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African swine fever (ASF) is a serious animal disease, and has spread to Africa, Europe and Asia, causing massive economic losses. African swine fever virus (ASFV) is transmitted from a reservoir host (warthog) to domestic pigs via a sylvatic cycle (transmission between warthogs and soft ticks) and a domestic cycle (transmission between domestic pigs) and survives by expressing a variety of genes related to virus-host interactions. We evaluated differences in codon usage patterns among ASFV genotypes and clades and explored the common and specific evolutionary and genetic characteristics of ASFV sequences. We analysed the evolutionary relationships, nucleotide compositions, codon usage patterns, selection pressures (mutational pressure and natural selection) and viral adaptation to host codon usage based on the coding sequences (CDS) of key functional genes of ASFV. AT bias was detected in the six genes analysed, irrespective of clade. The AT bias of genes (A224L, A179L, EP153R) encoding proteins involved in interaction with host cells after infection was high; among them, the AT bias of EP153R was the greatest at 78.3%. A large number of overrepresented codons were identified in EP153R, whereas there were no overrepresented codons with a relative synonymous codon usage (RSCU) value of ≥3 in B646L. In most genes, the pattern of selection pressure was similar for each clade, but in EP153R, diverse patterns of selection pressure were captured within the same clade and genotype. As a result of evaluating host adaptation based on the codon adaptation index (CAI), for B646L, E183L, CP204L and A179L, the codon usage patterns in all sequences were more similar to tick than domestic pig or wild boar. However, EP153R showed the lowest average CAI value of 0.52 when selecting tick as a reference set. The genes analysed in this study showed different magnitudes of selection pressure at the clade and genotype levels, which is likely to be related to the function of the encoded proteins and may determine key evolutionary traits of viruses, such as the level of genetic variation and host range. The diversity of codon adaptations at the genetic level in ASFV may account for differences in translational selection in ASFV hosts and provides insight into viral host adaptation and co-evolution.
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Vírus da Febre Suína Africana , Febre Suína Africana , Uso do Códon , Evolução Molecular , Seleção Genética , Vírus da Febre Suína Africana/genética , Vírus da Febre Suína Africana/classificação , Animais , Suínos , Febre Suína Africana/virologia , Febre Suína Africana/genética , Filogenia , GenótipoRESUMO
Unlike classical systems based on the use of morphological data, modern phylogenetic analyses use genetic information to construct phylogenetic trees. Ongoing research in the field of phylogenetics is evaluating the accuracy of phylogenetic estimation results and the reliability of phylogenetic trees to explain evolutionary relationships. Recently, the probability of stochastic errors in large-scale phylogenetic datasets has decreased, while the probability of systematic errors has increased. Therefore, before constructing a phylogenetic tree, it is necessary to assess the causes of systematic bias to improve the accuracy of phylogenetic estimates. We performed analyses of three datasets (Terebelliformia, Daphniid, and Glires clades) using bioinformatics software to assess systematic error and improve phylogenetic tree accuracy. Then, we proposed a combination of systematic biases capable of discerning the most suitable gene markers within a series of taxa and generating conflicting phylogenetic topologies. Our findings will help improve the reliability of phylogenetic software to estimate phylogenies more accurately by exploiting systematic bias.
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Filogenia , Software , Biologia Computacional/métodos , Animais , Reprodutibilidade dos TestesRESUMO
INTRODUCTION: Astrocytes are glial-type cells that protect neurons from toxic insults and support neuronal functions and metabolism in a healthy brain. Leveraging these physiological functions, transplantation of astrocytes or their derivatives has emerged as a potential therapeutic approach for neurodegenerative disorders. METHODS: To substantiate the clinical application of astrocyte-based therapy, we aimed to prepare human astrocytes with potent therapeutic capacities from human pluripotent stem cells (hPSCs). To that end, we used ventral midbrain patterning during the differentiation of hPSCs into astrocytes, based on the roles of midbrain-specific factors in potentiating glial neurotrophic/anti-inflammatory activity. To assess the therapeutic effects of human midbrain-type astrocytes, we transplanted them into mouse models of Parkinson's disease (PD) and Alzheimer's disease (AD). RESULTS: Through a comprehensive series of in-vitro and in-vivo experiments, we were able to establish that the midbrain-type astrocytes exhibited the abilities to effectively combat oxidative stress, counter excitotoxic glutamate, and manage pathological protein aggregates. Our strategy for preparing midbrain-type astrocytes yielded promising results, demonstrating the strong therapeutic potential of these cells in various neurotoxic contexts. Particularly noteworthy is their efficacy in PD and AD-specific proteopathic conditions, in which the midbrain-type astrocytes outperformed forebrain-type astrocytes derived by the same organoid-based method. CONCLUSION: The enhanced functions of the midbrain-type astrocytes extended to their ability to release signaling molecules that inhibited neuronal deterioration and senescence while steering microglial cells away from a pro-inflammatory state. This success was evident in both in-vitro studies using human cells and in-vivo experiments conducted in mouse models of PD and AD. In the end, our human midbrain-type astrocytes demonstrated remarkable effectiveness in alleviating neurodegeneration, neuroinflammation, and the pathologies associated with the accumulation of α-synuclein and Amyloid ß proteins.
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To investigate whether the defects in transient receptor potential canonical 4 (TRPC4), which is strongly expressed in the hippocampus, are implicated in ASD, we examined the social behaviors of mice in which Trpc4 was deleted (Trpc4-/-). Trpc4-/- mice displayed the core symptoms of ASD, namely, social disability and repetitive behaviors. In microarray analysis of the hippocampus, microRNA (miR)-138-2, the precursor of miR-138, was upregulated in Trpc4-/- mice. We also found that binding of Matrin3 (MATR3), a selective miR-138-2 binding nuclear protein, to miR-138-2 was prominently enhanced, resulting in the downregulation of miR-138 in Trpc4-/- mice. Some parameters of the social defects and repetitive behaviors in the Trpc4-/- mice were rescued by increased miR-138 levels following miR-138-2 infusion in the hippocampus. Together, these results suggest that Trpc4 regulates some signaling components that oppose the development of social behavioral deficits through miR-138 and provide a potential therapeutic strategy for ASD.
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Laminarin is a promising marine biopolymer that is abundant, non-toxic, and biodegradable. However, laminarin has a weak reduction potential for metal ions, resulting in the synthesis of a lower content of large-sized silver nanoparticles (AgNPs). Here, we showed that after the introduction of aldehyde groups, the reduction potential of laminarin increased, decreasing the synthesis time and increasing the density of AgNPs. 1H NMR and FT-IR confirmed the addition of aldehyde groups on laminarin. The dialdehyde-modified laminarin (DLAM) showed in situ, simple, and rapid synthesis of ultrasmall-sized spherical AgNPs (<10 nm), as revealed by TEM images. The aldehyde and carboxyl groups of DLAM act as synchronized reducing and anchoring agents. The conversion of Ag ions into AgNPs-DLAM was confirmed by UV-Vis spectrophotometer, FTIR, XRD, and XPS analysis. The AgNPs-DLAM showed significantly enhanced antibacterial activities than silver ions against Escherichia coli and Staphylococcus aureus via causing morphological changes and pore formations in bacterial cells. The AgNPs-DLAM also inhibited bacterial biofilm formation. In contrast, the AgNPs-DLAM showed negligible toxicity toward human keratinocytes. Furthermore, AgNPs-DLAM increased the migration of human keratinocytes, indicating efficient wound healing properties. Thus, signifying the importance of AgNPs-DLAM in clinical applications.
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Nanopartículas Metálicas , Prata , Humanos , Prata/farmacologia , Prata/química , Nanopartículas Metálicas/química , Testes de Sensibilidade Microbiana , Espectroscopia de Infravermelho com Transformada de Fourier , Antibacterianos/química , Cicatrização , Escherichia coli , AldeídosRESUMO
BACKGROUND: Primate lentiviruses (HIV1, HIV2, and Simian immunodeficiency virus [SIV]) cause immune deficiency, encephalitis, and infectious anemia in mammals such as cattle, cat, goat, sheep, horse, and puma. OBJECTIVE: This study was designed and conducted with the main purpose of confirming the overall codon usage pattern of primate lentiviruses and exploring the evolutionary and genetic characteristics commonly or specifically expressed in HIV1, HIV2, and SIV. METHODS: The gag, pol, and env gene sequences of HIV1, HIV2, and SIV were analyzed to determine their evolutionary relationships, nucleotide compositions, codon usage patterns, neutrality, selection pressure (influence of mutational pressure and natural selection), and viral adaptation to human codon usage. RESULTS: A strong 'A' bias was confirmed in all three structural genes, consistent with previous findings regarding HIV. Notably, the ENC-GC3s plot and neutral evolution analysis showed that all primate lentiviruses were more affected by selection pressure than by mutation caused by the GC composition of the gene, consistent with prior reports regarding HIV1. The overall codon usage bias of pol was highest among the structural genes, while the codon usage bias of env was lowest. The virus groups showing high codon bias in all three genes were HIV1 and SIVcolobus. The codon adaptation index (CAI) and similarity D(A, B) values indicated that although there was a high degree of similarity to human codon usage in all three structural genes of HIV, this similarity was not caused by translation pressure. In addition, compared with HIV1, the codon usage of HIV2 is more similar to the human codon usage, but the overall codon usage bias is lower. CONCLUSION: The origin viruses of HIV (SIVcpz_gor and SIVsmm) exhibit greater similarity to human codon usage in the gag gene, confirming their robust adaptability to human codon usage. Therefore, HIV1 and HIV2 may have evolved to avoid human codon usage by selection pressure in the gag gene after interspecies transmission from SIV hosts to humans. By overcoming safety and stability issues, information from codon usage analysis will be useful for attenuated HIV1 vaccine development. A recoded HIV1 variant can be used as a vaccine vector or in immunotherapy to induce specific innate immune responses. Further research regarding HIV1 dinucleotide usage and codon pair usage will facilitate new approaches to the treatment of AIDS.
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Infecções por HIV , Lentivirus de Primatas , Animais , Composição de Bases , Bovinos , Códon/genética , Infecções por HIV/genética , Cavalos/genética , Lentivirus de Primatas/genética , Mamíferos/genética , Seleção Genética , Ovinos/genéticaRESUMO
Autism or autism spectrum disorder (ASD) is a behavioral syndrome characterized by persistent deficits in social interaction, and repetitive patterns of behavior, interests, or activities. The gene encoding Methyl-CpG binding protein 2 (MeCP2) is one of a few exceptional genes of established causal effect in ASD. Although genetically engineered mice studies may shed light on how MeCP2 loss affects synaptic activity patterns across the whole brain, such studies are not considered practical in ASD patients due to the overall level of impairment, and are technically challenging in mice. For the first time, we show that hippocampal MeCP2 knockdown produces behavioral abnormalities associated with autism-like traits in rats, providing a new strategy to investigate the efficacy of therapeutics in ASD. Ketamine, an N-Methyl-D-aspartate (NMDA) blocker, has been proposed as a possible treatment for autism. Using the MeCP2 knockdown rats in conjunction with a rat model of valproic acid (VPA)-induced ASD, we examined gene expression and ASD behaviors upon ketamine treatment. We report that the core symptoms of autism in MeCP2 knockdown rats with social impairment recovered dramatically following a single treatment with ketamine. [BMB Reports 2022; 55(5): 238-243].
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Transtorno do Espectro Autista , Transtorno Autístico , Ketamina , Proteína 2 de Ligação a Metil-CpG , Animais , Transtorno do Espectro Autista/tratamento farmacológico , Transtorno do Espectro Autista/genética , Transtorno do Espectro Autista/metabolismo , Transtorno Autístico/tratamento farmacológico , Transtorno Autístico/genética , Transtorno Autístico/metabolismo , Modelos Animais de Doenças , Hipocampo/metabolismo , Ketamina/farmacologia , Proteína 2 de Ligação a Metil-CpG/deficiência , Proteína 2 de Ligação a Metil-CpG/genética , Proteína 2 de Ligação a Metil-CpG/metabolismo , Camundongos , RatosRESUMO
Depression is accompanied by neuronal atrophy and decreased neuroplasticity. Leucine-rich glioma-inactivated protein 1 (LGI1), a metastasis suppressor, plays an important role in the development of CNS synapses. We found that LGI1 expression was reduced in the hippocampi of mice that underwent chronic unpredictable stress (CUS), and could be rescued by the antidepressant, fluoxetine. Recombinant soluble neuritin, an endogenous protein previously implicated in antidepressant-like behaviors, elevated hippocampal LGI1 expression in a manner dependent on histone deacetylase 5 (HDAC5) phosphorylation. Accordingly, Nrn1 flox/flox ;Pomc-cre (Nrn1 cOE) mice, which conditionally overexpress neuritin, displayed increases in hippocampal LGI1 level under CUS and exhibited resilience to CUS that were blocked by hippocampal depletion of LGI1. Interestingly, neuritin-mediated LGI1 expression was inhibited by HNMPA-(AM)3, an insulin receptor inhibitor, as was neuritin-mediated HDAC5 phosphorylation. We thus establish hippocampal LGI1 as an effector of neurite outgrowth and stress resilience, and suggest that HDAC5-LGI1 plays a critical role in ameliorating pathological depression.
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In this study, microstructure and sintering behaviors of the gas-atomized Al-(25 or 30) Cr-xSi alloy (x = 5, 10 and 20 at.%) during spark plasma sintering (SPS) process were investigated. Gas-atomized alloy powders were manufactured using Ar gas atomizer process. These alloy powders were consolidated using SPS process at different temperature under pressure 60 MPa in vacuum. Microstructures of the gas-atomized powders and sintered alloys were analyzed using scanning electron microscopy (SEM) with energy-dispersive X-ray spectrometer (EDS), and transmission electron microscopy (TEM). Hardness of the SPS sintered alloys was measured using micro Vickers hardness tester. The Al-Cr-Si bulks with high Cr and Si content were produced successfully using SPS sintering process without crack and obtained fully dense specimens close to nearly 100% T. D. (Theoretical Density). The maximum values of the hardness were 834 Hv for the sintered specimen of the gas atomized Al-30Cr-20Si alloy. Enhancement of hardness value was resulted from the formation of the multi-intermetallic compound with the hard and thermally stable phases and fine microstructure by the addition of high Cr and Si.
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In this study, changes in the microstructure, mechanical properties, and electrical conductivity of cast and extruded Al-Zn-Cu-Mg based alloys with the addition of Li (0, 0.5 and 1.0 wt.%) were investigated. The Al-Zn-Cu-Mg-xLi alloys were cast and homogenized at 570 °C for 4 hours. The billets were hot extruded into rod that were 12 mm in diameter with a reduction ratio of 38:1 at 550 °C. As the amount of Li added increased from 0 to 1.0 wt.%, the average grain size of the extruded Al alloy increased from 259.2 to 383.0 µm, and the high-angle grain boundaries (HGBs) fraction decreased from 64.0 to 52.1%. As the Li content increased from 0 to 1.0 wt.%, the elongation was not significantly different from 27.8 to 27.4% and the ultimate tensile strength (UTS) was improved from 146.7 to 160.6 MPa. As Li was added, spherical particles bonded to each other, forming an irregular particles. It is thought that these irregular particles contribute to the strength improvement.
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BACKGROUND: The large tumor antigen (LT-Ag) and major capsid protein VP1 are known to play important roles in determining the host-specific infection properties of polyomaviruses (PyVs). OBJECTIVE: The objective of this study was to investigate the physicochemical properties of amino acids of LT-Ag and VP1 that have important effects on host specificity, as well as classification techniques used to predict PyV hosts. METHODS: We collected and used reference sequences of 86 viral species for analysis. Based on the clustering pattern of the reconstructed phylogenetic tree, the dataset was divided into three groups: mammalian, avian, and fish. We then used random forest (RF), naïve Bayes (NB), and k-nearest neighbors (kNN) algorithms for host classification. RESULTS: Among the three algorithms, classification accuracy using kNN was highest in both LT-Ag (ACC = 98.83) and VP1 (ACC = 96.51). The amino acid physicochemical property most strongly correlated with host classification was charge, followed by solvent accessibility, polarity, and hydrophobicity in LT-Ag. However, in VP1, amino acid composition showed the highest correlation with host classification, followed by charge, normalized van der Waals volume, and solvent accessibility. CONCLUSIONS: The results of the present study suggest the possibility of determining or predicting the host range and infection properties of PyVs at the molecular level by identifying the host species of active and emerging PyVs that exhibit different infection properties among diverse host species. Structural and biochemical differences of LT-Ag and VP1 proteins in host species that reflect these amino acid properties can be considered primary factors that determine the host specificity of PyV.
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Antígenos Transformantes de Poliomavirus/química , Proteínas do Capsídeo/química , Aprendizado de Máquina , Polyomavirus/classificação , Aminoácidos/química , Especificidade de Hospedeiro , FilogeniaRESUMO
Astrocytes and microglia are brain-resident glia that can establish harmful inflammatory environments in disease contexts and thereby contribute to the progression of neuronal loss in neurodegenerative disorders. Correcting the diseased properties of glia is therefore an appealing strategy for treating brain diseases. Previous studies have shown that serum/ glucocorticoid related kinase 1 (SGK1) is upregulated in the brains of patients with various neurodegenerative disorders, suggesting its involvement in the pathogenesis of those diseases. In this study, we show that inhibiting glial SGK1 corrects the pro-inflammatory properties of glia by suppressing the intracellular NFκB-, NLRP3-inflammasome-, and CGAS-STING-mediated inflammatory pathways. Furthermore, SGK1 inhibition potentiated glial activity to scavenge glutamate toxicity and prevented glial cell senescence and mitochondrial damage, which have recently been reported as critical pathologic features of and therapeutic targets in Parkinson disease (PD) and Alzheimer disease (AD). Along with those anti-inflammatory/neurotrophic functions, silencing and pharmacological inhibition of SGK1 protected midbrain dopamine neurons from degeneration and cured pathologic synuclein alpha (SNCA) aggregation and PD-associated behavioral deficits in multiple in vitro and in vivo PD models. Collectively, these findings suggest that SGK1 inhibition could be a useful strategy for treating PD and other neurodegenerative disorders that share the common pathology of glia-mediated neuroinflammation.
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Glucocorticoides , Doença de Parkinson , Animais , Modelos Animais de Doenças , Neurônios Dopaminérgicos , Humanos , Modelos Animais , Neuroglia , Doença de Parkinson/tratamento farmacológicoRESUMO
The effect of addition of Mischmetal (MM) on the microstructure, electrical and thermal conductivity, and mechanical properties of the as-extruded Al-MM based alloys were investigated. The studied AlxMM alloys (where x = 0.2, 0.5, 1.0, 1.5, 2.0 and 5.0 wt.%) were cast and homogenized at 550 °C for 4 h. The cast billets were extruded into 12 mm bars with an extrusion ratio of 39 at 550 °C. The addition of MM resulted in the formation of Al11(Ce, La)3 intermetallic compounds and the area fraction of these intermetallic compounds increased with an increase in the MM content. The Al11(Ce, La)3 phase, which was distributed in the as-cast alloys, was crushed into fine particles and arrayed along the extruded direction during the extrusion process. In particular, these intermetallic compounds in the extruded Al-5.0MM alloy were distributed with a wide-band structure due to the fragmentation of the eutectic phase with a lamellar structure. As the MM content increased from 1.0 wt.% to 5.0 wt.%, the average grain size decreased remarkably from 740 to 73 µm. This was due to formation of Al11(Ce, La)3 particles during the hot extrusion process, which promoted dynamic recrystallization and suppression of grain growth. The electrical and thermal conductivity of the extruded alloys containing up to 2.0 wt.% MM were around 60.5% IACS and 230 W/m · K, respectively. However, the electrical and thermal conductivity of the extruded alloy with 5.0 wt.% MM decreased to 55.4% IACS and 206 W/m · K, respectively. As the MM content increased from 1.0 wt.% to 5.0 wt.%, the ultimate tensile strength (UTS) was improved remarkably from 74 to 119 MPa which was attributed to the grain refinement and formation of Al11(Ce, La)3 intermetallic compounds by the addition of MM.
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The workability of Al-xMg alloys with a high Mg content (Al-6Mg, Al-8Mg, Al-9Mg) was evaluated by investigating the microstructure and processing map. Hot torsion tests were conducted in the range of 350-500 °C between 0.1 and 1 s-1. Constitutive equations were derived from various effective stress-strain curves, and the thermal activation energies for deformation obtained were 171 kJ/mol at Al-6Mg, 195 kJ/mol at Al-8Mg, and 220 kJ/mol at Al-9Mg. In the case of the processing map, the instability region, which widened with increasing Mg content, was due mainly to the influence of the Mg solute, which activated grain boundary cracking and flow localization.
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Microstructure and properties of Al-2 wt.%Zn-1 wt.%Cu-xMg (x = 0.1, 0.3, 0.5, 0.7 wt.%) alloy extrusion materials were investigated. The lattice constants for the (311) plane increased to 4.046858, 4.048483, 4.050114 and 4.051149 Å with the addition of 0.1, 0.3, 0.5, and 0.7 wt.% of elemental Mg. The average grain size of the as-extruded Al alloys was found to be 328.7, 297.7, 187.0 and 159.3 µm for the alloys with 0.1, 0.3, 0.5, and 0.7 wt.% Mg content, respectively. The changes in the electrical conductivity by the addition of elemental Mg in Al-2 wt.%Zn-1 wt.%Cu alloy was determined, and it was found that for the addition of 0.1, 0.3, 0.5, and 0.7 wt.% Mg, the conductivity decreased to 51.62, 49.74, 48.26 and 46.80 %IACS. The ultimate tensile strength of Al-2 wt.%Zn-1 wt.%Cu-0.7 wt.%Mg alloy extrusion was increased to 203.55 MPa. Thus, this study demonstrated the correlation between the electrical conductivity and strength for the Al-2 wt.%Zn-1 wt.%Cu-xMg alloys.
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Commercial vehicle pistons should have low thermal expansion and should be able to withstand deformation or mechanical stress. Aluminum alloys are suitable for pistons due to their light weight. However, as aluminum alloys have low strength and friction resistance, cast iron is added through the dipping process in order to increase the quality of pistons. However, the dipping process leads to defects such as defective bonding, void formation, and formation of an oxidation film at the junctions of the two materials due to differences in their properties, which adversely affects the impact resistance and mechanical strength of the product. A theoretical study on the metallurgical bond between the aluminum alloy and the cast iron insert in the piston was conducted to investigate the cause of the defects. The microstructure of the intermetallic bonding layer was observed using scanning electron microscopy and electron dispersive spectroscopy. In this study, defects were found in non-bonding and oxide films and several phases were generated corresponding to different parameters. It was found that processing time and temperature were the main causes of these defects.
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Rift Valley fever virus (RVFV) is a vector-borne pathogen and is the most widely known virus in the genus Phlebovirus. Since it was first reported, RVFV has spread to western Africa, Egypt and Madagascar from its traditional endemic region, and infections continue to occur in new areas. In this study, we analyzed genomic patterns according to the infection properties of RVFV. Among the four segments of RVFV, the nucleotide composition, overall GC content and the difference of GC composition in the third position of the codons (%GC3) between groups were the largest in the S (NP) segment, showing that more diverse codons were used than in other segments. Furthermore, the results of CAI analysis of the S (NP) segment showed that viruses isolated from regions where no previous infections had been reported had the highest values, indicating greater adaptability to human hosts compared with other viruses. This result suggests that mutations in the S (NP) segment co-evolve with the infected hosts and may lead to expansion of the geographic range. The distinctive codon usage patterns observed in specific genomic regions of a group with similar infection properties may be related to the increasing likelihood of RVFV infections in new areas.
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Thermal properties and microstructure of Al-4 wt.% Zn-2 wt.% Cu-x (x = 2 wt%. Mg, 2 wt%. Sn, 0.7 wt.% Mg-0.7 wt.% Sn-0.7 wt.% Ca) alloys on cast and extrusion have been investigated with extrusion temperature of 400 °C. Al-4 wt.% Zn-2 wt.% Cu alloy was composed of Al and Al2Cu phases. By adding Mg contents, Al2Mg3Zn3 phase was increased and Al2Cu phase was decreased respectively. During hot extrusion, elongated in the extrusion direction because of severe deformation. The thermal conductivity with temperature and composition of as-extruded Al-4 wt.% Zn-2 wt.% Cu-x alloys decreases with adding 2 wt.% Mg, 2 wt.% Sn contents from 190.925 and 196.451 W/mK but thermal properties of addition of 0.7 wt.% Mg-0.7 wt.% Sn-0.7 wt.% Ca element slightly reduced from 222.32 to 180.775 W/mK. The ultimate tensile strength (UTS) for Al-4 wt.% Zn- 2 wt.% Cu alloy was 121.67 MPa. By adding 2 wt.% Mg contents, tensile strength was dramatically increased with 350.5 MPa.
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In this research, effects of Zn and Cu content on microstructure, mechanical properties, electric and thermal conductivity of the as-extruded Al-x(Zn+0.5Cu) alloys were investigated. As the content of Zn and Cu increased, the area ratio of Al2Cu intermetallic compounds increased. After homogenization treatment and extrusion process, most of Al2Cu intermetallic compounds was disappeared due to solution in Al matrix of Cu atoms. As the (Zn+0.5Cu) content increased from 1 to 2 wt.%, the average grain size decreased remarkably from 645 to 227 µm due to the dynamic recrystallization caused by the solute Zn and Cu atoms during the extrusion. With increasing Zn and Cu additions, the thermal conductivity was decreased from 225 (x = 1) to 208 (x = 2) and 183 W/mK (x = 4) due to electric scattering by solute Zn and Cu atoms. The ultimate tensile strength (UTS) of the as-extruded Al-x(1Zn+0.5Cu) alloys improved remarkably from 77 (x = 1) to 142 MPa (x = 4) as Zn and Cu content increased, and the elongation increased from 30 to 33%. This improvement in the strength resulted from the grain refinement and solid solution strengthening due to the solute Zn and Cu atoms. The Zn and Cu addition in Al alloy played an important role in thermal conductivity and mechanical properties.
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High conductivity Al alloys are widely used for electric materials, heat exchangers, and heat dissipation parts such as electric conductors, transmission lines, communication cables, automobile wires and so on. In this study, the effects of Ca and Mn addition on the microstructure and mechanical properties of Al-0.3Cu-0.2Fe-0.15Si-0.15Zn alloys were investigated. The melt was held at 800 °C for 20 minutes and poured into a mold. The cast Al alloy was hot extruded with a rod having a diameter of 12 mm and a reduction ratio of 38:1. Al-0.3Cu-0.2Fe-0.15Si-0.15Zn-0.9Mn-0.4Ca alloy consists of Al, Al-(Fe, Mn)-Si, Al-(Fe, Mn) and Al-(Ca) intermetallic compounds. The formation of the intermetallic compound and this phase was broken in to small particles during extrusion. As the Ca content increased from 0 to 0.4 wt.%, the electrical conductivity of the extruded Al-0.3Cu- 0.2Fe-0.15Si-0.15Zn alloys increased by 57.3, 57.9 and 59.0 %IACS (International annealed copper standard). Al-0.3Cu-0.2Fe-0.15Si-0.15Zn-0.9Mn alloy with element additions of Ca, ultimate tensile strength was decreased from 178.3 to 163.2 and 151.8 MPa. However, the elongation was improved to 18.6, 21.6 and 23.15%.