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    Crop Science
    Effect of change of plant height on nitrogen use efficiency in Yongyou indica-japonica hybrid rice
    WANG Feng, SHEN Jianghua, SUN Meimei, CHAI Weigang, YAO Hongyan, DAI Yaolu, ZHANG Yuping, ZHU Defeng, CHEN Ruoxia
    2019, 31(1):  1-10.  DOI: 10.3969/j.issn.1004-1524.2019.01.01
    Abstract ( 528 )   HTML ( 88 )   PDF (1188KB) ( 1678 )  
    A field experiment was conducted to determine the precise effects of plant height on the grain yield and nitrogen use efficiency (NUE) in Yongyou indica-japonica hybrid rice, which aimed to provide reference data for rice breeding and high-NUE management of Yongyou series. This study was carried out at the single-season rice area of the coastal region of East Zhejiang (Sizhoutou town, Xiangshan County) in 2016. Six rice cultivars different in plant height (high straw, Yongyou12 & Yongyou15; medium straw, Yongyou7850 & Yongyou2640; short straw, Yongyou538 & Yongyou1540) and two treatments of chemical N application rates (N0, 0 kg·hm-2; N270, 270 kg·hm-2) were chosen for this study. Our results showed that the grain yield followed the sequence of Yongyou7850>Yongyou2640>Yongyou538>Yongyou1540>Yongyou12>Yongyou15 in different N treatments. Significant positive correlation was observed between grain yield and the maximum tiller number and effective panicle. Chemical N fertilization resulted in an increase of plant height, maximum tiller number and effective panicle. N recovery efficiency (NRE), N agronomy efficiency (NAE) and N partial factor productivity (NPFP) showed inconsistent trends in different cultivars. The NER in Yongyou12 and Yongyou15 were 37.4% and 36.4%, respectively, which were significantly higher than other cultivars (<30%). Contrarily, NPFP was significantly lower than Yongyou7850, Yongyou2640 and Yongyou538. Importantly, N harvest index (NHI) was the lowest in Yongyou12, indicating rice plant in the luxurious absorption of nitrogen. N surpluses were found in all rice cultivars under N treatments. N surpluses in Yongyou1540, Yongyou538, Yongyou15 and Yongyou7850 was more than 60 kg·hm-2, which was significantly higher than Yongyou2640 and Yongyou12. In conclusion, under the conventional practice conditions in the coastal region of East Zhejiang, the NUE of Yongyou series rice in high straw was higher than medium or short straw, while the grain yield was contrast because of biomass production and straw luxurious absorption of nitrogen.
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    Cloning and expression analysis of oxalate oxidase gene MsOXO from Medicago sativa
    XU Qingsong, ZHAO Jia, WEI Yunmin, HAN Rongrong, LIU Lusheng, JIANG Caode, YU Yong-xiong
    2019, 31(1):  11-19.  DOI: 10.3969/j.issn.1004-1524.2019.01.02
    Abstract ( 652 )   HTML ( 1 )   PDF (1612KB) ( 1662 )  
    Oxalate oxidase plays an important role in defence of various pathogens such as Sclerotinia and can be used for plant improvement. To explore the role of oxalate oxidase in the defense of Sclerotinia sclerotiorum, alfalfa was used for material in this study, an oxalate oxidase gene, MsOXO, was successfully cloned. Subcellular localization of MsOXO was performed using the transient expression of tobacco, and the result showed that MsOXO was located in cell wall. The results of qRT-PCR showed that MsOXO was expressed in roots, stems and leaves of alfalfa, but was lower in roots and stems, which might be the reason why the root neck and stem base were more susceptible to infection by the pathogen. The up-regulated expression of MsOXO gene was induced by exogenous oxalic acid 50 μmol·L-1 treated root or 100 μmol·L-1 treated stem and exogenous salicylic acid 100 μmol·L-1 treated root.
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    OAnimal Science
    Establishment of a multiplex PCR assay for three pathogenic bacteria in cows with recessive mastitis
    WANG Yu, LI Bi, YANG Mingxian, ZUO Zhicai
    2019, 31(1):  20-29.  DOI: 10.3969/j.issn.1004-1524.2019.01.03
    Abstract ( 824 )   HTML ( 1 )   PDF (1911KB) ( 1699 )  
    In order to establish a method for the rapid and simultaneous detection of three pathogenic bacteria of mastitis of Streptococcus agalactiae, Staphylococcus aureus and Pseudomonas aeruginosa, three pairs of specific primers were synthesized based on the Streptococcus agalactiae 16S rRNA gene, Staphylococcus aureus NUC heat-resistance gene, Pseudomonas aeruginosa ETA gene sequence and references. By adjusting and optimizing the parameters of the PCR reaction, a multiplex PCR detection system was established, and the sensitivity test and specificity test were simultaneously performed. The results showed that the detection method can simultaneously amplify specific fragments of 270 bp of Streptococcus agalactiae, 153 bp of Staphylococcus aureus and 375 bp of Pseudomonas aeruginosa and a generic 1 500 bp fragment of bacterial 16S rRNA. For other six kinds of pathogenic bacteria, only 1 500 bp universal fragments could be amplified, which had strong specificity. Three specific primer amplification bands were 99% homologous to the GenBank and bacterial gene sequences. After culture for 24 h, the minimum sensitivity of the system to Streptococcus agalactiae, Staphylococcus aureus and Pseudomonas aeruginosa was 8×104, 4×104 and 1.5×105 CFU·mL-1, respectively. The detection method established in this study can complete the rapid detection of Streptococcus agalactiae, Staphylococcus aureus and Pseudomonas aeruginosa, and is of great significance for the differential diagnosis and rapid detection of subclinical mastitis in dairy cows.
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    Prokaryotic expression and bioinformatics analysis of orf virus Anhui strain 023 gene
    ZHANG Gaofeng, YANG Kankan, ZHANG Qian, WANG Yuanhong, YU Zhaorong, ZHANG Xueqi, LU Zhimin, LIU Zimin, LI Yongdong, WANG Yong
    2019, 31(1):  30-38.  DOI: 10.3969/j.issn.1004-1524.2019.01.04
    Abstract ( 531 )   HTML ( 0 )   PDF (1585KB) ( 1544 )  
    Our study was aimed at cloning and expressing the 023 gene of orf virus (ORFV) Anhui strain, and predicting its biological characteristics. The 023 gene was amplified by PCR, then successfully expressed using a prokaryotic vector. Then, the expressed protein was purified, and identified by SDS-PAGE and Western-blot. In addition, the physicochemical properties, secondary structure, signal peptide, transmembrane domain of the protein was analyzed by bioinformatics software. The results showed that the 023 gene of ORFV Anhui strain was 819 bp in length which could encode 272 amino acids. The size of expressed protein was approximately 42 ku, which was mainly expressed in inclusion body form with good reactogenicity. The results from bioinformatics analysis showed that the protein was a hydrophilic stable protein. There were 27.57% α-helix (h), 17.28% extended chain (e), 12.13% β-turn (t), 43.01% random coli (c). There was no signal peptide region and transmembrane domain. Maybe, it had 30 phosphorylation sites. Moreover, there were four B cell epitopes, three CTL epitopes and three Th epitopes. In conclusion, our study could provide a reference for further study of the structure and function of ORFV 023 gene.
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    Effect and correlation analysis of Eimeria tenella infection on IL-6, IL-8 and CCLi2 genes expression in spleen and caecum of Jinghai Yellow Chicken (Gallus gallus)
    XIN Shijie, WANG Xiaohui, DAI Guojun, AN Tingting, ZHANG Tao, ZHANG Genxi, XIE Kaizhou, WANG Jinyu, WANG Hongsheng
    2019, 31(1):  39-46.  DOI: 10.3969/j.issn.1004-1524.2019.01.05
    Abstract ( 529 )   HTML ( 0 )   PDF (1105KB) ( 1654 )  
    Interleukin 6 (IL-6), interleukin 8 (IL-8) and CC motif chemokine ligand 2 (CCLi2) play an important role in the inflammatory response and immune. In this study, in order to reveal the expression relationships between the three genes in spleen, caecum and between spleen and caecum at coccidiosis infected and non-infected state, Jinghai Yellow Chicken(Gallus gallus) were divided into coccidiosis infection and non-infection group, the relative expression of mRNA of IL-6, IL-8 and CCLi2 in spleen and caecum was detected by quantitative real-time polymerase chain reaction (qRT-PCR), the relative expression difference of the three genes were compared between infection and control group in the same tissue, meanwhile, the relative expression correlation were analyzed among the three genes in the same and different tissues within the same group. The results showed that the relative expression levels of IL-6, IL-8 and CCLi2 genes in spleen tissue of infected group were all higher than those of the control group (P<0.05), and the relative expression level of IL-6 gene in infected group was extremely significant different from control group (P<0.01); the relative expression levels of IL-6, IL-8 and CCLi2 genes in the caecum tissue of infected group were all extremely significant different from that of the control group (P<0.01). The correlation analysis showed that the correlation coefficient between the expression of IL-6, IL-8 and CCLi2 genes in spleen tissues of infected group were all positively related (P<0.01); in caecum tissue of infected group, there were extremely significant positive correlations(P<0.01) among the relative expression of the IL-8, CCLi2 with IL-6 genes, but the relative expression correlation between IL-8 and CCLi2 genes was not significant correlated (P>0.05); in the spleen tissue of the control group, there were extremely significant positive correlations (P<0.01) between the relative expression of IL-6, IL-8 with CCLi2 genes, and the correlation between other genes in the control group was not significant (P>0.05); there were extremely significant positive correlations (P<0.01) among the three genes of IL-6, IL-8 and CCLi2 in the caecum tissue of the control group; the correlation analysis results also showed that the expression of the three genes was not significantly correlated (P>0.05) between spleen and caecum tissue, regardless of the infection group or the control group. All of the results indicated that IL-6, IL-8 and CCLi2 might play an important role in the process of Jinghai Yellow Chicken coccidiosis infection, and the results provided the basis for further exploring the role of these three genes in the genetic breeding of coccidiosis resistance, and it had an important significance for Jinghai Yellow Chicken genetic breeding of coccidiosis resistance.
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    Study on microbial community structure in chilled chicken during cold storage
    GUI Guohong, YANG Hua, ZHU Jiangqun, ZHU Jianfeng, XIAO Yingping, XU E
    2019, 31(1):  47-55.  DOI: 10.3969/j.issn.1004-1524.2019.01.06
    Abstract ( 498 )   HTML ( 0 )   PDF (1191KB) ( 1611 )  
    To explore the changes of microbial community structure in chilled chicken during cold storage, 25 chilled chicken samples were obtained from poultry slaughterhouse in east China and stored in 4 ℃. Five chilled chickens were used to measure the concentration of total volatile basic nitrogen (TVBN), total number of bacterial colonies and total E.coli counts on day 0, 1, 3, 5, 7, respectively. The bacterial community structures were analyzed by high-throughput sequencing. Results showed that the concentration of TVBN enhanced with the increasing cold storage days, from 5.51 mg·(100 g)-1 to 29.84 mg·(100 g)-1 (P<0.05). The total number of bacterial colonies were also increased, from 4.46 × 106 CFU·g-1 to 1.87 ×108 CFU·g-1 (P<0.05), while the total E.coli counts increased, from 1.48 × 106 CFU·g-1g to 5.18 × 106 CFU·g-1 (P<0.05). High-throughput sequencing showed that Proteobacteria, Firmicutes, Actinobacteria and Bacteroidetes were the dominant phyla, the relative abundance of these four phyla were more than 99% in chilled chickens of different storage days. At genus level, Lactobacillus, Acinetobacter, Psychrobacter, Enterococcus, Pseudomonas, and Escherichia were dominant. The genera with relative abundance more than 0.1% were selected for significance analysis among chilled chickens of different storage time. There were 9 genera of increased relative abundance, including Carnobacterium, Lactococcus, Macrococcus, Pseudomonas, Psychrobacter, and Shewanella, which were typical spoilage bacteria. Otherwise, 10 genera were of reduced relative abundance, including Bacteroides, Blautia, Enterococcus, Faecalibacterium, Ruminococcus, and SMB53, which were typical intestinal bacteria in broilers. These findings suggested that the contaminant microorganisms in chilled chicken were from broilers in the startup phase, and then the spoilage bacteria became the dominant microorganisms, which could result in the spoilage of chicken meat.
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    Adjuvant effect of E515-A on porcine epidemic diarrhea virus inactivated vaccine
    MA Yongqi, XU Wei, WANG Yuemin, HU Songhua
    2019, 31(1):  56-61.  DOI: 10.3969/j.issn.1004-1524.2019.01.07
    Abstract ( 575 )   HTML ( 0 )   PDF (1087KB) ( 1387 )  
    E515-A was a white oil containing ginseng stem and leaf saponins (GSLS). An oil emulsion vaccine was obtained by mixing E515-A and water phase containing porcine epidemic diarrhea virus (PEDV) antigen at a low shear force (200 r·min-1). To observe the adjuvant effect of E515-A on inactivated PEDV vaccine, 72 ICR mice were randomly divided into 6 groups and subcutaneously immunized twice at a two-weeks interval with the following solution, respectively: (1) physiological saline solution, (2) PEDV antigen+physiological saline solution, (3) PEDV antigen+GSLS, (4) PEDV antigen+white oil adjuvant, (5) PEDV antigen+E515-A, (6) PEDV antigen+aluminum hydroxide (alum). Serum IFN-γ and NK cytotoxicity were determined 24 h after primary immunization; serum specific IgG, IgG1 and IgG2a and splenic lymphocyte proliferation were analyzed after booster immunization. The results indicated that E515-A significantly enhanced the immune response to PEDV vaccine when compared with aluminum adjuvant. E515-A significantly promoted the killing activity of NK cells in immunized mice, increased the production of IFN-γ, enhanced the splenic lymphocytes proliferation to Concanavalin (Con A) and lipopolysaccharide (LPS) stimulation, and improved the level of serum IgG and its subclass IgG1 and IgG2a in comparison with the control group. To improve the immunity of pigs, E515-A as an adjuvant deserves further study for its use in swine vaccine.
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    Correlation analysis of growth traits and two microsatellite polymorphisms in flanking region of growth hormone gene in topmouth culter (Culter alburnus Basilewsky)
    LIU Shili, JIANG Wenping, CHENG Shun, CHI Meili, ZHENG Jianbo, JIA Yongyi, ZHAO Jinliang, GU Zhimin
    2019, 31(1):  62-68.  DOI: 10.3969/j.issn.1004-1524.2019.01.08
    Abstract ( 411 )   HTML ( 0 )   PDF (1035KB) ( 1391 )  
    The body length and weight of 120 topmouth culter (Culter alburnus Basilewsky) cultured in the same pond were measured. The polymorphism information and correlation with growth traits of two microsatellite loci, Cal-GH01 and Cal-GH02, located in the flanking regions of the growth hormone (GH) gene were analyzed. The results showed that three Cal-GH01 alleles (404, 407 and 410 bp) and six genotypes could be detected. The 407 bp allele was the dominant allele, and 407/407 bp was the dominant genotype. The polymorphic information content of the microsatellite locus was 0.420, and the heterozygosity was 0.207 2. A total of six alleles (366, 375, 378, 381, 384 and 387 bp) and 11 genotypes were detected for Cal-GH02. The 381 bp allele was the dominant allele, and 381/381 bp was the dominant genotype. The polymorphic information content of the microsatellite locus was 0.450, and the heterozygosity was 0.466 1, which made it a moderately polymorphic locus. The associations between the polymorphisms of the two loci and growth traits were analyzed using general linear models. The analysis results for microsatellite locus Cal-GH01 showed that 404/407-type individuals accounted for 13.3% of the sample size and had the longest body length. The 407/410-type individuals accounted for 5% of the sample weight and were the heaviest. There were some differences in body length and body weight among the Cal-GH01 genotypes; however, the differences were not significant (P>0.05). For microsatellite locus Cal-GH02, 366/381-type individuals accounted for 3.3% of the number of samples, and their body length and body weight were the highest. Their weight was significantly higher than that of the other genotypes (P<0.05). 384/387-type individuals accounted for 2.5% of the sample size, and their body length and weight were the lowest. Their body length was significantly lower than that of other genotypes (P<0.05). In conclusion, we studied the genetic characteristics of two microsatellite loci in 120 fish sampled from the same pond. The correlation analysis for body length and body weight provided a scientific basis for marker-assisted selection for growth traits. Overall, there were associations between polymorphisms in the GH gene and the growth traits of C. alburnus. Therefore, the two microsatellite loci in GH gene could be used as markers for practical breeding programs for growth traits in C. alburnus.
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    Study on four cross combinations based on Jinhua pigs, six white pigs, Landrace pigs and Barkshire pigs
    LU Fuzeng, XU Ruhai, CHU Xiaohong, DAI Lihe, YANG Nana, SHEN Anyu, JIANG Yiquan, GUO Yong
    2019, 31(1):  69-73.  DOI: 10.3969/j.issn.1004-1524.2019.01.09
    Abstract ( 538 )   HTML ( 1 )   PDF (1014KB) ( 1442 )  
    Performance of breeding, growth, slaughter and meat quality of four hybrid pigs were studied with Jinhua pig and six white pig as female parent, Landrace and Berkshire pig as male parent. The results showed that the indexes of Landrace×Jinhua hybrid pigs, inculding number of born alive(12.51), daily weight gain (510.38 g·d-1), feed to gain ratio (3.52), lean meat rate (60.27%), backfat thickness (27.32 mm), skin thickness (3.11 mm), armbling score (2.85), average shearing force (15.64 N), crude protein (260 mg·g-1) were significantly superior to other hybrid combinations. Through performance measurement of four hybrid pigs, the Landrace×Jinhua hybrid pig was selected as the best commodity substitute, which provided scientific basis for its application in the farm.
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    Research and development of primer and probe for identification of porcine-derived materials inferred from TaqMan PCR
    GUO Liang, LI Chundong, XU Weiliang, GUO Yuansheng
    2019, 31(1):  74-79.  DOI: 10.3969/j.issn.1004-1524.2019.01.10
    Abstract ( 462 )   HTML ( 0 )   PDF (1250KB) ( 1401 )  
    The objective of this study was to design the primer and probe with intellectual property which can be used to detect porcine-derived materials by means of TaqMan PCR. The results showed that the technique based on the primers and probe was specific for species identification and quantification, and was able to detect 1 pg template. This biotechnological method based on TaqMan PCR was appropriate to identify porcine-derived materials in farm products and foods.
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    Horticultural Science
    Cloning and expression analysis of β-carotene hydroxylase gene from kale (Brassica oleracea L. var. acephala)
    WANG Yushu, WANG Huan, GUO Yu, ZHOU Minghui, CHEN Lu, CHEN Yang
    2019, 31(1):  80-85.  DOI: 10.3969/j.issn.1004-1524.2019.01.11
    Abstract ( 533 )   HTML ( 0 )   PDF (1163KB) ( 1523 )  
    The β-carotene hydroxylase gene from kale (Brassica oleracea L. var. acephala) was cloned by homology-based cloning and RT-PCR strategies, named as BoBCH(GenBank accession number: MH016242). Sequence analysis showed that the full-length of BoBCH cDNA was 906 bp, which encoded a protein with 301 amino acids, an estimated molecular weight was 33.8 ku and an isoelectric point was 9.67. The results of conservative structural domain analysis showed that BoBCH belonged to the FA_hydroxylase protein superfamily. Phylogenetic tree analysis revealed that the kale had the closest evolutionary relationship with Brassica oleracea. Subcellular localization analysis of TMHMM and Wolf-Psort showed that it might be targeted to the chloroplast with four transmembrane regions. The qRT-PCR test results indicated that the highest was leaf, the next was stem, and the lowest level was in root; in the different periods of leaves, the expression level in the ornamental period was high, and the expression level was lower in seedling stage and rosette stage.
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    Cloning and sequence analysis of two ARF genes and two Aux/IAA genes in Agapanthus praecox ssp. orientalis
    YANG Zhou, LYU Ke, LYU Shan, WANG Junjie, ZHANG Di
    2019, 31(1):  86-97.  DOI: 10.3969/j.issn.1004-1524.2019.01.12
    Abstract ( 536 )   HTML ( 1 )   PDF (4375KB) ( 1690 )  
    Using the Illumina sequencing platform, transcriptome sequencing of Agapanthus praecox ssp. orientalis callus and embryonic callus treated with different concentrations of exogenous auxin picloram (PIC) were performed. Two ARF genes and two Aux/IAA genes that expressed differentially during the auxin signal transduction pathway were obtained and named as ApARF1, ApARF2, ApAux/IAA2 and ApAux/IAA3. To further understand their function in auxin signal transduction during somatic embryogenesis, their full-length cDNA sequences were cloned by RACE technique. The full-length cDNA sequences of ApARF1, ApARF2, ApAux/IAA2 and ApAux/IAA3 were 2 343, 2 888, 1 034 and 821 bp, each contained an open reading frame of 1 770, 2 349, 480 and 549 bp, respectively, which encoded 589, 782, 159 and 182 amino acids, respectively. Through bioinformatic analysis including protein domain analysis, phylogenetic tree analysis, and protein homology analysis, we concluded that ApARF1 and ApARF2 proteins had the typical construction of ARFs, and might be related to plant aging; ApAux/IAA2 lacked a completed domain Ⅳ, ApAux/IAA3 lacked a completed domain Ⅱ; however, they may still have the typical function of Aux/IAA family. We constructed gene over-expression vectors with pHB vector and transformed them into wild-type Arabidopsis thaliana. The phenotypic results showed that compared with the wide-type, the over-expression of ApARF1 and ApARF2 could promote the growth and flowering of transgenic plants, while the over-expression of ApAux/IAA2 and Aux/IAA3 showed a depressing influence on the growth of transgenic plants. The transgenic results combined with the sequence analysis proved that ApARFs and ApAux/IAAs had a regulatory role in auxin signal transduction pathway and plant growth.
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    Plant Protection
    Gene cloning,homology and expression analysis of TaeEF1β in Triticum aestivum L.
    CHEN Xuan, ZHANG Tianye, YANG Jian, ZHANG Hengmu, CHEN Jianping
    2019, 31(1):  98-103.  DOI: 10.3969/j.issn.1004-1524.2019.01.13
    Abstract ( 467 )   HTML ( 3 )   PDF (1832KB) ( 1468 )  
    Eukaryotic translation elongation factor (eEFs) is an important multifunctional protein. eEF1β was subunit of the eukaryotic translation elongation factor-1 (eEFs-1) complex and played an important role in protein biosynthesis. The eEF1β gene was obtained by cloning with RT-PCR from wheat and named as TaeEF1β. The amino acid sequences of TaeEF1β were highly conserved and the conserved domain was located in 137-226 aa. The results of qRT-PCR showed that TaeEF1β were up-regulated in the CWMV-infected plants. In this study, the expression of TaeEF1β in the stems, leaves and roots of wheat and different stages of CWMV infection was also detected by qRT-PCR.
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    Bioinformatics analysis of odorant-binding proteins and chemosensory proteins of Pieris rapae
    ZHU Yu, LIU Yang
    2019, 31(1):  104-112.  DOI: 10.3969/j.issn.1004-1524.2019.01.14
    Abstract ( 375 )   HTML ( 1 )   PDF (10450KB) ( 1346 )  
    Odorant-binding proteins (OBPs) and chemosensory proteins (CSPs) play an important role in the recognition of odors. The putative OBPs and CSPs protein sequences were found in the cabbage butterfly genome by the local BLAST method. We identified 24 PrOBPs and 38 PrCSPs genes using multiple sequence alignments, cysteine pattern sequence recognition, and evolutionary tree construction. Among them, the 17 OBPs of PrOBP1-PrOBP17 belonged to the Classic OBPs protein family, and the other six OBPs, PrOBP19-PrOBP24, belonged to the Minus-C OBPs protein family. All 38 PrCSPs identified had cysteine pattern recognition sequences of typical lepidoptera CSPs. In this paper, the search and identification of OBPs and CSPs genes in the cabbage butterfly genome enriched the database of insect OBPs and CSPs genes, and also provided references for odor identification and chemical sensing experiments and applications of Pieris rapae.
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    Environmental Science
    Changes of soil organic carbon and relationships with soil properties in rice-crayfish coculture system
    GUAN Qinzhuang, CHENG Yongxu, LI Cong, WANG Haifeng, CHEN Huangen, LI Jiayao
    2019, 31(1):  113-120.  DOI: 10.3969/j.issn.1004-1524.2019.01.15
    Abstract ( 535 )   HTML ( 0 )   PDF (1063KB) ( 1613 )  
    A field experiment on rice-crayfish coculture was conducted to assess the influence on soil organic carbon in paddy field with regular rice monoculture as control. Pearson correlation analysis was introduced to explore the relationships within organic carbon, soil fertility and soil enzyme activities. It was shown that rice-crayfish coculture significantly (P<0.05) increased the contents of soil organic matter, but the soil organic carbon contents were significantly (P<0.05) decreased in rice-crayfish coculture with low C/N diet. Under rice-crayfish coculture, soil total phosphorus, soil urease showed significant (P<0.05) positive correlation with soil organic carbon, yet soil cellulose and soil organic matter showed significant negative correlation with soil organic carbon at P<0.01 and P<0.05, respectively. Soil ammonia nitrogen was significantly (P<0.05) negatively correlated with soil organic matter, yet soil cellulose was significantly (P<0.05) positively correlated with soil organic matter.
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    Microbial ecological process of polluted urban river purified by Iris tectorum combined with immobilized bacteria
    LIU Zongnan, WANG Xin, WU Yifei, YAO Xiaohong, SUN Hong, SHEN Qi, LI Weilin, TANG Jiangwu
    2019, 31(1):  121-129.  DOI: 10.3969/j.issn.1004-1524.2019.01.16
    Abstract ( 459 )   HTML ( 15 )   PDF (1384KB) ( 1449 )  
    In order to explore the plant-microorganism interaction and coupling effects, high throughput sequencing technique was used to study the dynamic changes of microbial community in the river sewage by the coupling of Iris tectorum and immobilized water purification bacteria. The source water used in the experiment was river sewage. Four experimental groups were set up: Iris tectorum, Iris tectorum and immobilized water purification bacteria, immobilized water purification bacteria, and blank control. The dynamic simulation experiment was carried out in the experimental device by controlling the flow rate. The results demonstrated that, compared with the inflow water, the ammonia nitrogen in the outflow was on a downward trend, and remained stable after 6 days. The removal efficiency of total nitrogen was low. Total organic carbon in the water also presented a downturn trend and remained stable after 3 days. The removal efficiency of chemical oxygen demand was low. The water was rich in bacterial diversity, covering 10 phyla and 67 genera. The bacterial communities presented a dynamic changing function, which was influenced both by Iris tectorum and immobilized water purification bacteria. Ammonia oxidizing functional microorganisms were mainly affiliated in Proteobacteria, with rather low relative abundance in the species of known classifications. Denitrification functional microorganisms mainly focused on 6 genera of Proteobacteria, whose communities also presented a dynamic changing process. The results showed that Iris tectorum and immobilized bacteria had a significant effect on the water purification process, and had a certain synergistic effect on the changes of bacterial community in water body, and the effect of immobilized water purification bacteria was stronger than that of Iris tectorum.
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    Effects of exopolysaccharides of lactic acid bacteria on rice growth and soil physicochemical properties
    ZHANG Wenping, WANG Qing, HUANG Shichen, WU Peijia, CHENG Xin
    2019, 31(1):  130-138.  DOI: 10.3969/j.issn.1004-1524.2019.01.17
    Abstract ( 852 )   HTML ( 10 )   PDF (1191KB) ( 1602 )  
    To explore the application potential of microbial polysaccharides and its regulatory mechanism on crop growth, rice cultivar Zhunliangyou 608 was used to investigate the effects of exopolysaccharides (EPS) from lactic acid bacteria on biological traits of rice seedlings and physicochemical properties of rice rhizosphere soil. It was shown that application of EPS could promote the growth of rice seedlings and improve rhizosphere soil environment, enhance soil structure, improve soil aggregate stability, mitigate soil acidification, increase soil enzyme activities, and improve soil nutrients. Correlation analysis and principal component analysis showed that the mechanism of rice growth promotion by exopolysaccharides was different from that by glucose. The exopolysaccharides of lactic acid bacteria could be used as a new plant growth regulator.
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    Spatial heterogeneity of available potassium in topsoil based on co-Kriging
    JIANG Yefeng, GUO Xi
    2019, 31(1):  139-148.  DOI: 10.3969/j.issn.1004-1524.2019.01.18
    Abstract ( 462 )   HTML ( 2 )   PDF (2218KB) ( 1607 )  
    The spatial heterogeneity of soil available potassium (AK) was quantified by using general statistics combined with geostatistics based on soil data collected from field surveys (0-20 cm) in the formula fertilization project in Wannian County. The results showed that soil AK ranged from 33.46 mg·kg-1 to 164.84 mg·kg-1 with an average of 82.04 mg·kg-1 in the study area, and was in the fourth grade (classification standard of soil nutrients in the second soil surveys) with a coefficient variation of 30.49%. Parent materials, soil group (subgroup and soil family), elevation, pH, and cation exchange capacity (CEC) had significant (P<0.01) effects on the spatial variation of soil AK. The results of cross-validation showed that co-Kriging with auxiliary variables could improve accuracy compared to ordinary Kriging, the more auxiliary variables, the higher the simulation accuracy, and the more detailed spatial heterogeneity description. The spatial distribution map of soil AK could offer scientific basis for local soil AK management and precision agriculture.
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    Food Science
    Dynamics of 5 fungicides residue in grape brewing fermentation process
    ZHANG Lijun, ZHANG Hu, XU Mingfei, LIN Chunmian, WU Huizhen, XU Jie, QIAN Mingrong
    2019, 31(1):  149-154.  DOI: 10.3969/j.issn.1004-1524.2019.01.19
    Abstract ( 668 )   HTML ( 5 )   PDF (1069KB) ( 1781 )  
    The residue of five fungicides (myclobutanil, famoxadone, mandipropamid, propiconazole, difenoconazole) in homemade wine fermentation process was analyzed by high performance liquid chromatography-mass spectrometry/mass spectrometry (HPLC-MS/MS). The effect of adding yeast on fungicides residue was also studied. It was shown that the average recoveries of the determination method ranged in 75.4%-112.5%. Five fungicides showed different degrees of degradation in the first fermentation stage, yet myclobutanil and mandipropamid showed no significant degradation during the fermentation process with yeast addition. The five fungicides residue showed a balanced state during the secondary fermentation stage. Adding yeast during fermentation did not significantly affect the degradation tendency. The residue of five fungicides in grape brewing process was not only related to the brewing process, but also related to the physicochemical properties of the fungicides.
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    Study on sulfamonomethoxine residue in eggs
    XIA Wei, LI Zuguang, YANG Hua, JI Xiaofeng, WANG Jianmei, QIAN Mingrong
    2019, 31(1):  155-160.  DOI: 10.3969/j.issn.1004-1524.2019.01.20
    Abstract ( 617 )   HTML ( 5 )   PDF (985KB) ( 1522 )  
    Eighty layers of 32-week-old laying hens weighing about 1.6 kg were chosen in this experiment. For test groups, the dose of sulfamonomethoxine was set at 159 mg·L-1 (label recommended maximum dose) and 79.5 mg·L-1 in drinking water, respectively. After continuous medication for 5 days, the addition of sulfamonomethoxine in drinking water was stopped and eggs were collected every day. Sulfamonomethoxine residues in egg samples were pretreated with QuEChERS method and quantified by ultra performance liquid chromatography-mass spectrometer/mass spectrometer (UPLC-MS/MS). The results showed that the residual amount of sulfamonomethoxine in 159 mg·L-1 test group was 2 497.3, 220.1, 38.9, 6.0, 1.3, 0.5, 0.1 μg·kg-1 on the 1st, 3rd, 5th, 10th, 16th, 20th, 24th day, respectively. The residues of sulfamonomethoxine in 79.5 mg·L-1 test group were 694.3, 45.2, 15.5, 1.5, 0.1 μg·kg-1 on the 1st, 3rd, 5th, 10th, 16th day, respectively. Sulfamonomethoxine depletion rate in eggs was 0.4-0.6 μg·kg-1·d-1. According to the maximum residue limit (MRL) of sulfamonomethoxine in animal tissue set by China, the residual amount in eggs was lower than MRL on 5th and 3rd day in 159 mg·L-1 and 79.5 mg·L-1 test group, respectively, without drug application. To guarantee food safety, the proposed withdrawal period should be set at more than 5 days if the label recommended maximum dose of sulfamonomethoxine was applied.
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    Review
    CaMV35S promoter and its application and detection in transgenic crops
    TANG Ting, XIE Shilong, ZHU Xuan, XU Junfeng, TANG Jun, WANG Xiaofu
    2019, 31(1):  161-170.  DOI: 10.3969/j.issn.1004-1524.2019.01.21
    Abstract ( 798 )   HTML ( 22 )   PDF (1527KB) ( 1617 )  
    CaMV35S promoter is one of the most important promoter that widely used in plant genetic engineering. It plays a key role in the safety evaluation and detection of transgenic plants. Understanding the origin and development of CaMV35S promoter is the prerequisite for carrying out safety assessment and detection of transgenic plants. In this review, history of CaMV35S promoter and its structure and function were briefly described. Then, application of CaMV35S promoter in transgenic crops and the corresponding detection methods were analyzed and summarized. Finally, aiming at the problems existing in detection of CaMV35S promoter in transgenic crops, it was proposed that in future studies, sequence information and detection data of related transgenic crops should be communicated and shared, meanwhile, data sharing and joint verification should be carried out among various testing institutions or laboratories, so as to establish a relatively uniform standard detection method for CaMV35S promoter.
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