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Tomato arabinosyltransferase prevents precocious senescence
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作者 Ho-Young Jeong Yoonseo Lim +4 位作者 Myeong-Gyun Seo Soon Ju Park Chanhui Lee Young-Joon Park Choon-Tak Kwon 《Horticultural Plant Journal》 2025年第4期1583-1594,共12页
Senescence,a crucial developmental process in the life cycle of plants,involves programmed destruction of cellular components of leaves.The onset of senescence is synchronized with other developmental processes for su... Senescence,a crucial developmental process in the life cycle of plants,involves programmed destruction of cellular components of leaves.The onset of senescence is synchronized with other developmental processes for successful reproduction since senescence eventually leads to cell death.Arabinosyltransferase FASCIATED AND BRANCHED 2(FAB2)is known to control meristem proliferation.Here,we show that FAB2 could inhibit premature leaf senescence in tomato plants.Both chemically mutagenized and CRISPR-generated fab2 mutants exhibited excessively accelerated senescence,which resulted in sterility.Transcriptome analysis revealed that FAB2 extended leaf longevity by suppressing transcription of genes highly expressed in mature leaves.Transcription of FAB2 was increased in younger leaves,potentially inhibiting premature leaf senescence.The precocious senescence of fab2 mutants was in contrast to fasciated inflorescence(fin)mutants,which carried mutations in a hydroxyproline O-arabinosyltransferase gene,leading to meristem overproliferation.Our observations indicate that complex genetic hierarchy in the cascade of tomato arabinosyltransferases could control different aspects of developmental processes such as stem cell proliferation and senescence. 展开更多
关键词 Arabinosyltransferase Leaf senescence CRISPR fab2 Transcriptome analysis
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三步法制备级纯化抗CD20(Fab′)_2
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作者 王金宏 杨铭 +3 位作者 范冬梅 许元生 熊冬生 杨纯正 《中国医学科学院学报》 CAS CSCD 北大核心 2008年第5期622-625,共4页
目的在小规模蛋白纯化系统AKTA prime上建立制备级纯化抗CD20(Fab′)2的方法。方法将通过高渗溶液提取的周质腔蛋白抗CD20(Fab′)2依次经过离子柱、疏水柱和亲和柱纯化,采用蛋白电泳和高效液相色谱法分析检测其分离效果及纯度,同时测定... 目的在小规模蛋白纯化系统AKTA prime上建立制备级纯化抗CD20(Fab′)2的方法。方法将通过高渗溶液提取的周质腔蛋白抗CD20(Fab′)2依次经过离子柱、疏水柱和亲和柱纯化,采用蛋白电泳和高效液相色谱法分析检测其分离效果及纯度,同时测定其与Raji细胞的结合活性。结果在该纯化条件下一次可获得8mg纯度为96.678%的抗CD20(Fab′)2,其与CD20+Raji细胞的结合活性与采用亲和柱联合分子筛柱得到的抗体活性基本一致。结论三步法制备级纯化抗CD20(Fab′)2操作简单,能获得制备级高纯度抗CD20(Fab′)2。 展开更多
关键词 抗CD20(Fab′)2 三步法纯化 高效液相色谱分析
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