[1]刘兆明,钟小仙,钱晨,等.苏丹草管状分子体外诱导及木质素合成相关酶活力的变化[J].江苏农业学报,2015,(04):846-854.[doi:10.3969/j.issn.1000-4440.2015.04.022]
 LIU Zhao-ming,ZHONG Xiao-xian,QIAN Chen,et al.In vitro induction of tracheary elements of Sorghum sudanense and changes in lignin synthesis related enzymes activities[J].,2015,(04):846-854.[doi:10.3969/j.issn.1000-4440.2015.04.022]
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苏丹草管状分子体外诱导及木质素合成相关酶活力的变化()
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江苏农业学报[ISSN:1006-6977/CN:61-1281/TN]

卷:
期数:
2015年04期
页码:
846-854
栏目:
畜牧兽医·水产养殖
出版日期:
2015-08-31

文章信息/Info

Title:
In vitro induction of tracheary elements of Sorghum sudanense and changes in lignin synthesis related enzymes activities
作者:
刘兆明12钟小仙2钱晨2刘大林1
(1.扬州大学动物科学与技术学院,江苏扬州225009;2.江苏省农业科学院畜牧研究所,江苏南京210014)
Author(s):
LIU Zhao-ming12ZHONG Xiao-xian2QIAN Chen2LIU Da-lin1
(1.College of Animal Science and Technology,Yangzhou University,Yangzhou 225009,China;2.Institute of Animal Science,Jiangsu Academy of Agricultural Sciences,Nanjing 210014,China) 
关键词:
苏丹草管状分子体外诱导木质素合成
Keywords:
sudangrass(Sorghum sudanense)tracheary elementin vitro inductionlignin synthesis
分类号:
S544+.1
DOI:
10.3969/j.issn.1000-4440.2015.04.022
文献标志码:
A
摘要:
为探索C4作物次生细胞壁合成机制,以苏丹草新品系苏牧3号 的胚性愈伤组织为材料,研究了光照、外源植物激素和活性炭对愈伤组织管状分子分化的影响,并对管状分子诱导过程中木质素含量、可溶性酚醛组分含量及其相关酶活力变化进行了分析。结果表明,在每天光照16 h、不含外源植物激素的基本培养基中添加3 g/L活性炭,诱导培养20 d,管状分子分化率最高,为51.97%,管状分子出现的起始时间为诱导培养第4 d;诱导培养21 d时,木质素含量达到最高值 18.11%,与木质素合成相关的酶PAL、CAD活力也同时达到最高值,分别为 5.915 0×10-3〖KG*3〗U/mg、8.366 7×10-2〖KG*3〗U/mg,此后木质素含量和PAL、CAD酶活力均无显著变化;POD活力诱导培养9 d时达到最高值 132.24 U/mg,显著高于继代培养;可溶性酚醛组分含量先增后减,诱导培养12 d时达到最高值 1.09 μg/mg。
Abstract:
To reveal the secondary cell wall synthesis mechanism of C4 crops, the effect of illumination, exogenous hormone and activated carbon concentration on tracheary elements induction in vitro was studied on sudangrass Sumu No.3. The changes of lignin content, soluble phenolic components contents and related enzymes activities were analyzed in the process of tracheary elements induction as well. The results showed that the differentiation rate of tracheary elements reached the highest point (51.97%) at 20th day induction in 16-h daily illumination when calli were cultured in plant hormone-free MS medium with 3 g/L activated carbon addition. After 21-d induction, ligin content get to the peak value of 18.11%, and so did the activities of enzymes PAL (phenylalanine ammonia lyase and CAD (cinnamyl alcohol dehydrogenase, which were shown to be 5.915 0×10-3 U/mg and 8.366 7×10-2〖KG*3〗U/mg, respectively. The lignin content and enzymatic activities did not changed significantly afterwards. The activity of enzyme POD (peroxidase) came to its maximum value of 132.24 U/mg after 12-d induction. Soluble phenolic components content increased over time and reached the highest of 1.09 μg/mg after 12-d induction 12th day, and then decreased.

参考文献/References:


[1]KOHLENBACH H W, SCHMIDT B. Cytodifferenzierung in form einer direkten umwandlung isolierter mesophyllzellen zu tracheiden (Cytodifferentiation in the mode of a direct transformation of isolated mesophyll cells to tracheids) [J]. Z Pflanzenphysiol, 1975, 75:369-374.
[2]FUKUDA H, KOMAMINE A. Establishment of an experimental system for the tracheary element differentiation from single cells isolated from the mesophyll of Zinnia elegans[J]. Plant Physiology, 1980, 65:57-60.
[3]ODA Y, MIMURA T, HASEZAWA S. Regulation of secondary cell wall development by cortical microtubules during tracheary element differentiation in Arabidopsis cell suspensions[J]. Plant Physiology, 2005, 137(3):1027-1036.
[4]BLEE K A,WHERTLEY E R,BONHAM V A,et al. Proteomic analysis reveals a novel set of cell wall proteins in a transformed tobacco cell culture that synthesizes secondary walls as determined by biochemical and morphological parameters[J]. Planta,2001,212:404-415.
[5]MLLER R, MCDONALD A G, WALTER C, et al. Cell differentiation, secondary cell wall formation and transformation of callus tissue of Pinus radiata D. Don[J]. Planta, 2003, 217: 736-747.
[6]OHLSSON A B, DJERBI S, WINZELL A, et al. Cell suspension cultures of Populus tremula ×P. tremuloides exhibit a high level of cellulose synthase gene expression that coincides with increased in vitro cellulose synthase activity[J].Protoplasma, 2006, 228(4): 221-229.
[7]PILLAI K V, MCDONALD A G, WAGNER F G. Developing a model system in vitro to understand tracheary element development in douglas-fir(Pseudostuga menziesii)[J]. Maderas Cienciay Techlolgia, 2011,13 (1): 3-18.
[8]吕淑萍,倪志勇,范玲. 木质素生物合成相关酶基因调控的研究进展[J]. 分子植物育种,2011,75(9): 1545-1555.
[9]MLLER R, KOCH G, NANAYAKKARA B, et al. Lignification in cell cultures of Pinus radiate: activities of enzymes and lignin topochemistry[J].Tree Physiology, 2005, 26: 201-210.
[10]吕宗友,苏衍菁,赵国琦,等. 不同防褐化措施对苏丹草愈伤诱导以及抗褐化的效果研究[J].草业学报, 2011, 20(3):174-181.
[11]刘晨,哈斯亚提·托逊江,热沙来提汗·买买提,等. 香梨与牧草套种对产草量及土壤性状的影响[J]. 江苏农业科学,2013,41(8):209-211.
[12]钟小仙,佘建明,顾洪如,等. 苏丹草幼穗离体培养植物的再生技术[J]. 江苏农业学报, 2005, 21(4):331-335.
[13]KRALIK D, ELTER A M, KUKIC S, et al. Sudan grass-energy crop for biogas production[J]. Krmiva, 2009, 51(3):171-178.
[14]MURASHIGE T, SKOOG F. A revised medium from rapid growth and bioassays with tobacco tissue cultures[J]. Physiology Plant, 1962, 15: 473-497.
[15]GAMBORG O L, MILLER R A, OJIMA K. Nutrient requirements of suspension cultures of soybeanroot cells[J]. Exp Cell Res, 1968, 50: 151-158.
[16]KRISHNAMURTHY K V. Methods in Cell Wall Cytochemistry[M]. Boca Raton :CRC Press,1999.
[17]EDWARDS R A, KESSMANN H. Isoflavonoid phytoalexins: their biosynthetic enzymes[M]. Oxford: Oxford University Press, 1992: 54-55.
[18]WYRAMBIK D, GRISEBACH H. Purification and properties of isoenzymes of cinnamyl-alcohol dehydrogenase from soybean-cell-suspension cultures[J]. European Journal of Biochemistry, 1975, 59(1): 9-15.
[19]MIZUNO K, KOMAMINE A, SHIMOKORIYAMA M. Vessel element formation in cultured carrot-root phloem slices[J]. Plant and Cell Physiology, 1971, 12(6): 823-830.
[20]YEN H E, YEN S K. Effect of high salinity on tracheary element differentiation in light-grown callus of Mesembryanthemum crystallinum[J]. Plant Cell, Tissue and Organ Culture, 1999, 58: 59-65.
[21]MLLER R, BALL R D, HENDERSON A R, et al. Effect of light and activated charcoal on tracheary element differentiation in callus cultures of Pinus radiata D. Don[J]. Plant Cell, Tissue and Organ Culture, 2006, 85: 161-171.
[22]FUKUDA H, KOMAMINE A. Establishment of an experimental system for the study of tracheary element different from single cells isolated from the mesophyll of Zinnia elegans[J].Plant Physiol, 1980, 65(1): 57-60.
[23]SATO Y, YAJIMAa Y, TOKUNAGA N, et al. Comparison between tracheary element lignin formation and extracellular lignin-like substance formation during the culture of isolated Zinnia elegans mesophyll cells[J]. Biologia, 2011, 66 (1): 88-95.
[24]CHURCH D L, GALSTON A W. Hormonal induction and antihormonal inhibition of tracheary element differentiation in Zinnia cell cultures[J]. Phytochemistry, 1988, 27 (8): 2435-2439.
[25]刘根林,梁珍海,朱军. 活性炭在植物组织培养中的作用概述[J]. 江苏林业科技, 2001,28(5):46-48.
[26]YAMAGISHIY, SATO T, UCHIYAMA H, et al. Tracheary elements that resemble secondary xylem in calli derived from the conifers, Torrya nucifera and Cryptomeria japonica[J]. Journal of Wood Science, 2012, 58: 557-562.
[27]田敏,夏琼梅,李纪元. 植物的次生生长及其分子调控[J]. 遗传, 2007, 29(11): 1324-1330.
[28]PETER G, NEALE D. Molecular basis for the evolution of xylem lignification[J]. Curr Opin Plant Biol, 2004, 7: 737-742.
[29]陈永忠,谭晓风,DAVID C. 木质素生物合成及其基因调控研究综述[J].江西农业大学学报, 2003, 25(4):613-617.
[30]KOCH G, KLEIST G. Application of scanning UV micro-spectrophotometry to localise lignins and phenolic extractives in plant cell walls[J]. Holzforschung, 2001,55:563-567.
[31]SATO Y T, WATANABE A, KOMAMINE T, et al. Changes in the activity and mRNA of cinnamyl alcohol dehydrogenase during tracheary element differentiation in Zinnia[J]. Plant Physiology, 1997, 113:425-430.
[32]ZWLIHA I, TIJEN O, AHU A, et al. Reduced leaf peroxidase activity is associated with reduced lignin content in transgenic poplar[J]. Plant Biotechnology, 1999, 16(5): 381-387.〖ZK)〗〖FL)〗

备注/Memo

备注/Memo:
收稿日期:2015-03-26 基金项目:国家牧草产业技术体系综合试验站项目(CARS-35);江苏省农业科技自主创新基金项目[CX(13)3035];江苏省第四期“333工程”培养资金资助项目 作者简介:刘兆明(1990-),男,山东潍坊人,硕士研究生,主要从事牧草育种研究。(Email)lzzm2012@163.com 通讯作者:钟小仙,(Tel)025-84390239 ;(E-mail)zhpansy@aliyun.com
更新日期/Last Update: 2015-08-31