| [1] |
Liu C. 2009. Physiology mechanism and differential protein of fraxinus mandshurica somatic embrygenesis acompanied explant browning. Thesis. Northeast Forestry University, China. pp. 21−23 |
| [2] |
Wang J, Dong J, Liu W, Cao F, Wang G, et al. 2019. Research on growth, browning and flavonoid accumulation of
Ginkgo biloba callus.
|
| [3] |
Hao Z, Shi J, Wu H, Yan Y, Xing K, et al. 2023. Phytosulfokine contributes to suspension culture of
Cunninghamia lanceolata through its impact on redox homeostasis.
|
| [4] |
Zhang D, Wang R, Xiao J, Zhu S, Li X, et al. 2022. An integrated physiology, cytology, and proteomics analysis reveals a network of sugarcane protoplast responses to enzymolysis.
|
| [5] |
Liu J, Zhang X, Poudyal BK, Zhang Y, Dong Z, et al. 2008. Studies on factors affecting browning of pear explants in vitro and anti-browning measures. Journal of Fruit Science 25:727−31 |
| [6] |
Duan Y, Guo W. 2009. Study on callus browning in relation to polyphenol content and polyphenol oxidase activity among various citrus embryogenic calli. Chinese Agricultural Science Bulletin 25:117−20 |
| [7] |
Li F, Li Z, Gao Z, Wang G, Li H, et al. 2023. A laccase gene (
LcLac) was involved in polyphenol metabolism and tissue browning of litchi callus.
|
| [8] |
Li JF, Deng Z, Dong H, Tsao R, Liu X. 2023. Substrate specificity of polyphenol oxidase and its selectivity towards polyphenols: unlocking the browning mechanism of fresh lotus root (
Nelumbo nucifera Gaertn.).
|
| [9] |
Mahmoud LM, Killiny N, Dutt M. 2024. Melatonin supplementation enhances browning suppression and improves transformation efficiency and regeneration of transgenic rough lemon plants (
Citrus ×
jambhiri).
|
| [10] |
Xu X, Zhu D, Huan Z, Geng X, Ran J. 2023. Mechanisms of tissue culture browning in five Magnoliaceae family species.
|
| [11] |
Kim C, Dai W. 2020. Plant regeneration of red raspberry (
Rubus idaeus) cultivars 'Joan J' and 'Polana'.
|
| [12] |
Wang J, Fang SZ. 2023. Effects of different anti-browning agents on enzyme activity and growth in callus of
Cyclocarya paliurus.
|
| [13] |
Li X, Wang C, Zhu J, He Q, Liu F. 2019. Effect of drying rate on cytochemical localization of phenolic substance and polyphenol oxidase and browning in thompson seedless grape.
|
| [14] |
Bonga JM. 1987. Tree tissue culture applications.
|
| [15] |
Cai X, Wei H, Liu C, Ren XX, Thi LT, et al. 2020. Synergistic effect of NaCl pretreatment and PVP on browning suppression and callus induction from petal explants of
Paeonia Lactiflora Pall. 'Festival Maxima'.
|
| [16] |
Taghizadeh M, Dastjerdi MG. 2021. Inhibition of browning problem during the callogenesis of
Spartium junceum L.
|
| [17] |
Tarinejad A. 2013. Effects of disinfectants and antibiotics on contamination during propagation of walnut ( Juglans regia L.). Research on Crops 14:219−25 |
| [18] |
Fang H, Dong Y, Zhou R, Wang Q, Duan Q, et al. 2022. Optimization of the induction, germination, and plant regeneration system for somatic embryos in apomictic walnut (
Juglans regia L.).
|
| [19] |
Wojtania A, Skrzypek E, Gabryszewska E. 2015. Effect of cytokinin, sucrose and nitrogen salts concentrations on the growth and development and phenolics content in Magnolia × soulangiana 'Coates' shoots in vitro. Acta Scientiarum Polonorum Hortorum Cultus 14:51−62 |
| [20] |
Han M, Gleave AP, Wang T. 2010. Efficient transformation of
Actinidia arguta by reducing the strength of basal salts in the medium to alleviate callus browning.
|
| [21] |
Panghal S, Soni SS. 2014. In vitro studies on effect of different concentration of NaCl on Jatropha curcas. Journal of Environmental Biology 35:709−12 |
| [22] |
Gou W, Zheng P, Wang K, Zhang L, Akram NA. 2016. Salinity-induced callus browning and re-differentiation, root formation by plantlets and anatomical structures of plantlet leaves in two Malus species. Pakistan Journal of Botany 48:1393−98 |
| [23] |
Lai S, Wu Z, Chen J, Ying Y. 2023. Mechanism and regulation of explants browning in tissue culture of
Cyclobalanopsis chungii.
|
| [24] |
Li S, Lin L, Jiang T, Zhu J, Liu B. 2023. Callus induction and culture conditions optimization of moso bamboo (
Phyllostachys edulis).
|
| [25] |
Feng J, Zhu C, Cao J, Liu C, Zhang J, et al. 2023. Genome-wide identification and expression analysis of the
NRT genes in
Ginkgo biloba under nitrate treatment reveal the potential roles during calluses browning.
|
| [26] |
Swarnkar PL, Bohra SP, Chandra N. 1986. Biochemical changes during growth and differentiation of the callus of
Solanum surattense.
|
| [27] |
Gibson SI. 2000. Plant sugar-response pathways. Part of a complex regulatory web.
|
| [28] |
Jan R, Khan MA, Asaf S, Lee IJ, Kim KM. 2020. Modulation of sugar and nitrogen in callus induction media alter PAL pathway, SA and biomass accumulation in rice callus.
|
| [29] |
Solfanelli C, Poggi A, Loreti E, Alpi A, Perata P. 2006. Sucrose-specific induction of the anthocyanin biosynthetic pathway in
Arabidopsis.
|
| [30] |
Kim SS, Guo DD, Jung DC, Kwon ST. 2003. Multiple shoots regeneration and in vitro bulblet formation from garlic callus. Journal of Plant Biotechnology 5:95−99 |
| [31] |
Rahman Z, Ramli A, Kamaruzaman R, Seman Z, Othman A, et al. 2015. Efficient plant regeneration of malaysian aromatic rice ( Oryza sativa L.) via improved somatic embryogenesis pathway. Emirates Journal of Food and Agriculture 27:857−63 |
| [32] |
Yari Khosroushahi A, Naderi-Manesh H, Toft Simonsen H. 2011. Effect of antioxidants and carbohydrates in callus cultures of
Taxus brevifolia: evaluation of browning, callus growth, total phenolics and paclitaxel production.
|
| [33] |
Du Y, Li Y, Ma Y, Yang X. 2007. Factors affecting explant browning in tissue culture of Hippophae rhamnoides L. Journal of Agricultural University of Hebei 30:40−43 |
| [34] |
Harahap F, Diningrat DS, Poerwanto R, Nasution NEA, Hasibuan RFM. 2019.
In vitro callus induction of Sipahutar pineapple (
Ananas comosus L.) from north Sumatra Indonesia.
|
| [35] |
Ma NL, Khoo SC, Lee JX, Soon CF, Shukor NAB. 2020. Efficient micropropagation of
Dendrobium aurantiacum from shoot explant.
|
| [36] |
Zhang D, Wang Y, Shi P, Jin L, Zhao Z, et al. 2019. Different exogenous hormones in the process of callus induction: effects on the browning rate of oil palm leaf. Chinese Agricultural Science Bulletin 35:47−51 |
| [37] |
Wang J, Gao J, Fan W, Dong J, Tang F, et al. 2023. Construction of tissue culture system of
Onobrychis viciaefolia Scop 'Mengnong' anthers.
|
| [38] |
Lu Z, Xia Z. 1991. Study on tissue and protoplast culture of wild cotton ( Gossypium davidsonii). Acta Botanica Sinica 33:98−103,172 |
| [39] |
Shirazi MR, Rahpeyma SA, Zolala J. 2020. A new approach to prevent hazelnut callus browning by modification of sub-culture.
|
| [40] |
Gao J, Zhang P, Xue J, Xue Y, Wang S, et al. 2019. Advances in phenolic substances and their effects on browning in woody plant tissue culture.
|
| [41] |
Wang Y, Dai X. 2023. Effect of different light treatments on callus formation and browning of
Stellaria dichotoma.
|
| [42] |
Yu N. 2020. Optimization on anti-browning culture conditions of young stem tip explants in tissue culture of
Ginkgo biloba.
|
| [43] |
Chen Y, Lin H, Li Y, Lin M, Chen J. 2019. Non-enzymatic browning and the kinetic model of 5-hydroxymethylfurfural formation in residual solution of vinegar soaked-soybean.
|
| [44] |
Embs RJ, Markakis P. 1965. The mechanism of sulfite inhibition of browning caused by polyphenol oxidase.
|
| [45] |
Sae-leaw T, Benjakul S, Simpson BK. 2017. Effect of catechin and its derivatives on inhibition of polyphenoloxidase and melanosis of Pacific white shrimp.
|
| [46] |
Ahmad I, Jaskani MJ, Nafees M, Ashraf I, Qureshi R. 2016. Control of media browning in micropropagation of guava ( Psidium guajava L.). Pakistan Journal of Botany 48:713−16 |
| [47] |
Chi M, Bhagwat B, Lane W, Tang G, Su Y, et al. 2014. Reduced polyphenol oxidase gene expression and enzymatic browning in potato (
Solanum tuberosum L.) with artificial microRNAs.
|
| [48] |
Pretzler M, Rompel A. 2018. What causes the different functionality in type-III-copper enzymes? A state of the art perspective. Inorganica Chimica Acta 481:25−31 |
| [49] |
Laukkanen H, Rautiainen L, Taulavuori E, Hohtola A. 2000. Changes in cellular structures and enzymatic activities during browning of Scots pine callus derived from mature buds.
|
| [50] |
Tang W, Newton RJ. 2004. Increase of polyphenol oxidase and decrease of polyamines correlate with tissue browning in Virginia pine (
Pinus virginiana Mill.).
|
| [51] |
Zhao S, Wang H, Liu K, Li L, Yang J, et al. 2021. The role of
JrPPOs in the browning of walnut explants.
|
| [52] |
Mittler R. 2017. ROS are good.
|
| [53] |
Hesami M, Tohidfar M, Alizadeh M, Daneshvar MH. 2020. Effects of sodium nitroprusside on callus browning of
Ficus religiosa: an important medicinal plant.
|
| [54] |
Tomás-Barberán FA, Espín JC. 2001. Phenolic compounds and related enzymes as determinants of quality in fruits and vegetables.
|
| [55] |
Pang B, Feng X, Huang J, Zhou Y, Huang Z. 2019. Effects of PBU and 6-BA on POD genes and enzyme activity in
Eucalyptus urophyllus callus.
|
| [56] |
Xie J, Qi B, Mou C, Wang L, Jiao Y, et al. 2022.
BREVIPEDICELLUS and
ERECTA control the expression of
AtPRX17 to prevent
Arabidopsis callus browning.
|
| [57] |
Wang X, Zhang X, Jia P, Luan H, Qi G, et al. 2023. Transcriptomics and metabolomics provide insight into the anti-browning mechanism of selenium in freshly cut apples.
|
| [58] |
Wang H, Zhang S, Fu Q, Wang Z, Liu X, et al. 2023. Transcriptomic and metabolomic analysis reveals a protein module involved in preharvest apple peel browning.
|
| [59] |
Wang P, Zhang L, Zhao L, Zhang X, Zhang H, et al. 2020. Comprehensive analysis of metabolic fluxes from leucoanthocyanins to anthocyanins and proanthocyanidins (PAs).
|
| [60] |
Yang X, Xu Q, Le L, Zhou T, Yu W, et al. 2023. Comparative histology, transcriptome, and metabolite profiling unravel the browning mechanisms of calli derived from ginkgo (
Ginkgo biloba L.).
|
| [61] |
Liao L, Vimolmangkang S, Wei G, Zhou H, Korban SS, et al. 2015. Molecular characterization of genes encoding leucoanthocyanidin reductase involved in proanthocyanidin biosynthesis in apple.
|
| [62] |
Sun HJ, Luo ML, Zhou X, Zhou Q, Sun YY, et al. 2020. PuMYB21/PuMYB54 coordinate to activate
PuPLDβ1 transcription during peel browning of cold-stored ‘Nanguo’ pears.
|
| [63] |
Sun Y, Luo M, Ge W, Zhou X, Zhou Q, et al. 2022. Phenylpropanoid metabolism in relation to peel browning development of cold-stored 'Nanguo' pears.
|
| [64] |
Yang C, Sun N, Qin X, Liu Y, Sui M, et al. 2024. Multi-omics analysis reveals the biosynthesis of flavonoids during the browning process of
Malus sieversii explants.
|
| [65] |
Ackah S, Xue S, Osei R, Kweku-Amagloh F, Zong Y, et al. 2022. Chitosan treatment promotes wound healing of apple by eliciting phenylpropanoid pathway and enzymatic browning of wounds.
|
| [66] |
Persic M, Mikulic-Petkovsek M, Halbwirth H, Solar A, Veberic R, et al. 2018. Red walnut: characterization of the phenolic profiles, activities and gene expression of selected enzymes related to the phenylpropanoid pathway in pellicle during walnut development.
|
| [67] |
Fraser CM, Chapple C. 2011. The phenylpropanoid pathway in
Arabidopsis.
|
| [68] |
Shi R, Shuford CM, Wang JP, Sun YH, Yang Z, et al. 2013. Regulation of phenylalanine ammonia-lyase (PAL) gene family in wood forming tissue of
Populus trichocarpa.
|
| [69] |
Dong YS, Fu CH, Su P, Xu XP, Yuan J, et al. 2016. Mechanisms and effective control of physiological browning phenomena in plant cell cultures.
|
| [70] |
Jones AMP, Saxena PK. 2013. Inhibition of phenylpropanoid biosynthesis in
Artemisia annua L.: a novel approach to reduce oxidative browning in plant tissue culture.
|
| [71] |
Chen M, Li H, Zhang W, Huang L, Zhu J. 2022. Transcriptomic analysis of the differences in leaf color formation during stage transitions in
Populus ×
euramericana 'Zhonghuahongye'.
|
| [72] |
Coseteng MY, Lee CY. 1987. Changes in apple polyphenoloxidase and polyphenol concentrations in relation to degree of browning.
|
| [73] |
Xu Q, Yang XM, Wang GB, Cao FL. 2023. Transcriptome analysis of browning and non-browning callus of Ginkgo biloba. Molecular Plant Breeding 21:3237−44 |
| [74] |
Zhong J. 2019. Preliminary study of tissue culture system of Sapindus mukorossi Gaertn. Thesis. Beijing Forestry University, China. pp. 32−36 |
| [75] |
Aghayeh RNM, Abedy B, Balandari A, Samiei L, Tehranifar A. 2021. The first successful report: control of browning problem in
in vitro culture of iranian seedless barberry, a medicinally important species.
|
| [76] |
Tabiyeh DT, Bernard F, Shacker H. 2006. Investigation of glutathione, salicylic acid and GA
3 effects on browning in
Pistacia vera shoot tips culture.
|
| [77] |
Chen J. 2011. Study on browning control in
Cunninghamia lanceolata callus culture.
|
| [78] |
Rao H, Shao Z, Liu H, Wu Y, Qian P. 2015. Effect of browning inhibitors on callus subculture of phenolic compounds, enzyme and gene expression of grape. Plant Physiology Journal 51:1322−30 |
| [79] |
Haque M, Siddique AB, Islam SS. 2015. Effect of silver nitrate and amino acids on high frequency plants regeneration in barley (
Hordeum vulgare L.).
|
| [80] |
Xi Y, Zeng B, Huang H, Wang Y, Yang P. 2022. Resolving the browning during the establishment of the
in vitro propogation of
Prunus avium cv. 'Fuchen'.
|
| [81] |
Gao J, Xue J, Xue Y, Liu R, Ren X, et al. 2020. Transcriptome sequencing and identification of key callus browning-related genes from petiole callus of tree peony (
Paeonia suffruticosa cv. Kao) cultured on media with three browning inhibitors.
|
| [82] |
Meziani R, Jaiti F, Mazri MA, Hassani A, Ben Salem S, et al. 2016. Organogenesis of
Phoenix dactylifera L. cv. Mejhoul: influences of natural and synthetic compounds on tissue browning, and analysis of protein concentrations and peroxidase activity in explants.
|
| [83] |
Thomas TD. 2008. The role of activated charcoal in plant tissue culture.
|
| [84] |
Deng X, Huang J, Zhang M, Wei X, Song H, et al. 2023. Metabolite profiling and screening of callus browning-related genes in lotus (
Nelumbo nucifera).
|
| [85] |
Pompili V, Mazzocchi E, Moglia A, Acquadro A, Comino C, et al. 2023. Structural and expression analysis of polyphenol oxidases potentially involved in globe artichoke (
C. cardunculus var.
scolymus L.) tissue browning.
|
| [86] |
Wang H, Zhang S, Wang Z, Li D, Yan L, et al. 2024. Resistance index and browning mechanism of apple peel under high temperature stress.
|
| [87] |
Zhang K, Su J, Xu M, Zhou Z, Zhu X, et al. 2020. A common wild rice-derived
BOC1 allele reduces callus browning in
indica rice transformation.
|
| [88] |
Boudet AM. 2007. Evolution and current status of research in phenolic compounds.
|
| [89] |
Wei R, Zhang W, Li C, Hao Z, Huang D, et al. 2023. Establishment of Agrobacterium-mediated transformation system to
Juglans sigillata Dode 'Qianhe-7'.
|
| [90] |
Cho JS, Nguyen VP, Jeon HW, Kim MH, Eom SH, et al. 2016. Overexpression of
PtrMYB119, a R2R3-MYB transcription factor from
Populus trichocarpa, promotes anthocyanin production in hybrid poplar.
|
| [91] |
Duan J, Yu H, Yuan K, Liao Z, Meng X, et al. 2019. Strigolactone promotes cytokinin degradation through transcriptional activation of
CYTOKININ OXIDASE/DEHYDROGENASE 9 in rice.
|
| [92] |
Hao Z, Wu H, Zheng R, Li R, Zhu Z, et al. 2023. The plant peptide hormone phytosulfokine promotes somatic embryogenesis by maintaining redox homeostasis in
Cunninghamia lanceolata.
|
| [93] |
Ikeuchi M, Iwase A, Ito T, Tanaka H, Favero DS, et al. 2022. Wound-inducible WUSCHEL-RELATED HOMEOBOX 13 is required for callus growth and organ reconnection.
|
| [94] |
Yang W, Zhai H, Wu F, Deng L, Chao Y, et al. 2024. Peptide REF1 is a local wound signal promoting plant regeneration.
|
| [95] |
McFarland FL, Collier R, Walter N, Martinell B, Kaeppler SM, et al. 2023. A key to totipotency:
Wuschel-like homeobox 2a unlocks embryogenic culture response in maize (
Zea mays L.).
|
| [96] |
Hassani SB, Trontin JF, Raschke J, Zoglauer K, Rupps A. 2022. Constitutive overexpression of a conifer
WOX2 homolog affects somatic embryo development in
Pinus pinaster and promotes somatic embryogenesis and organogenesis in
Arabidopsis seedlings.
|
| [97] |
Zhu T, Moschou PN, Alvarez JM, Sohlberg JJ, Von-Arnold S. 2016.
WUSCHEL-RELATED HOMEOBOX 2 is important for protoderm and suspensor development in the gymnosperm Norway spruce.
|
| [98] |
Li Z, Qian W, Qiu S, Wang W, Jiang M, et al. 2024. Identification and characterization of the
WOX gene family revealed two
WUS clade members associated with embryo development in
Cunninghamia lanceolata.
|
| [99] |
Lee K, Park OS, Seo PJ. 2018. ATXR2 as a core regulator of
de novo root organogenesis.
|
| [100] |
Maulidiya AUK, Sugiharto B, Dewanti P, Handoyo T. 2020. Expression of somatic embryogenesis-related genes in sugarcane (
Saccharum officinarum L.).
|
| [101] |
Min L, Hu Q, Li Y, Xu J, Ma Y, et al. 2015. LEAFY COTYLEDON1-CASEIN KINASE I-TCP15-PHYTOCHROME INTERACTING FACTOR4 network regulates somatic embryogenesis by regulating auxin homeostasis.
|
| [102] |
Debernardi JM, Tricoli DM, Ercoli MF, Hayta S, Ronald P, et al. 2020. A GRF–GIF chimeric protein improves the regeneration efficiency of transgenic plants.
|
| [103] |
Yang E, Yang H, Li C, Zheng M, Song H, et al. 2022. Genome-wide identification and expression analysis of the
Aux/IAA gene family of the drumstick tree (
Moringa oleifera Lam.) reveals regulatory effects on shoot regeneration.
|
| [104] |
Xiong J, Zhang W, Zheng D, Xiong H, Feng X, et al. 2022. ZmLBD5 increases drought sensitivity by suppressing ROS accumulation in
Arabidopsis.
|
| [105] |
Liu S, Wang B, Li X, Pan J, Qian X, et al. 2019.
Lateral Organ Boundaries Domain 19 (
LBD19) negative regulate callus formation in
Arabidopsis.
|
| [106] |
Iwase A, Harashima H, Ikeuchi M, Rymen B, Ohnuma M, et al. 2017. WIND1 promotes shoot regeneration through transcriptional activation of
ENHANCER OF SHOOT REGENERATION1 in
Arabidopsis.
|
| [107] |
Wang X, Bi C, Wang C, Ye Q, Yin T, et al. 2019. Genome-wide identification and characterization of
WUSCHEL-related homeobox (
WOX) genes in
Salix suchowensis.
|
| [108] |
Wang K, Shi L, Liang X, Zhao P, Wang W, et al. 2022. The gene
TaWOX5 overcomes genotype dependency in wheat genetic transformation.
|
| [109] |
Liu B, Zhang J, Yang Z, Matsui A, Seki M, et al. 2018.
PtWOX11 acts as master regulator conducting the expression of key transcription factors to induce de novo shoot organogenesis in
poplar.
|
| [110] |
Lv J, Feng Y, Jiang L, Zhang G, Wu T, et al. 2023. Genome-wide identification of
WOX family members in nine Rosaceae species and a functional analysis of
MdWOX13-1 in drought resistance.
|
| [111] |
Permadi N, Akbari SI, Prismantoro D, Indriyani NN, Nurzaman M, et al. 2024. Traditional and next-generation methods for browning control in plant tissue culture: current insights and future directions.
|
| [112] |
Feng BS, Kang DC, Sun J, Leng P, Liu LX, et al. 2022. Research on melatonin in fruits and vegetables and the mechanism of exogenous melatonin on postharvest preservation.
|
| [113] |
Favre LC, dos Santos C, López-Fernández MP, Mazzobre MF, del Pilar Buera M. 2018. Optimization of β-cyclodextrin-based extraction of antioxidant and anti-browning activities from thyme leaves by response surface methodology.
|
| [114] |
Martínez-Hernández GB, Castillejo N, Artés-Hernández F. 2019. Effect of fresh-cut apples fortification with lycopene microspheres, revalorized from tomato by-products, during shelf life.
|
| [115] |
Xiao Y, He J, Zeng J, Yuan X, Zhang Z, et al. 2020. Application of citronella and rose hydrosols reduced enzymatic browning of fresh-cut taro.
|
| [116] |
Ranjith FH, Muhialdin BJ, Arroo R, Yusof NL, Mohammed NK, et al. 2022. Lacto-fermented polypeptides integrated with edible coatings for mango (
Mangifera indica L.) bio-preservation.
|
| [117] |
Julaeha E, Nurzaman M, Wahyudi T, Nurjanah S, Permadi N, et al. 2022. The development of the antibacterial microcapsules of
Citrus essential oil for the cosmetotextile application: a review.
|