Report of Naturally occurring albinism in Asparagus racemosus Willd.: A three years observation
DOI:
https://doi.org/10.36808/if/2025/v151i6/170800Keywords:
No Keywords.Abstract
No Abstract.
References
Akhtar S., Gupta A.K., Naik B., Kumar V., Ranjan R., Jha A.K., Rather M.A. and Rustagi S. (2024). Exploring pharmacological properties and food applications of Asparagus racemosus (Shatavari). Food Chemistry Advances, 4: 100689. DOI: https://doi.org/10.1016/j.focha.2024.100689
Chavan S., Keerthika A., Jha A., Handa A.K., Newaj R. and Dhyani S. (2016). A note on albinism in Madhuca latifolia J.F. Gmel. Indian Forester, 142: 400-402.
Chintala S.R., Nagesh K. and Pruthiviraj M. (2001). Occurrence of Albino seedlings in Azadirachta indica (Meliaceae). J. Non-Timber Forest Products, 8: 229-230. DOI: https://doi.org/10.54207/bsmps2000-2001-5YH8DF
Dong S., Fan M., Qin Q., Zhang Z., Duan K., Cosić T., Raspor M. and Ni D.-A. (2024). Natural Albino Mutant of Daylily (Hemerocallis spp.) Reveals a Link between Drought Sensitivity and Photosynthetic Pigments Metabolism. Frontiers in Bioscience-Landmark, 29.60. DOI: https://doi.org/10.31083/j.fbl2902060
Falbel T.G. and Staehelin L.A. (1996). Partial blocks in the early steps of the chlorophyll synthesis pathway: A common feature of chlorophyll b-deficient mutants. Physiologia Plantarum, 97. 311-320. DOI: https://doi.org/10.1034/j.1399-3054.1996.970214.x
Gotoh E., Suetsugu N., Yamori W., Ishishita K., Kiyabu R., Fukuda M., Higa T., Shirouchi B. and Wada M. (2018). Chloroplast Accumulation Response Enhances Leaf Photosynthesis and Plant Biomass Production. Plant Physiology, 178:1358-1369. DOI: https://doi.org/10.1104/pp.18.00484
Gunaga R.P. and Vasudeva R. (2011). Albino wildlings in Dysoxylum Malabaricum Bedd., a critically endangered tree species of Western Ghats. J. Non-Timber Forest Products, 18: 337-340. DOI: https://doi.org/10.54207/bsmps2000-2011-7H49ES
Gunaga R., Wange S.S., Mirgal A., Rane A.D., Narkhede S.S. and Bhave S.G. (2013). A Note on Albinism in Saraca asoca (Roxb.) De Wild. Indian Forester, 139: 471-472.
Hung C.-Y., Zhang J., Bhattacharya C., Li H., Kittur F.S., Oldham C.E., Wei X., Burkey K.O., Chen J. and Xie J. (2021). Transformation of long-lived albino Epipremnum aureum 'Golden Pothos and restoring chloroplast development. Frontiers in Plant Science, 12:647507. DOI: https://doi.org/10.3389/fpls.2021.647507
Jose P. and Pandurangan A.G. (2011). Occurrence of Albino seedlings and its genetic significance in Gluta travancorica Bedd. Indian Journal of Forestry, 34: 377-378. DOI: https://doi.org/10.54207/bsmps1000-2011-6T59M6
Kader S.A. and Seethalakhsmi K.K. (2000). Atypical seedlings in Hopea parviflora, Bedd. Indian Forester, 126: 308-310.
Klíčová Š., Šebánek J., Hudeová M., H.V.V. and Vlašínová H. (2002). The effect of fluridone and flurochloridone on the incidence of albinism in pea (Pisum sativum) and on the abscission of leaves of privet (Ligustrum vulgare). Rostlinná Výroba, 48: 255-260. DOI: https://doi.org/10.17221/4237-PSE
Kumari M., Clarke H.J., Small I. and Siddique K.Η.Μ. (2009). Albinism in Plants: A Major Bottleneck in Wide Hybridization, Androgenesis and Doubled Haploid Culture. Critical Reviews in Plant Sciences, 28: 393-409. DOI: https://doi.org/10.1080/07352680903133252
Le L.M., Wakana A., Sakai K., Mizunoe Y., Kajiwara K., Kajihara S. and Ozaki Y. (2019). Inheritance of albinism in grapefruit (Citrus paradisi Macf.; al, al,) and 'Hanayu' (C. hanaju hort. ex Shirai; al, al,). Journal of Agriculture Science and Botany, 3: 1-5.
Lekshmi R., Gunaga R.P., Thakur N.S., Huse S.A. and Hegde Η.Τ. (2024). Recurrence of branch albinism in Tabernaemontana divaricata. Current Science, 127: 1007.
Nagesh K. and Kardam T.S. (2002). Occurrence of Albino Seedlings in Acacia nilotica (Linn.) Willd. Mimosaceae. Indian Forester 128:1043-1044. DOI: https://doi.org/10.54207/bsmps1000-2002-10Y57T
Nagesh K., Ramesh M., Kumar V. and Bhanja M. (2007). Occurrence of Albino and tricotyledonous seedlings in Eucalyptus citriodora Hook. (Myrtaceae). Indian Forester, 133: 279-281.
Patil V., Patil M. and Narkhede S. (2015). Albino Wildling of Tabernaemontana alternifolia L. and a Review of Albinism in Forest Plants in India. Journal of Tree Sciences, 34: 1-10.
Peirce G.J. (1901). Studies on the coast redwood, Sequoia sempervirens Endl, San Francisco, The Academy.
Pittermann J., Cowan J., Kaufman N., Baer A., Zhang E. and Kuty D. (2018). The water relations and xylem attributes of albino redwood shoots (Sequioa sempervirens (D. Don.) Endl.). PLOS ONE, 13: e0191836. DOI: https://doi.org/10.1371/journal.pone.0191836
Rao P., Murti S. and Venkaiah K. (1999), Albinism in Artocarpus integrifolia Linn. f.- A case study. Indian Forester, 125: 1095-1098.
Ruppel N.J., Logsdon C.A., Whippo C.W., Inoue K. and Hangarter R.P. (2010). A Mutation in Arabidopsis SEEDLING PLASTID DEVELOPMENT1 Affects Plastid Differentiation in Embryo-Derived Tissues during Seedling Growth. Plant Physiology, 155: 342-353. DOI: https://doi.org/10.1104/pp.110.161414
Sharmila K.P., Kumar Bhandary B., Fernandes R., Kumari N.S.. Bhat V.S., Shetty K.J., Jose J.M. and Peter A.J. (2018). Radioprotective potential of Asparagus racemosus root extract and isoprinosine against electron beam radiation-induced DOI: https://doi.org/10.4103/jnsbm.JNSBM_225_17
immunosupression and oxidative stress in swiss albino mice. Journal of Natural Science, Biology and Medicine, 9: 242-246,
Shi K., Gu J., Guo H., Zhao L., Xie Y., Xiong H., Li J., Zhao S., Song X. and Liu L. (2017). Transcriptome and proteomic analyses reveal multiple differences associated with chloroplast development in the spaceflight-induced wheat albino mutant mta. PLoS One, 12: e0177992. DOI: https://doi.org/10.1371/journal.pone.0177992
Silva L.A.S., Sampaio V.F., Barbosa L.C.S., Machado M., Flores-Borges D.N.A., Sales J.F., De Oliveira D.C., Mayer J.L.S., Kuster V.C. and Rocha D.I. (2020). Albinism in plants -far beyond the loss of chlorophyll: Structural and physiological aspects of wild-type and albino royal poinciana (Delonix regia) seedlings. Plant Biology, 22: 761-768. DOI: https://doi.org/10.1111/plb.13146
Takeuchi Y., Kikuchi S. and Diway B. (2020). Albinism and inbreeding depression in seedlings of the tropical tree, Shorea laxa. Journal of Forest Research, 25:413-419. DOI: https://doi.org/10.1080/13416979.2020.1796897
Vadivelan R., Gopala Krishnan R. and Kannan R. (2019). Antidiabetic potential of Asparagus racemosus Willd leaf extracts through inhibition of a-amylase and a-glucosidase. J Tradit Complement Med., 9: 1-4. DOI: https://doi.org/10.1016/j.jtcme.2017.10.004
Wang Y., Wang C., Zheng M., Lyu J., Xu Y., Li X., Niu M., Long W., Wang D., Wang H., Terzaghi W., Wang Y. and Wan J. (2016). WHITE PANICLE1, a Val-tRNA Synthetase Regulating Chloroplast Ribosome Biogenesis in Rice, Is Essential for Early Chloroplast Development. Plant Physiology, 170: 2110-2123. DOI: https://doi.org/10.1104/pp.15.01949
Xiong D., Huang J., Peng S. and Li Y. (2017). A few enlarged chloroplasts are less efficient in photosynthesis than a large population of small chloroplasts in Arabidopsis thaliana. Scientific Reports, 7:5782. DOI: https://doi.org/10.1038/s41598-017-06460-0
Yan J., Liu B., Cao Z., Chen L., Liang Z., Wang M., Liu W., Lin Y.E. and Jiang B. (2022). Cytological, genetic and transcriptomic characterization of a cucumber albino mutant. Frontiers in Plant Science, 13: 1047090. DOI: https://doi.org/10.3389/fpls.2022.1047090
Zhao Y., Yang P., Cheng Y., Liu Y., Yang Y. and Liu Z. (2023). Insights into the physiological, molecular, and genetic regulators of albinism in Camellia sinensis leaves. Frontiers in Genetics 14:1219335 DOI: https://doi.org/10.3389/fgene.2023.1219335
Downloads
Downloads
Published
How to Cite
Issue
Section
License
Unless otherwise stated, copyright or similar rights in all materials presented on the site, including graphical images, are owned by Indian Forester.
