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  • Cloning, structural and function analysis of MiMYB44L gene in kernels of Macadamia integrifolia

    Subjects: Biology >> Botany >> Applied botany submitted time 2024-05-15 Cooperative journals: 《广西植物》

    Abstract: Macadamia nut (Macadamia integrifolia) is an evergreen nut tree with high economic value. Its kernel is rich in nutrients such as fatty acid and protein, etc. In order to further explore the main regulatory genes related to nutrient formation in M. integrifolia kernels, transcriptomics, gene cloning, fluorescence quantification PCR and bioinformatics techniques were used to screen potential regulatory genes from the kernel transcriptomes of ‘Guire No. 1’ and ‘A4’, which have significantly different nutrient content in M. integrifolia kernels. The results were as follows: (1) Transcriptome analysis showed that 1 667 genes were up-regulated and 1 798 genes down-regulated in ‘Guire No. 1’ kernel compared with those of ‘A4’ kernel and KEGG enrichment analysis showed that the differential genes were mainly in starch and glucose metabolism, amino acid biosynthesis and carbon metabolism. (2) A significant differential gene-LOC122077931 encoding the R2R3-MYB transcription factor MYB44L was discovered. The MiMYB44L gene was cloned in kernels of M. integrifolia variety ‘Guire No. 1’ using RACE technology, which was 1 165 bp in length, 999 bp in ORF in length, and encoded 332 amino acids. (3) Bioinformatics analysis confirmed the presence of the SANT domain in the MiMYB44L protein, a hallmark feature of the R2R3-MYB family. The protein lacked both a signal peptide and a transmembrane domain but featured phosphorylation sites. (4) The protein content in kernels of 10 M. integrifolia varieties was determined. And it was found that the expression of MiMYB44L gene in M. integrifolia varieties with high protein content was significantly higher than that in varieties with low protein content, and the overall correlation coefficient was 0.54, reaching a very significant level. The results of this study provide theoretical guidance for in-depth analysis of the regulatory mechanism of MiMYB44L gene in the formation of protein content in M. integrifolia.

  • 共轭亚油酸对开产蛋鸡生产性能、蛋品质、蛋黄硬度和蛋黄脂肪酸组成的影响

    Subjects: Biology >> Zoology submitted time 2018-12-24 Cooperative journals: 《动物营养学报》

    Abstract:本试验旨在研究饲粮添加共轭亚油酸(CLA)对开产蛋鸡生产性能、蛋品质、蛋黄硬度和蛋黄脂肪酸组成的影响。采用单因素随机试验设计,选用产蛋率、体重相近的18周龄海兰褐蛋鸡630只,随机分为7组,每组6个重复,每个重复15只鸡,分别饲喂添加0、1%、2%、3%、4%、5%和6% CLA的试验饲粮,预试期1周,正试期8周。结果表明:1)饲粮CLA添加水平≤2%时,对蛋鸡的生产性能、蛋品质无显著影响(P>0.05)。与对照组相比,饲粮添加2%~4% CLA可增加蛋壳厚度(P>0.05);饲粮CLA添加水平≥3%时,产蛋率显著降低(P<0.05),蛋黄硬度显著增加(P<0.05);饲粮CLA添加水平≥4%时,平均日采食量和腹脂率显著降低(P<0.05);饲粮CLA添加水平≥5%时,料蛋比显著升高(P<0.05),蛋黄比例显著降低(P<0.05)。2)1%、2% CLA添加组蛋黄中C16:0、C18:0和饱和脂肪酸(SFA)含量显著低于其他组(P<0.05)。与对照组相比,饲粮CLA添加水平≥4%时,蛋黄中C16:0、C18:0和SFA含量显著增加(P<0.05),C16:1、C18:1、单不饱和脂肪酸(MUFA)和多不饱和脂肪酸(PUFA)含量显著降低(P<0.05)。蛋黄中CLA含量随饲粮CLA添加水平的增加呈显著二次升高(P<0.01),c9,t11-CLA的富集量是t10,c12-CLA的1.47倍。综上,饲粮添加2% CLA,可以改善蛋壳质量,降低蛋黄中SFA含量,蛋黄中可富集一定量的CLA,且不影响蛋鸡的生产性能和蛋品质。

  • 饲粮添加亮氨酸和谷氨酸对肥育猪肌肉脂肪酸组成和脂质代谢相关基因表达的影响

    Subjects: Biology >> Zoology submitted time 2018-12-24 Cooperative journals: 《动物营养学报》

    Abstract:本试验旨在探讨饲粮添加亮氨酸和谷氨酸对肥育猪肌肉脂肪酸组成和脂质代谢相关基因表达的影响。选取平均体重为77 kg左右的三元杂交肥育猪60头,随机分为5个组,每组12头,公、母各占1/2。对照组饲喂基础饲粮,试验组分别在基础饲粮中添加2.05% L-丙氨酸(等氮对照组)、1.0%亮氨酸+1.37% L-丙氨酸(亮氨酸组)、1.0%谷氨酸+1.44% L-丙氨酸(谷氨酸组)、1.0%亮氨酸+1.0%谷氨酸(亮氨酸+谷氨酸组)。饲喂60 d后屠宰采集肌肉样品,检测其中脂肪酸含量以及脂质代谢相关基因mRNA的相对表达量。结果表明:与对照组相比,在背最长肌中,亮氨酸组C18:2n-6和C20:1含量显著增加(P<0.05),C18:0含量显著降低(P<0.05),谷氨酸组C14:0和C16:0含量显著降低(P<0.05),C17:0和C18:2n-6含量显著增加(P<0.05);在股二头肌中,亮氨酸组C16:0含量显著降低(P<0.05),谷氨酸组C18:2n-6含量显著增加(P<0.05)。与对照组相比,亮氨酸组背最长肌中脂肪酸转运蛋白1(FATP-1)mRNA的相对表达量显著上调(P<0.05),亮氨酸+谷氨酸组背最长肌和股二头肌中脂肪酸转运蛋白4(FATP-4)mRNA的相对表达量表达显著下调(P<0.05)。与等氮对照组相比,谷氨酸组和亮氨酸+谷氨酸组背最长肌中脂蛋白脂酶(LPL)mRNA的相对表达量显著上调(P<0.05)。上述结果提示,饲粮添加1.00%亮氨酸或1.00%谷氨酸可调控肥育猪肌肉中脂肪酸组成及脂质代谢相关基因的表达。

  • 不同来源木聚糖酶及其组合对肉鸡肠道黏膜形态与二糖酶活性及其基因表达的影响

    Subjects: Biology >> Zoology submitted time 2018-12-24 Cooperative journals: 《动物营养学报》

    Abstract:本试验旨在探讨不同来源木聚糖酶及其组合对黄羽肉鸡肠道黏膜形态、二糖酶活性及其基因表达的影响。试验选取1 560只1日龄黄羽肉公鸡,随机分为4组(每组6个重复,每个重复65只):对照组(Ⅰ组)饲喂低能量低蛋白质的基础饲粮,试验组(Ⅱ、Ⅲ和Ⅳ组)分别饲喂在基础饲粮中添加4 000 U/kg的黑曲霉来源单一木聚糖酶1#、康氏木霉来源单一木聚糖酶2#和组合型木聚糖酶(木聚糖酶1#:木聚糖酶2#=1:1)的饲粮,试验期63 d。每个重复分别于21、42和63日龄时取2只肉鸡采集肠道组织,用于肠道黏膜形态、二糖酶活性及二糖酶基因mRNA表达丰度的测定。结果表明:1)Ⅳ组21日龄时空肠隐窝深度显著低于Ⅰ组(P<0.05);Ⅳ组42日龄时十二指肠绒毛高度/隐窝深度(V/C)值极显著大于Ⅰ组(P<0.01),显著大于Ⅱ和Ⅲ组(P<0.05),且Ⅳ组42日龄时空肠V/C值极显著大于Ⅰ、Ⅱ和Ⅲ组(P<0.01)。2)21日龄时,十二指肠和空肠中麦芽糖酶活性以及空肠中蔗糖酶活性表现为Ⅳ组极显著高于Ⅰ、Ⅱ和Ⅲ组(P<0.01);42日龄时,空肠中蔗糖酶活性表现为Ⅳ组极显著高于Ⅰ和Ⅱ组(P<0.01),显著高于Ⅲ组(P<0.05)。3)42日龄时,Ⅳ组空肠中麦芽糖酶-葡萄糖淀粉酶(MGA)mRNA表达丰度极显著高于Ⅰ和Ⅱ组(P<0.01)。由此得出,肉鸡在前(1~21日龄)、中期(22~42日龄)阶段,木聚糖酶的添加能够改善肉鸡肠道黏膜形态,促进二糖酶的分泌及其基因表达,且组合型木聚糖酶的作用效果优于单一木聚糖酶,表现出高效催化的组合效应

  • 饲料中添加低聚木糖对仿刺参幼参生长性能、肠道消化酶活力和免疫力的影响

    Subjects: Biology >> Zoology submitted time 2017-10-23 Cooperative journals: 《动物营养学报》

    Abstract:在水温14.8~18.6 ℃、盐度(29±1) PSU下,用120 L的蓝色塑钢水箱研究了饲料中添加低聚木糖(xylo-oligosaccharides,XOS)对仿刺参(Apostichopus japonicus Selenka)幼参生长性能、肠道消化酶活力和免疫力的影响。配制XOS添加量分别为0(对照)、0.015%、0.030%、0.045%、0.060%和0.075%的6组试验饲料,投喂平均体重为(6.80±1.05) g的仿刺参幼参75 d。每组饲料随机投喂3个水箱,每个水箱放养45头幼参。结果显示:饲料中添加XOS显著提高了仿刺参幼参的特定生长率(SGR)(P0.05)。饲料中添加XOS提高了仿刺参幼参的干物质表观消化率(ADDM),但仅0.030%组显著高于对照组(P0.05)。由此得出,饲料中添加0.030%~0.060%的XOS可提高仿刺参幼参肠道消化酶活力,增强其免疫力,从而促进仿刺参幼参生长;仿刺参饲料中XOS的最适添加量为0.044%,建议XOS投喂时间在2个月左右。