Welcome to Acta Agronomica Sinica,

Acta Agronomica Sinica ›› 2020, Vol. 46 ›› Issue (02): 166-178.doi: 10.3724/SP.J.1006.2020.84086

• CROP GENETICS & BREEDING·GERMPLASM RESOURCES·MOLECULAR GENETICS • Previous Articles     Next Articles

Cloning and expression analysis of metallothionein family genes in response to heavy metal stress in sugarcane (Saccharum officinarum L.)

GAO Shi-Wu1,FU Zhi-Wei1,CHEN Yun1,LIN Zhao-Li2,XU Li-Ping1,GUO Jin-Long1,*()   

  1. 1 Key Laboratory of Sugarcane Biology and Genetic Breeding (Fujian), Ministry of Agriculture and Rural Affairs / Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, China
    2 Sugarcane and Products Quality Supervisory Inspection and Test Center of Ministry of Agriculture and Rural Affairs / Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, China
  • Received:2019-06-10 Accepted:2019-09-26 Online:2020-02-12 Published:2019-10-14
  • Contact: Jin-Long GUO E-mail:jl.guo@163com
  • Supported by:
    This study was supported by the National Natural Science Foundation of China(31871690);the Foundation for China Scholarship Council(20163035)

Abstract:

Metallothioneins (MTs) are cysteine-rich, low-molecular-weight proteins. Plant MTs play important roles in detoxi?cation and cellular redox regulation. In this study, hydroponic experiments of sugarcane (Saccharum officinarum L. cv. Badila) were carried out to study the effects of CdCl2, ZnSO4, and CuCl2 treatments on plantlet growth. And then three kinds of heavy metal content in both shoots and roots of sugarcane were detected, showing an enrichment and tolerance ability to Cd 2+, Zn 2+, and Cu 2+ in Badila seedlings. Three metallothionein genes, termed as ScMT1 (accession number: KJ504373), ScMT2-1-5 (accession number: MH191346), and ScMT3 (accession number: KJ5043704), were isolated from Badila. ScMT1 contained an open reading frame (ORF) of 228 bp encoding 75 amino acids residues. The first (52 bp) and second (176 bp) extrons of ScMT1 were separated by an intron (283 bp). ScMT2-1-5 contained an ORF of 246 bp encoding 81 amino acids residues. The first (64 bp), second (87 bp), and third (101 bp) extrons of ScMT2-1-5 were separated by two introns (483 bp and 853 bp). ScMT3 contained an ORF of 198 bp encoding 65 amino acids residues. The first (50 bp) and second (148 bp) extrons of ScMT3 were separated by an intron (259 bp). The deduce protein ScMT1, ScMT2-1-5, and ScMT3 were categorized into the subfamily of plant type1, type2, and type3 MTs, respectively. The expression profiles of the three genes under different heavy-metal stresses were investigated by real-time quantitative PCR (qRT-PCR) analysis. When treated with Cd 2+, the expression of ScMT2-1-5 was continuously and significantly up-regulated in both shoots and roots, while that of ScMT1 showed a delayed up-regulation pattern. The expression of ScMT3 showed a delayed up-regulation pattern in shoots and a trend of first raising and then suppressing in roots. The results suggested that ScMT2-1-5 might play a more active role in response to Cd 2+in sugarcane while ScMT3 might not, and ScMT1 is involved in the molecular responses of Cd 2+ stress at the later stage. When treated with Cu 2+, the expression of ScMT1 was continuously and significantly up-regulated, and that of ScMT2-1-5 and ScMT3 general up-regulated in shoots. As in the roots, the expression of both ScMT1 and ScMT2-1-5 showed a delayed up-regulation pattern which was significantly up-regulated at the later stage, while that of ScMT3 significantly up-regulated at the early stage. It revealed that ScMT1 cooperated with ScMT2-1-5 and ScMT3 is involved in the positive response to Cu 2+ stress in roots, and might play a more positive role than ScMT2-1-5 and ScMT3, and the three genes are successively involved in the molecular responses of Cu 2+ stress in roots. When treated with Zn 2+, the expression of ScMT1 and ScMT3 increased only in shoots and roots, respectively. The expression of ScMT2-1-5 was up-regulated at the early stage and then suppressed in both shoots and roots. It suggests that ScMT1 and ScMT3 mainly function in shoots and roots, respectively, when exposed to Zn 2+ stress. ScMT2-1-5 was involved in the molecular responses of Cd 2+ stress at the early stage. ScMT1, ScMT2-1-5, and ScMT3 showed similar or complementary expression patterns in different tissues of sugarcane when exposed to heavy metals, which revealed the functional diversity of sugarcane MTs in detoxi?cation and cellular redox regulation, and their spatiotemporal coordination in mitigating or even preventing tissue injury caused by excessive heavy metals. The results provide a basic information for further research on mechanisms in the synergistic enhancement of tolerance to heavy metals for MTs family genes in the highly polyploid sugarcane.

Key words: sugarcane (Saccharum officinarum L.), metallothionein, heavy metal, real-time qPCR

Table 1

Primers for isolation of sugarcane metallothionein genes"

基因
Gene
上游引物
Forward primer (5°-3°)
下游引物
Reverse primer (5°-3°)
ScMT1 TGTAACACGCCCTTTGGTAGAT TGTCCTTATTGTTCAACCACCAG
ScMT2-1-5 CGAGGAGAGGAAGAGGACGACT TTATTCGTTCCCATCAGTACCA
ScMT3 AAGAAGGCCTTGCGCAACAAA ACGTACCGCGTCAGGTCCTCGT

Table 2

qPCR primers for amplification of sugarcane metallothionein genes"

基因
Gene
上游引物
Forward primer (5°-3°)
下游引物
Reverse primer (5°-3°)
ScMT1 TGTAACACGCCCTTTGGTAGAT CTCCTCCAGGTCAGGGTACTTC
ScMT2-1-5 GAGGAAGAGGACGACTGCGAGG TCATCGCCAC CTCCTCACTT
ScMT3 GCTTCCAGCATGTCGGGCAC ACGGTCACCTCCTCCTCAACGA
GAPDH CACGGCCACTGGAAGCA TCCTCAGGGTTCCTGATGCC

Fig. 1

Phenotype of sugarcane seedlings treated with heavy metals for 48 h A: CK; B; CdCl2; C: ZnSO4; D: CuCl2."

Fig. 2

Heavy metal contents in sugarcane shoots and roots under the stresses of Cd2+, Zn2+, or Cu2+ Bars superscripted by different letters are significantly different at the 5% probability level."

Fig. 3

Agarose electrophoresis analysis of the RT-PCR products of ScMTs M: DNA ladder marker; 1: ScMT1; 2: ScMT2-1-5; 3: ScMT3."

Fig. 4

Nucleotide sequence and deduced amino acid sequence for ScMTs A: ScMT1; B: ScMT2-1-5; C: ScMT3. *: Terminal codon; C shows the conservative cysteine residual of Cys-rich domain."

Fig. 5

Phylogenetic relationships of MTs and a schematic diagram of the exon/intron structures of the MT genes from Saccharum spp., Oryza sativa L., and Arabidopsis thaliana L. Boxes and lines indicate exons and introns, respectively."

Fig. 6

Expression patterns of ScMT1 in sugarcane under different heavy metal stresses A, C, and E represent the expression patterns of ScMT1 in response to CdCl2, ZnSO4, and CuCl2, respectively. B, D, and F represent the ratio of ScMT1 expression level between treatment (CdCl2, ZnSO4, and CuCl2, respectively) and their control groups. The error bars represent the standard errors of each treating group (n = 3). Bars superscripted by different letters are significantly different at the 5% probability level."

Fig. 7

Expression patterns of ScMT2-1-5 in sugarcane under different heavy metal stresses A, C, and E represent the expression patterns of ScMT2-1-5 in response to CdCl2, ZnSO4, and CuCl2, respectively. B, D, and F represent the ratio of ScMT2-1-5 expression level between treatment (CdCl2, ZnSO4, and CuCl2, respectively) and their control groups. The error bars represent the standard errors of each treating group (n = 3). Bars superscripted by different letters are significantly different at the 5% probability level."

Fig. 8

Expression patterns of ScMT3 in sugarcane under different heavy metal stresses A, C, and E represent the expression patterns of ScMT3 in response to CdCl2, ZnSO4, and CuCl2, respectively. B, D and F represent the ratio of ScMT3 expression level between treatment (CdCl2, ZnSO4, and CuCl2, respectively) and their control groups. The error bars represent the standard errors of each treating group (n = 3). Bars superscripted by different letters are significantly different at the 5% probability level."

[1] Cobbett C, Goldsbrough P . Phytochelatins and metallothioneins: roles in heavy metal detoxification and homeostasis. Annu Rev Plant Biol, 2002,53:159-182.
doi: 10.1146/annurev.arplant.53.100301.135154 pmid: 12221971
[2] 常团结, 朱祯 . 植物金属硫蛋白研究进展(一) ——植物MT的分类、特征及其基因结构. 生物技术通报, 2002, ( 3):5-10.
Chang T J, Zhu Z . Study advances of plant metallothionein ——classification, characteristics and gene structure. Biotechnol Bull, 2002, ( 3):5-10 (in Chinese with English abstract).
[3] 全先庆, 张洪涛, 单雷, 毕玉平 . 植物金属硫蛋白及其重金属解毒机制研究进展. 遗传, 2006,28:375-382.
Quan X Q, Zhang H T, Shan L, Bi Y P . Advances in plant metallothionein and its heavy metal detoxification mechanisms. Hereditas (Beijing), 2006,28:375-382 (in Chinese with English abstract).
[4] Ziller A, Yadav R K, Capdevila M, Reddy M S, Vallon L, Marmeisse R, Atrian S, Palacios Ò, Fraissinet-Tachet L . Metagenomics analysis reveals a new metallothionein family: Sequence and metal-binding features of new environmental cysteine-rich proteins. J Inorg Biochem, 2017,167:1-11.
doi: 10.1016/j.jinorgbio.2016.11.017 pmid: 27886631
[5] Akashi K, Nishimura N, Ishida Y, Yokota A . Potent hydroxyl radical-scavenging activity of drought-induced type-2 metallothionein in wild watermelon. Biochem Biophys Res Commun, 2004,323:72-78.
doi: 10.1016/j.bbrc.2004.08.056 pmid: 15351703
[6] Wong H L, Sakamoto T, Kawasaki T, Umemura K, Shimamoto K . Down-regulation of metallothionein, a reactive oxygen scavenger, by the small GTPase OsRac1 in rice. Plant Physiol, 2004,135:1447-1456.
doi: 10.1104/pp.103.036384 pmid: 15220467
[7] Haq F, Mahoney M, Koropatnick J . Signaling events for metallothionein induction. Mutat Res, 2003,533:211-226.
doi: 10.1016/j.mrfmmm.2003.07.014 pmid: 14643422
[8] Fabisiak J P, Borisenko G G, Liu S X, Tyurin V A, Pitt B R, Kagan V E . Redox sensor function of metallothioneins. Methods Enzymol, 2001,353:268-281.
doi: 10.1016/s0076-6879(02)53055-x pmid: 12078502
[9] Vašák M, Hasler D W . Metallothioneins: new functional and structural insights. Curr Opin Chem Biol, 2000,4:177-183.
doi: 10.1016/s1367-5931(00)00082-x pmid: 10742189
[10] Freisinger E . Structural features specific to plant metallothioneins. J Biol Inorg Chem, 2011,16:1035-1045.
doi: 10.1007/s00775-011-0801-z pmid: 21688177
[11] Grennan A K . Metallothioneins, a diverse protein family. Plant Physiol, 2011,155:1750-1751.
doi: 10.1104/pp.111.900407 pmid: 21459979
[12] Leszczyszyn O I, Imam H T, Blindauer C A . Diversity and distribution of plant metallothioneins: a review of structure, properties and functions. Metallomics, 2013,5:1146-1169.
doi: 10.1039/c3mt00072a
[13] Schiller M, Hegelund J N, Pedas P, Kichey T, Laursen K H, Husted S, Schjoerring J K . Barley metallothioneins differ in ontogenetic pattern and response to metals. Plant Cell Environ, 2014,37:353-367.
doi: 10.1111/pce.12158
[14] Kumar G, Kushwaha H R, Panjabi-Sabharwal V, Kumari S, Joshi R, Karan R, Mittal S, Pareek S L, Pareek A . Clustered metallothionein genes are co-regulated in rice and ectopic expression of OsMT1e-P confers multiple abiotic stress tolerance in tobacco via ROS scavenging. BMC Plant Biol, 2012,12:107.
doi: 10.1186/1471-2229-12-107 pmid: 22780875
[15] Sereno M L, Almeida R S, Nishimura D S, Figueira A . Response of sugarcane to increasing concentrations of copper and cadmium and expression of metallothionein genes. J Plant Physiol, 2007,164:1499-1515.
doi: 10.1016/j.jplph.2006.09.007 pmid: 17175063
[16] Figueira A, Kido E A, Almeida R S . Identifying sugarcane expressed sequences associated with nutrient transporters and peptide metal chelators. Genet Mol Biol, 2001,24:207-220.
doi: 10.1590/S1415-47572001000100028
[17] Guo J, Xu L, Su Y, Wang H, Gao S, Xu J, Que Y . ScMT2-1-3, a metallothionein gene of sugarcane, plays an important role in the regulation of heavy metal tolerance/accumulation. Biomed Res Int, 2013. doi: 10.1155/2013/904769.
doi: 10.1155/2019/3401505 pmid: 31886774
[18] 陈云, 王竹青, 傅志伟, 杨玉婷, 郭晋隆, 苏亚春, 许莉萍 . 甘蔗金属硫蛋白基因(ScMT2-1-4)的克隆及表达分析. 基因组学与应用生物学, 2015,34:357-364.
Chen Y, Wang Z Q, Fu Z W, Yang Y T, Guo J L, Su Y C, Xu L P . Cloning and expression analysis of metallothionein gene ScMT2-1-4 in Sugarcane. Genom Appl Biol, 2015,34:357-364 (in Chinese with English abstract).
[19] Verma A K, Agarwal A K, Dubey R S, Solomon S, Singh S B . Sugar partitioning in sprouting lateral bud and shoot development of sugarcane. Plant Physiol Biochem, 2013,62:111-115.
doi: 10.1016/j.plaphy.2012.10.021 pmid: 23208305
[20] D’hont A, Grivet L, Feldmann P, Rao S, Berding N, Glaszmann J C . Characterisation of the double genome structure of modern sugarcane cultivars (Saccharum spp.) by molecular cytogenetics. Mol Gen Genet, 1996,250:405-413.
doi: 10.1007/bf02174028 pmid: 8602157
[21] Edmé S J, Comstock J C, Miller J D, Tai P Y P . Determination of DNA content and genome size in sugarcane. J Am Soc Sugar Cane Technol, 2005,25:1-16.
doi: 10.1038/s41467-018-05051-5 pmid: 29980662
[22] Zhang J, Nagai C, Yu Q, Pan Y B, Ayala-Silva T, Schnell R J, Comstock J C, Arumuganathan A K, Ming R . Genome size variation in threeSaccharum species. Euphytica, 2012,185:511-519.
doi: 10.1007/s10681-012-0664-6
[23] Iskandar H M, Simpson R S, Casu R E, Bonnett G D, Maclean D J, Manners J M . Comparison of reference genes for quantitative real-time polymerase chain reaction analysis of gene expression in sugarcane. Plant Mol Biol Rep, 2004,22:325-337.
doi: 10.1007/BF02772676
[24] Livak, K J, Schmittgen T D . Analysis of relative gene expression data using real-time quantitative PCR and the 2 -ΔΔCT method . Methods, 2001,25:402-408.
doi: 10.1006/meth.2001.1262 pmid: 11846609
[25] 夏会龙, 程文伟, 池小雅 . 镉胁迫对甘蔗生长及生理性状的影响. 中国土壤与肥料, 2009, ( 1):42-45.
Xia H L, Cheng W E, Chi X Y . Effects of Cd stress on the growth and physiological properties of sugarcane. Soil Fert Sci China, 2009, ( 1):42-45 (in Chinese with English abstract).
[26] 魏树和, 周启星, 王新 . 超积累植物龙葵及其对镉的富集特征. 环境科学, 2005,26(3):167-171.
Wei S F, Zhou Q X, Wang X . Cadmium-hyperaccumulator Solanum nigrum L. and its accumulating characteristics. Environ Sci, 2005,26(3):167-171 (in Chinese with English abstract).
[27] 姚诗音, 刘杰, 王怡璇, 朱园芳, 丰顺 . 青葙对镉的超富集特征及累积动态研究. 农业环境科学学报, 2017,36:1470-1476.
Yao S Y, Liu J, Wang Y X, Zhu Y F, Feng S . Cd hyperaccumulation and accumulative kinetics ofCelosia argentea Linn. for phytoremediation of Cd-contaminated soil. J Agro-Environt Sci, 2017,36:1470-1476 (in Chinese with English abstract).
[28] Guo W J, Meetam M, Goldsbrough P B . Examining the specific contributions of individualArabidopsis metallothioneins to copper distribution and metal tolerance. Plant Physiol, 2008,146:1697-1706.
doi: 10.1104/pp.108.115782 pmid: 18287486
[29] Guo W J Bundithya W, Goldsbrough P B . Characterization of theArabidopsis metallothionein gene family: tissue-specific expression and induction during senescence and in response to copper. New Phytol, 2003,159:369-381.
doi: 10.1046/j.1469-8137.2003.00813.x
[30] Zimeri A M, Dhankher O P, McCaig B, Meagher R B . The plant MT1 metallothioneins are stabilized by binding cadmiums and are required for cadmium tolerance and accumulation. Plant Mol Biol, 2005,58:839-855.
doi: 10.1007/s11103-005-8268-3
[31] Yang Z, Wu Y R, Li Y, Ling H Q, Chu C C . OsMT1a, a type 1 metallothionein, plays the pivotal role in zinc homeostasis and drought tolerance in rice. Plant Mol Biol, 2009,70:219-229.
doi: 10.1007/s11103-009-9466-1
[32] 姜廷波, 陈虹, 唐鑫华, 丁宝建, 王玉成, 李凤娟, 李绍臣 . 转金属硫蛋白基因(MT1)烟草抗Cd 2+胁迫的生理特性分析 . 作物学报, 2007,33:1902-1905.
Jiang T B, Chen H, Tang X H, Ding B J, Wang Y C, Li F J, Li S C . Analysis of physiologic characteristics for Cd 2+ tolerance on transgenic tobacco expressing metallothionein gene ( MT1). Acta Agron Sin, 2007,33:1902-1905 (in Chinese with English abstract).
[33] Grispen V M J, Hakvoort H W J, Bliek T, Verkleij J A C, Schat H . Combined expression of theArabidopsis metallothionein MT2b and the heavy metal transporting ATPase HMA4 enhances cadmium tolerance and the root to shoot translocation of cadmium and zinc in tobacco. Environ Exp Bot, 2011,72:71-76.
doi: 10.1016/j.envexpbot.2010.01.005
[34] 班巧英, 刘桂丰, 王玉成, 张大伟, 蒋丽丽 . 一个新的二色补血草金属硫蛋白基因LbMT2的克隆及其表达分析. 遗传, 2008,30:1075-1082.
doi: 10.3724/SP.J.1005.2008.01075
Ban Q Y, Liu G F, Wang Y C, Zhang D W, Jiang L L . Cloning and expression of a novel metallothionein gene LbMT2 from Limonium bicolor. Hereditas(Beijing), 2008,30:1075-1082 (in Chinese with English abstract).
doi: 10.3724/SP.J.1005.2008.01075
[35] Zhang J, Zhang M, Tian S, Lu L, Shohag M J I, Yang X . Metallothionein 2 (SaMT2) fromSedum alfrediihance confers increased Cd tolerance and acumulation in yeast and tobacco. PLoS One, 2014,9:e102750.
doi: 10.1371/journal.pone.0102750 pmid: 25032704
[36] Roosens N H, Bernard C, Leplae R, Verbruggen N . Evidence for copper homeostasis function of metallothionein (MT3) in the hyperaccumulator Thlaspi caerulescens. FEBS Lett, 2004,577:9-16.
doi: 10.1016/j.febslet.2004.08.084 pmid: 15527754
[37] Zhu G H, Zhang J J, Chen J S, Peng X X . Characterization of a rice metallothionein type 3 gene with different expression profiles under various nitrogen forms. Biol Planta, 2008,52:668-673.
doi: 10.1007/s10535-008-0129-x
[38] Hegelund J N, Schiller M, Kichey T, Hansen T H, Pedas P, Husted S, Schjoerring J K . Barley metallothioneins: MT3 and MT4 are localized in the grain aleurone layer and show differential Zinc binding. Plant Physiol, 2012,159:1125-1137.
doi: 10.1104/pp.112.197798
[1] LI Hui, LI De-Fang, DENG Yong, PAN Gen, CHEN An-Guo, ZHAO Li-Ning, TANG Hui-Juan. Expression analysis of abiotic stress response gene HcWRKY71 in kenaf and transformation of Arabidopsis [J]. Acta Agronomica Sinica, 2021, 47(6): 1090-1099.
[2] LYU Dong-Mei, ZHU Guang-Long, WANG Yue, SHI Yu, LU Fa-Guang, REN Zhen, LIU Yu-Qian, GU Li-Feng, LU Hai-Tong, Irshad Ahmad, JIAO Xiu-Rong, MENG Tian-Yao, ZHOU Gui-Sheng. Growth, physiological, and heavy metal accumulation traits at seedling stage under heavy metal stress in castor (Ricinus communis L.) [J]. Acta Agronomica Sinica, 2021, 47(4): 728-737.
[3] WEI Li-Juan, SHEN Shu-Lin, HUANG Xiao-Hu, MA Guo-Qiang, WANG Xi-Tong, YANG Yi-Ling, LI Huan-Dong, WANG Shu-Xian, ZHU Mei-Chen, TANG Zhang-Lin, LU Kun, LI Jia-Na, QU Cun-Min. Genome-wide association analysis reveals zinc-tolerant loci of rapeseed at germination stage [J]. Acta Agronomica Sinica, 2021, 47(2): 262-274.
[4] Yan-Ping XU, Ming YANG, Hong-Yan GUO, Qing-Hui YANG. Phytoremediation potential of five industrial hemp varieties on five heavy metal polluted soils [J]. Acta Agronomica Sinica, 2020, 46(12): 1970-1978.
[5] TANG Wen-Guang, XIAO Xiao-Ping, ZHANG Hai-Lin, HUANG Gui-Lin, TANG Hai-Ming, LI Chao, LIU Sheng-Li,WANG Ke. Effects of Rotational Tillage on Nutrient Storage Capacity and Cd Content in Tilth Soil of Double-cropping Rice Region [J]. Acta Agron Sin, 2018, 44(01): 105-114.
[6] YUAN Lian-Yu,CHEN Ying-Juan,WEI Xu,TONG Hua-Rong*. Cloning and Function Analysis of Metal Tolerance Gene (CsMTP11) in Tea Plant (Camellia sinensis L. O. Kuntze) [J]. Acta Agron Sin, 2017, 43(05): 708-717.
[7] WANG Wei,SONG Wen,YIN Shuang-Yi,XU Chen-Wu. Discussion of Multistage Sampling Optimum Test Plans on Rice Cadmium Detection for Jiangsu Province [J]. Acta Agron Sin, 2014, 40(11): 2052-2056.
[8] TANG Wen-Guang, TANG Hai-Ming, LUO Zun-Chang, HONG Ke, YANG Guang-Li, XIAO Xiao-Peng. Impacts of Winter Planting Patterns on Soil Heavy Metal Content and Grain Quality in Late Rice in Double Cropping Rice Area [J]. Acta Agron Sin, 2011, 37(08): 1457-1464.
[9] XIANG Yan-Ci,GUAN Chun-Yun,HUANG Huang,YAN Ming-Li,PENG Xiu-Hua. Effects of Phosphorus on Growth and Uptake of Heavy Metals in Plants Grown in the Soil Contaminated by uranium Tailing [J]. Acta Agron Sin, 2010, 36(1): 154-162.
[10] JIANG Ting-Bo;CHEN Hong;TANG Xin-Huan;DING Bao-Jian;WANG Yu-Cheng;LI Feng-Juan;LI Shao-Chen. Analysis of Physiologic Characteristics for Cd2+ Tolerance on Transgenic Tobacco Expressing Metallothionein Gene (MT1) [J]. Acta Agron Sin, 2007, 33(11): 1902-1905.
[11] CHENG Wang-Da; ZHANG Guo-Ping; YAO Hai-Gen; WU Wei; TANG Mei-Ling; ZHU Zhu-Jun and XU Ming. Genotypic and Environmental Variation and their Stability of As, Cr, Cd, Ni and Pb Concentrations in the Grains of Japonica Rice [J]. Acta Agron Sin, 2006, 32(04): 573-579.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!