Bao Y, Liu GF, Shi XP, X W, Ning GG, Liu J, Bao MZ (2012) Primary and repetitive secondary somatic embryogenesis in Rosa hybrida ‘Samantha’. Plant Cell Tiss Org Cult 109:411–418. https://doi.org/10.1007/s11240-011-0105-6
Bellieny-Rabelo D, De Oliveira EA, Ribeiro ES, Costa EP, Oliveira AE, Venancio TM (2016) Transcriptome analysis uncovers key regulatory and metabolic aspects of soybean embryonic axes during germination. Sci Rep 6:36009. https://doi.org/10.1038/srep36009
Article CAS PubMed PubMed Central Google Scholar
Bogdanović MD, Ćuković KB, Subotić AR, Dragićević MB, Simonović AD, Filipović BK, Todorović SI (2021) Secondary somatic embryogenesis in Centaurium erythraea Rafn. Plants 10. https://doi.org/10.3390/plants10020199
Cai Y, Li S, Jiao G, Sheng Z, Wu Y, Shao G, Xie L, Peng C, Xu J, Tang S, Wei X, Hu P (2018) OsPK2 encodes a plastidic pyruvate kinase involved in rice endosperm starch synthesis, compound granule formation and grain filling. Plant Biotechnol J 16:1878–1891. https://doi.org/10.1111/pbi.12923
Article CAS PubMed PubMed Central Google Scholar
Ding CY, Kang XL, Hu XX, Wu R, Yuan MJ, Weng SD, Du L (2024) Study on physiological and biochemical characteristics being used for identification of different plantlet regeneration approaches from somatic embryo of Rosa hybrida ‘J. F. Kennedy.’ Plant Cell Tissue Organ Cult 159:1–12. https://doi.org/10.1007/s11240-024-02912-4
Du L, Kang XL, Guo HR, Zhu ZF, Wu R, Yuan MJ, Ding CY (2024) Cotyledonary somatic embryo is one kind of intermediate material similar to callus in the process of in vitro tissue culture from Rosa hybrida ‘John F. Kennedy’ BMC Genomics 25:362. https://doi.org/10.1186/s12864-024-10256-8
Article CAS PubMed Google Scholar
Fehér A (2019) Callus, dedifferentiation, totipotency, somatic embryogenesis: what these terms mean in the era of molecular plant biology? Front Plant Sci 10:536. https://doi.org/10.3389/fpls.2019.00536
Article PubMed PubMed Central Google Scholar
Flügge UI, Häusler RE, Ludewig F, Gierth M (2011) The role of transporters in supplying energy to plant plastids. J Exp Bot 62:2381–2392. https://doi.org/10.1093/JXB/ERQ361
Gupta A, Singh M, Laxmi A (2015) Interaction between glucose and brassinosteroid during the regulation of lateral root development in Arabidopsis. Plant Physiol 168:307–320. https://doi.org/10.1104/pp.114.256313
Article CAS PubMed PubMed Central Google Scholar
He D, Zhang M, He S, Hua C, Guo HN, Chang YH, Liu Y, Wang Z, Liu YP (2024) Transcriptome analysis reveals the role of sucrose and starch metabolism and systemic homeostasis in seed abortion in distant hybrids of Peony. J Plant Growth Regul 43:3776–3794. https://doi.org/10.1007/s00344-024-11334-7
Hou J, Zhang H, Liu J, Reid S, Liu T, Xu S, Tian Z, Sonnewald U, Song B, Xie C (2017) Amylases StAmy23, StBAM1 and StBAM9 regulate cold-induced sweetening of potato tubers in distinct ways. J Exp Bot 68:2317–2331. https://doi.org/10.1093/jxb/erx076
Article CAS PubMed PubMed Central Google Scholar
Kang XL (2024) Identification of different plantlet regeneration approaches from somatic embryo of Rosa hybrida L. and study on its related mechanisms. [M. D. Dissertation]. Nanyang: Nanyang Normal University. (in Chinese)
Kim HB, Cho JI, Ryoo N, Shin DH, Park YI, Hwang YS, Lee SK, An G, Jeon JS (2016) Role of rice cytosolic hexokinase OsHXK7 in sugar signaling and metabolism. J Integr Plant Biol 58:127–135. https://doi.org/10.1111/jipb.12366
Article CAS PubMed Google Scholar
Liu YM, Qu JT, Zhang L, Xu XY, Wei G, Zhou ZF, Ren MZ, Cao MJ (2019) Identification and characterization of the TCA cycle genes in maize. BMC Plant Biol 19(1):592. https://doi.org/10.1186/s12870-019-2213-0
Article CAS PubMed PubMed Central Google Scholar
Lu Y, Sharkey TD (2006) The importance of maltose in transitory starch breakdown. Plant Cell Environ 29:353–366. https://doi.org/10.1111/j.1365-3040.2005.01480.x
Article CAS PubMed Google Scholar
Mazri MA, Naciri R, Belkoura I (2020) Maturation and conversion of somatic embryos derived from seeds of Olive ( Olea europaea L.) cv. Dahbia: occurrence of secondary embryogenesis and adventitious bud formation. Plants 9:1489. https://doi.org/10.3390/plants9111489
Article CAS PubMed PubMed Central Google Scholar
Megguer CA, Fugate KK, Lafta AM, Ferrareze JP, Deckard EL, Campbell LG, Lulai EC, Finger FL (2017) Glycolysis is dynamic and relates closely to respiration rate in stored sugar beet roots. Front Plant Sci 8:861. https://doi.org/10.3389/fpls.2017.00861
Article PubMed PubMed Central Google Scholar
Monroe JD, Storm AR (2018) The Arabidopsis β-amylase (BAM) gene family: diversity of form and function. Plant Sci 276:163–170. https://doi.org/10.1016/j.plantsci.2018.08.016.
Article CAS PubMed Google Scholar
Murashige T, Skoog F (1962) A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiol Plant 15:473–497. https://doi.org/10.1111/j.1399-3054.1962.tb08052.x
Pujadas G, Palau J (2021) Evolution of alpha-amylases: architectural features and key residues in the stabilization of the (beta/alpha) (8) scaffold. Mol Biol Evol 18:38–54. https://doi.org/10.1093/oxfordjournals.molbev.a003718
Raza G, Singh MB, Bhalla PL (2020) Somatic embryogenesis and plant regeneration from commercial soybean cultivars. Plants 9:38. https://doi.org/10.3390/plants9010038
Reinhold H, Soyk S, Simková K, Hostettler C, Marafino J, Mainiero S, Vaughan CK, Monroe JD, Zeeman SC (2011) Β-amylaselike proteins function as transcription factors in Arabidopsis, controlling shoot growth and development. Plant Cell 23:1391–1403. https://doi.org/10.1105/tpc.110.081950
Article CAS PubMed PubMed Central Google Scholar
Roschzttardtz H, Fuentes I, Vásquez M, Corvalán C, León G, Gómez I, Araya A, Holuigue L, Vicente-Carbajosa J, Jordana X (2009) A nuclear gene encoding the iron-sulfur subunit of mitochondrial complex II is regulated by B3 domain transcription factors during seed development in Arabidopsis. Plant Physiol 150:84–95. https://doi.org/10.1104/pp.109.136531
Article CAS PubMed PubMed Central Google Scholar
Srivastava G, Kayastha AM (2014) Β-amylase from starchless seeds of Trigonella foenum-graecum and its localization in germinating seeds. PLoS One 9:e88697. https://doi.org/10.1371/journal.pone.0088697
Article CAS PubMed PubMed Central Google Scholar
Smith AM, Zeeman SC, Smith SM (2005) Starch degradation. Ann Rev. Plant Biol 56:73–98. https://doi.org/10.1007/978-4-431-55495-0_7
Sun S, Hu C, Qi X, Chen J, Zhong Y, Muhammad A, Lin M, Fang J (2021) The AaCBF4-AaBAM3.1 module enhances freezing tolerance of kiwi fruit (Actinidia arguta). Hortic Res 8:97. https://doi.org/10.1038/s41438-021-00530-1
Article CAS PubMed PubMed Central Google Scholar
Tran PT, Citovsky V (2021) Receptor-like kinase BAM1 facilitates early movement of the tobacco mosaic virus. Commun Biol 4:1–11. https://doi.org/10.1038/s42003-021-02041-0
van der Merwe MJ, Osorio S, Moritz T, Nunes-Nesi A, Fernie AR (2009) Decreased mitochondrial activities of malate dehydrogenase and fumarase in tomato lead to altered root growth and architecture via diverse mechanisms. Plant Physiol 149:653–669. https://doi.org/10.1104/pp.108.130518
Article CAS PubMed PubMed Central Google Scholar
Wang H, Zhao P, Shen X, Xia ZQ, Zhou XC, Chen X, Lu C, Wang WQ (2021) Genome-wide survey of the phosphofructokinase family in cassava and functional characterization in response to oxygen-deficient stress. BMC Plant Biol 21:376. https://doi.org/10.1186/s12870-021-03139-7
Article CAS PubMed PubMed Central Google Scholar
Wang LN, Cui DH, Zhao XY, He M (2017) The important role of the citric acid cycle in plants. Genom Appl Biol 8:25–29.
Comments (0)