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Low-cost broadband photodetectors (PDs) based on group-IV materials are highly demanded. Herein, a vertical all group-IV graphene-i-n (Gr-i-n) structure based on sputtering-grown undoped Ge0.92Sn0.08/Ge multiple quantum wells (MQWs) on n-Ge substrate was proposed to realize efficient visible/shortwave infrared (VIS/SWIR) dual-band photoresponse. Harnessing Gr-germanium tin (GeSn)/Ge MQWs van der Waals heterojunctions, an extended surface depletion region was established, facilitating separation and transportation of photogenerated carriers at VIS wavelengths. Consequently, remarkable VIS/SWIR dual-band response ranging from 400 to 2000â nm with a rapid response time of 23â µs was achieved. Compared to the PD without Gr, the external quantum efficiency at 420, 660, and 1520â nm was effectively enhanced by 10.2-, 5.2-, and 1.2-fold, reaching 40, 42, and 50%, respectively. This research paves the way for the advancement of all group-IV VIS/SWIR broadband PDs and presents what we believe to be a novel approach to the design of low-cost broadband PDs.
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Fruit ripening is a complex developmental process, which is modulated by both transcriptional and post-translational events. Control of fruit ripening is important in maintaining moderate quality traits and minimizing postharvest deterioration. In this study, we discovered that the transcription factor MaMYB4 acts as a negative regulator of fruit ripening in banana. The protein levels of MaMYB4 decreased gradually with banana fruit ripening, paralleling ethylene production, and decline in firmness. DNA affinity purification sequencing combined with RNA-sequencing analyses showed that MaMYB4 preferentially binds to the promoters of various ripening-associated genes including ethylene biosynthetic and cell wall modifying genes. Furthermore, ectopic expression of MaMYB4 in tomato delayed tomato fruit ripening, which was accompanied by downregulation of ethylene biosynthetic and cell wall modifying genes. Importantly, two RING finger E3 ligases MaBRG2/3, whose protein accumulation increased progressively with fruit ripening, were found to interact with and ubiquitinate MaMYB4, contributing to decreased accumulation of MaMYB4 during fruit ripening. Transient overexpression of MaMYB4 and MaBRG2/3 in banana fruit ripening delayed or promoted fruit ripening by inhibiting or stimulating ethylene biosynthesis, respectively. Taken together, we demonstrate that MaMYB4 negatively modulates banana fruit ripening, and that MaMYB4 abundance could be regulated by protein ubiquitination, thus providing insights into the role of MaMYB4 in controlling fruit ripening at both transcriptional and post-translational levels.
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Musa , Etilenos/metabolismo , Frutas/metabolismo , Regulación de la Expresión Génica de las Plantas , Musa/genética , Musa/metabolismo , Proteínas de Plantas/metabolismo , Ubiquitina-Proteína Ligasas/metabolismoRESUMEN
The process of extracting gold by biological oxidation involves oxidizing the refractory high-sulfur and high-arsenic ore with the help of bacteria to decompose the wrapping material of gold to extract the gold. Therefore, maximizing the activity of bacteria will directly affect the efficiency of gold extraction, for which it is particularly important to maintain the pulp temperature in the oxidation tank at the optimal bacteria breeding temperature. However, gold mines are generally located in mountainous areas, and the large temperature difference between day and night in winter, coupled with the influence of wind and snow, creates variations in the temperature in the oxidation tank. The traditional temperature measurement method cannot fully reflect the temperature change of the oxidation tank. As a multi-field application method, sensor information fusion can effectively address the problem of pulp temperature measurement. First, we analyzed the heat transfer principle inside the oxidation tank, and designed the cluster hierarchical sensor network according to the spatial position of each oxidation tank and the environmental interference factors. The network structure is divided into three layers; the bottom of the sensor to collect pulp temperature data shows a spiral distribution in the inner wall of the oxidation tank. Each cluster head node sensor is used as an intermediate layer to complete local measurement fusion estimation. Finally, the fusion center is taken as the upper layer to realize the global state fusion estimation. Secondly, in the data processing of the bottom temperature sensor, the traditional unscented Kalman filter (UKF) algorithm is improved and the fading memory matrix is added to improve the identification of nonlinear modeling errors. The sequential observation fusion estimator (SOFE) algorithm is embedded in the measurement update to improve the performance of local measurement fusion. Finally, in the global state fusion estimation, the sequential analysis is combined with the inverse covariance intersection, and the sequential analysis and inverse covariance intersection-global state fusion estimation (SICI-GSFE) algorithm is proposed. Through calculation and simulation, the results show that the external interference can be reduced by combining all the temperature state estimations, and the accuracy of the best global temperature state estimation is improved.
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Linoleic acid (LA; C18:2) and α-linolenic acid (ALA; C18:3) are two essential unsaturated fatty acids that play indispensable roles in maintaining membrane integrity in cold stress, and ω-3 fatty acid desaturases (FADs) are responsible for the transformation of LA into ALA. However, how this process is regulated at transcriptional and posttranscriptional levels remains largely unknown. In this study, an MYB transcription factor, MaMYB4, of a banana fruit was identified and found to target several ω-3 MaFADs, including MaFAD3-1, MaFAD3-3, MaFAD3-4 and MaFAD3-7, and repress their transcription. Intriguingly, the acetylation levels of histones H3 and H4 in the promoters of ω-3 MaFADs were elevated in response to cold stress, which was correlated with the enhancement in the transcription levels of ω-3 MaFADs and the ratio of ALA/LA. Moreover, a histone deacetylase MaHDA2 physically interacted with MaMYB4, thereby leading to the enhanced MaMYB4-mediated transcriptional repression of ω-3 MaFADs. Collectively, these data demonstrate that MaMYB4 might recruit MaHDA2 to repress the transcription of ω-3 MaFADs by affecting their acetylation levels, thus modulating fatty acid biosynthesis. Our findings provided new molecular insights into the regulatory mechanisms of fatty acid biosynthesis in cold stress in fruits.
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Ácido Graso Desaturasas/metabolismo , Frutas/metabolismo , Histona Desacetilasas/metabolismo , Musa/metabolismo , Proteínas de Plantas/metabolismo , Respuesta al Choque por Frío/genética , Respuesta al Choque por Frío/fisiología , Frutas/genética , Musa/genética , Proteínas de Plantas/genética , Factores de Transcripción/genética , Factores de Transcripción/metabolismoRESUMEN
With the aim of establishing a rapid method to discriminate Boletus tomentipes samples from different regions, FTIR spectroscopy with the aid of principal component analysis and clustering analysis were used in the present study. The information of infrared spectra of B. tomentipes samples originated from 15 regions has been collected. The original infrared spectra was pretreated by multiplicative signal correction (MSC) in combination with second derivative and Norris smooth. The spectral data were analyzed by principal component analysis and cluster analysis after the optimal pretreatment of MSC+SD+ND (15, 5), and the reasons for the differences of B. tomentipes samples from different regions could be explained through the principal component loading plot. The results showed that, the RSDs of repeatability, accuracy and stability of the method were 0.17%, 0.08% and 0.27%, respectively, which indicated the method was stable and reliable. The cumulative contribution of first three principal components of PCA was 87.24% which could reflect the most information of the samples. Principal component scores scatter plot displaying the samples from same origin could clustered together and samples from different areas distributed in a relatively independent space. Which can distinguish samples collected from different origins, effectively. The loading plot of principal component showed that with the principal component contribution rate decreasing, the captured sample information of principal component was also reducing. In the wave number of 3 571, 2 958, 1 625, 1 456, 1 405, 1 340, 1 191, 1 143, 1 084, 935, 840, 727 cm-1, the first principal component captured a large amount of sample information which attributed to carbohydrates, proteins, amino acids, fat, fiber and other chemical substances. Which showed that the different contents of these chemical substances may be the basis of discrimination of B. tomentipes samples from different origins. Cluster analysis based on ward method and Euclidean distance has shown the classification and correlation among samples. Samples originated from 15 regions could be clustered correctly in accordance with the basic origins and the correct rate was 93.33%. Which can be used to identify and analyze B. tomentipes collected from different sites. Fourier transform infrared spectroscopy combined with principal component analysis and cluster analysis can be effectively used to discriminate origins of B. tomentipes mushrooms and the reasons for the differences of B. tomentipes samples from different regions could be explained. This method could provide a reliable basis for discrimination and application of wild edible mushrooms.
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Fourier transform infrared spectroscopy combined with chemometrics was used to establish a method for rapid identification of different species of bolete mushrooms and determination of total mercury (Hg). In this study, 15 species of bolete mushrooms were used and the information of infrared spectra of 48 samples was collected. Meanwhile, the total Hg was determined with cold-vapour atomic absorption spectroscopy and direct mercury analyzer. The food safety of bolete mushrooms was evaluated according to provisional tolerable weekly intake (PTWI) for Hg recommended by the United Nations food and agriculture organization and the World Health Organization (FAO/WHO). The original infrared spectra were optimized with Norris smooth, multiplicative signal correction (MSC), second derivative, orthogonal signal correction and wavelet compression (OSCW). The spectra data were analyzed with principal component analysis (PCA) and partial least squares discriminant analysis (PLS-DA) after the optimal pretreatment. Then the discrimination model for different species of bolete mushrooms and prediction model of Hg content were established, respectively. The results showed that: (1) The cumulative contribution of first three principal components of PCA was 77.1%. Different species of boletes can be obviously distinguished in principal component score plot. It indicated that the chemical composition or contents were different in these species of boletes. (2) There were significant differences in total Hg contents in different samples and the total Hg content in the boletes were 0.17ï½15.2 mg·kg-1 dry weight (dw). If adults (60 kg) ate 300 g fresh bolete mushrooms a week, Hg intakes in a few samples were higher than the PTWI standard with potential risks. (3) The infrared spectra data in combination with the total Hg content was performed by partial least squares discriminant analysis. The mushroom samples with low (≤1.95 mg·kg-1 dw), medium (2.05ï½3.9 mg·kg-1 dw) and high (≥4.1 mg·kg-1 dw) total Hg content could be discriminated. Moreover, the more different the Hg content was, the more easily to distinguish. In addition, the prediction model of total Hg content of boletes was established. The R2 and RMSEE of the training set were 0.911 4 and 1.09, respectively while R2 and RMSEP of validation set were 0.949 7 and 0.669 5, respectively. The predictive values of total Hg content in boletes were approximate to the measured values which showed that the model has good predictive effect. Infrared spectroscopy combined with chemometrics can be used for rapid identification of bolete species and discrimination of bolete samples with different contents of total Hg. Furthermore, the total Hg content could also be predicted, accurately. This study may provide a rapid and simple method for quality control and edible safety assessment of wild-grown bolete mushrooms.
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Agaricales , Análisis de los Mínimos Cuadrados , Mercurio , Análisis de Componente Principal , Espectrofotometría Atómica , Espectroscopía Infrarroja por Transformada de FourierRESUMEN
In order to establish a rapid method for discriminating Boletus edulis mushroom, Fourier transform infrared spectroscopy combined with multivariate statistical analysis were used to study B. edulis which were collected from different origins and different years. The original infrared spectra of all the 152 B. edulis samples collected from 2011 to 2014 and 26 different areas of Yunnan Province were optimized with orthogonal signal correction and wavelet compression (OSCW) method. The spectral data that before and after being preprocessed with OSCW were analyzed with partial least squares discriminant analysis (PLS-DA). The classification results of PLS-DA were compared. Then the 152 B. edulis samples were randomly divided into a training set (120) and a validation set (32) to establish the PLS classification prediction model. The results showed that, after OSCW processing, the classification result of PLS-DA was significantly better than the other one which was not processed by OSCW. Principal component score plot can accurately distinguish B. edulis samples collected from different years and different origins. It indicated that OSCW can effectively eliminate the noise of spectra and reduce the unrelated interference information about the dependent variables to improve the accuracy and calculation speed of spectral analysis. Before OSCW preprocessed, the R2 and RMSEE of PLS model of the training set were 0.790 1 and 21.246 5 respectively while R2 and RMSEP of the model of validation set were 0.922 5 and 14.429 2. After OSCW pretreatment, R2 and RMSEE of the training set were 0.852 3 and 17.238 1 while R2 and RMSEP of validation set were 0.845 4 and 20.87. It suggested that OSCW could improve the predictive effect of the training set, but the over-fitting of OSCW-PLS may reduce the predictive ability of validation set. Therefore, it was unsuitable to establish a model with OSCW combined with PLS. In a conclusion, OSCW combined with PLS-DA can eliminate a large amount of spectrum interference information. This method could accurately distinguish B. edulis samples collected from different years and different origins. It could provide a reliable basis for the discrimination and classification of wild edible fungi.
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Agaricales/química , Espectroscopía Infrarroja por Transformada de Fourier , China , Análisis Discriminante , Análisis de los Mínimos CuadradosRESUMEN
BACKGROUND: Phlebopus portentosus and mealy bugs form a fungus-insect gall on the roots of host plants. The fungus and mealy bugs benefit mutually through the gall, which is the key link in the nutritional mechanism of P. portentosus. The cavity of the fungus-insect gall provides an ideal shelter for mealy bugs survival and reproduction, but how does P. portentosus benefit from this symbiotic relationship? METHODOLOGY AND RESULTS: Anatomical examination of fungus-insect galls revealed that one or more mealy bugs of different generations were living inside the galls. The mealy bug's mouthpart could penetrate through the mycelium layer of the inside of the gall and suck plant juice from the host plant root. Mealy bugs excreted honeydew inside or outside the galls. The results of both honeydew agar medium and quartz tests showed that the honeydew can attract and promote the mycelial growth of P. portentosus. A test of the relationship between the honeydew and the formation of the fungus-insect gall showed that honeydew promoted gall formation. CONCLUSIONS: All experimental results in this study show that the honeydew secreted by mealy bugs can attract and promote the mycelial growth of P. portentosus, forming a fungus-insect gall, because mealy bugs' honeydew is rich in amino acids and sugars.