, diâmetro do caule e conteúdo de nutrientes. As adubações com N, P e K proporcionaram maior crescimento e maior acúmulo de N, P e K na parte aérea e nas raízes das mudas de laranjeira, em substrato de casca de Pinus e vermiculita, em relação à testemunha. A dose de 459 mg dm-3 de N e as doses de P e K 184 e 876 mg dm-3, respectivamente, proporcionaram melhor crescimento da parte aérea das mudas; porém, na dose recomendada de N de 918 mg dm-3, ocorreu maior crescimento do sistema radicular.