[1] 谢华安, 张建福, 王乌齐, 郑家团, 黄庭旭. 超级稻育种实践和前景. 分子植物育种, 2006, 4(S3): 4-10.
Xie H A, Zhang J F, Wang W Q, Zheng J T, Huang T X. Practice and prospect on breeding of super-hybridization rice in China. Mol Plant Breed, 2006, 4(3S): 4-10. (in Chinese with English abstract)
[2] 武小金, 尹华奇. 杂交水稻品质改良的遗传基础和途径. 杂交水稻, 1994(2): 5-8.
Wu X J, Yin H Q. Genetic basis of and approach to grain quality improvement in hybrid rice. Hybrid Rice, 1994(2): 5-8. (in Chinese with English abstract)
[3] 卢毅, 路兴花, 张青峰, 余建国, 肖雄雄, 庞林江, 成纪予. 稻米直链淀粉与米饭物性及食味品质的关联特征研究. 食品科技, 2018, 43(10): 219-223.
Lu Y, Lu X H, Zhang Q F, Yu J G, Xiao X X, Pang L J, Cheng J Y. Correlation of rice amylose with physical properties and taste quality of rice. Food Sci Technol, 2018, 43(10): 219-223. (in Chinese with English abstract)
[4] Seferoglu A B, Koper K, Can F B, Cevahir G, Kavalir I H. Enhanced heterotetrameric assembly of potato ADP-Glucose pyrophosphorylase using reverse genetics. Plant Cell Physiol, 2014, 55(8): 1473-1483.
[5] Dian W, Jiang H, Chen Q, Liu F, Wu P. Cloning and characterization of the granule-bound starch synthase II gene in rice: gene expression is regulated by the nitrogen level, sugar and circadian rhythm. Planta, 2003, 218(2): 261-268.
[6] 陈雅玲, 包劲松. 水稻胚乳淀粉合成相关酶的结构、功能及其互作研究进展. 中国水稻科学, 2017, 31(1): 1-12.
Chen Y L, Bao J S. Progress in structures, function and interactions of starch synthesis related enzymes in rice endosperm. Chin J Rice Sci, 2017, 31(1): 1-12. (in Chinese with English abstract)
[7] 潘鹏屹, 朱建平, 王云龙, 郝媛媛, 蔡跃, 张文伟, 江玲, 王益华, 万建民. 水稻粉质胚乳突变体ws的表型分析及基因克隆. 中国水稻科学, 2016, 30(5): 447-457.
Pan P Y, Zhu J P, Wang Y L, Hao Y Y, Cai Y, Zhang W W, Wang Y H, Wan J M. Phenotyping and gene cloning of a floury endosperm mutant ws in rice. Chin J Rice Sci, 2016, 30(5): 447-457. (in Chinese with English abstract)
[8] 方鹏飞, 李三峰, 焦桂爱, 谢黎红, 胡培松, 魏祥进, 唐绍清. 水稻粉质胚乳突变体flo7的理化性质及基因定位. 中国水稻科学, 2014, 28(5): 447-457.
Fang P F, Li S F, Jiao G A, Xie L H, Hu P S, Wei X J, Tang S Q. Physicochemical property analysis and gene mapping of a floury endosperm mutant flo7 in rice. Chin J Rice Sci, 2014, 28(5): 447-457. (in Chinese with English abstract)
[9] Kaushik R P, Khush G S. Genetic analysis of endosperm mutants in rice (Oryza sativa L.). Theor Appl Genet, 1991, 83(2): 146-152.
[10] She K, Kusano H, Koizumi K, Yamakawa H, Hakata M, Imamura T, Fukuda M, Naito N, Tsurumaki Y, Yaeshima M, Tsuge T, Matsumoto K, Kudoh M, Itoh E, Kikuchi S, Kishimoto N, Yazaki J, Ando T, Yano M, Aoyama T, Sasaki T, Satoh H, Shimada H. A novel factor FLOURY ENDOSPERM2 is involved in regulation of rice grain size and starch quality. Plant Cell, 2010, 22(10): 3280-3294.
[11] Kang H, Park S, Matsuoka M, An G. White-core endosperm floury endosperm4 in rice is generated by knockout mutations in the C4-type pyruvate orthophosphate dikinase gene (OsPPDKB). Plant J, 2005, 42(6): 901-911.
[12] Peng C, Wang Y, Liu F, Ren Y, Zhou K N, Lü J, Zheng M, Zhao S L, Zhang L, Wang C M, Jiang L, Zhang X, Guo X P, Bao Y Q, Wan J M. FLOURY ENDOSPERM6 encodes a CBM48 domain-containing protein involved in compound granule formation and starch synthesis in rice endosperm. Plant J, 2014, 77(6): 917-930.
[13] Zhang L, Ren Y, Lu B, Yang C Y, Feng Z M, Liu Z, Chen J, Ma W W, Wang Y, Yu X W, Wang Y L, Zhang W W, Wang Y H, Liu S J, Wu F Q, Zhang X, Guo X P, Bao Y Q, Jiang L, Wan J M. FLOURY ENDOSPERM7 encodes a regulator of starch synthesis and amyloplast development essential for peripheral endosperm development in rice. J Exp Bot, 2016, 67(3): 633-647.
[14] Wu M M, Ren Y L, Cai M H, Wang Y L, Zhu S S, Zhu J P, Hao Y Y, Teng X, Zhu X P, Jing R N, Zhang H, Zhong M S, Wang Y F, Lei C L, Zhang X, Guo X P, Cheng Z J, Lin Q B, Wang J, Jiang L, Bao Y Q, Wang Y H, Wan J M. Rice FLOURY ENDOSPERM10 encodes a pentatricopeptide repeat protein that is essential for the trans-splicing of mitochondrial nad1 intron 1 and endosperm development. New Phytol, 2019, 233: 736-750.
[15] Teng X, Zhong M S, Zhu X P, Wang C M, Ren Y L, Wang Y L, Zhang H, Jiang L, Wang D, Hao Y Y, Wu M M, Zhu J P, Zhang X, Guo X P, Wang Y H, Wan J M. FLOURY ENDOSPERM16 encoding a NAD-dependent cytosolic malate dehydrogenase plays an important role in starch synthesis and seed development in rice. Plant Biotechnol J, 2019, 17: 1914-1927.
[16] Long W, Wang Y, Zhu S, Jing W, Wang Y H, Ren Y L, Tian Y L, Liu S J, Liu X, Chen L M, Wang D, Zhong M S, Zhang Y Y, Hu T T, Zhu J P, Hao Y Y, Zhu X P, Zhang W W, Wang C M, Zhang W H, Wan J M. FLOURY SHRUNKEN ENDOSPERM1 connects phospholipid metabolism and amyloplast development in rice. Plant Physiol, 2018, 177(2): 698-712.
[17] 李景芳, 田云录, 刘喜, 刘世家, 陈亮明, 江玲, 张文伟, 徐大勇, 王益华, 万建民. 鸟苷酸激酶OsGK1对水稻种子发育至关重要. 中国水稻科学, 2018, 32(5): 415-426.
Li J F, Tian Y L, Liu X, Liu S J, Chen L M, Jiang L, Zhang W W, Xu D Y, Wang Y H, Wan J M. The guanylate kinase OsGK1 is essential for seed development in rice. Chin J Rice Sci, 2018, 32(5): 415-426. (in Chinese with English abstract)
[18] 于艳芳, 刘喜, 田云录, 刘世家, 王云龙, 张文伟, 江玲, 王益华, 万建民. 水稻粉质胚乳fse3突变体的表型分析及基因定位. 中国农业科学, 2018, 51(11): 2023-2037.
Yu Y F, Liu X, Tian Y L, Liu S J, Wang Y L, Zhang W W, Jiang L, Wang Y H, Wan J M. Phenotypic analysis and gene mapping of a floury and shrunken endosperm mutant fse3 in rice. Sci Agric Sin, 2018, 51(11): 2023-2037. (in Chinese with English abstract)
[19] Zhang C S, Lu Q, Verma D P S. Removal of feedback inhibition of Δ1-pyrroline-5-carboxylate synthetase, a bifunctional enzyme catalyzing the first two steps of proline biosynthesis in plants. J Biol Chem, 1995, 270(35): 20491-20496.
[20] Lehmann S, Funck D, Szabados L, Rentsch D. Proline metabolism and transport in plant development. Amino Acids, 2010, 39(4): 949-962.
[21] Hu C, Delauney A J, Verma D. Bifunctional enzyme (Delta-1-pyrroline-5-carboxylate synthetase) catalyzes the 1st 2 steps in proline biosynthesis in plants. Proc Natl Acad Sci USA, 1992, 89(19): 9354-9358.
[22] Kim G, Nam Y. A novel Δ1-pyrroline-5-carboxylate synthetase gene of medicago truncatula plays a predominant role in stress-induced proline accumulation during symbiotic nitrogen fixation. J Plant Physiol, 2013, 170(3): 291-302.
[23] Zang D, Wang C, Ji X, Wang Y C. Tamarix hispida zinc finger protein ThZFP1 participates in salt and osmotic stress tolerance by increasing proline content and SOD and POD activities. Plant Sci, 2015, 235: 111-121.
[24] Su M, Li X, Ma X, Peng X J, Zhao A G, Cheng L Q, Chen S Y, Liu G S. Cloning two P5CS genes from bioenergy sorghum and their expression profiles under abiotic stresses and MeJA treatmen. Plant Sci, 2011, 181(6SI): 652-659.
[25] Chu H M, Nguyen T T H, Chu H L, Le V S, Chu H H. Characteristics of the gene encoding pyrroline-5- carboxylate synthase (P5CS) in Vietnamese soybean cultivars (Glycine max L. Merrill)// Proceedings of International Conference on Biology, Environment and Chemistry, 2011: 319-323.
[26] Chen J B, Yang J W, Zhang Z Y, Feng X F, Wang S M. Two P5CS genes from common bean exhibiting different tolerance to salt stress in transgenic Arabidopsis. J Genet, 2013, 92(3): 461-469.
[27] Kim D, Shibato J, Agrawl G K, Fujihara S, Iwahashi H, Kim du H, Shim IeS, Rakwal R. Gene transcription in the leaves of rice undergoing salt-induced morphological changes (Oryza sativa L.). Mol&Cells, 2007, 24(1): 45-59.
[28] Wan P, Fu K, Lu F, Guo W C, Li G Q. A putative Δ1-pyrroline-5-carboxylate synthetase involved in the biosynthesis of proline and arginine in Leptinotarsa decemlineata. J Insect Physiol, 2014, 71: 105-113.
[29] Bicknell L S, Pitt J, Aftimos S, Ramadas R, Maw M A, Robertso S P. A missense mutation in ALDH18A1, encoding Delta 1-pyrroline-5-carboxylate synthase (P5CS), causes an autosomal recessive neurocutaneous syndrome. Eur J Human Genet, 2008, 16(10): 1176-1186.
[30] 易健明, 屈武斌, 张成岗. 实时荧光定量PCR的数据分析方法. 生物技术通讯, 2015, 26(1): 140-145.
Yi J M, Qu W B, Zhang C G. Date analysis methods of real-time fluorescent quantitative PCR. Lett Biotechnol, 2015, 26(1): 140-145. (in Chinese with English abstract)
[31] Wang Y, Wang C, Zheng M, Lyu J, Xu Y, Li X H, Niu M, Long W H, Wang D, Wang H Y, Terzaghi W, Wang Y H, Wan J M. WHITE PANICLE1, a Val-tRNA synthetase regulating chloroplast ribosome biogenesis in rice, is essential for early chloroplast development. Plant Physiol, 2016, 170(4): 2110-2123.
[32] Hong Z L, Karuna L, Zhang Z M, Verma D. Removal of feedback inhibition of 1-pyrroline-5-carboxylate synthetase results in increased proline. Plant Physiol, 2000, 122(4): 1129-1136.
[33] Székely G, ábrahám E, Csépl? A, Rigó G, Zsigmond L, Csiszár J, Ayaydin F, Strizhov N, Jásik J, Schmelzer E, Koncz C, Szabados L. Duplicated P5CS genes of Arabidopsis play distinct roles in stress regulation and developmental control of proline biosynthesis. Plant J, 2008, 53(1): 11-28.
[34] Deauney A J, Verma D. Proline biosynthesis and osmoregulation in plants. Plant J, 1993 4(2): 215-223.
[35] Siripornadulsil S, Traina S, Verma D, Richard T. Sayre molecular mechanisms of proline-mediated tolerance to toxic heavy metals in transgenic microalgae. Plant Cell, 2002, 14(11): 2837-2847.
[36] Makryaleas K, Drauz K, Bommarius A. Method for the preparation of D-arginine and L-ornithine. US Patent, 1997(5): 591-613.
[37] Kurhajec A. Orgithine aynthesis. US Patent, 1961(3): 168-588.
[38] Ehsanpour A A, Fatahian N. Effects of salt and proline on Medicago sativa callus. Plant Cell Tissue Organ Cult, 2003, 73(1): 53-56.
[39] Trovato M, Mattioli R, Costantino P. Multiple roles of proline in plant stress tolerance and development. Rend Linct, 2008, 19(4): 325-346.
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