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      LED Lights Affecting Morphogenesis and Isosteroidal Alkaloid Contents in Fritillaria cirrhosa D. Don—An Important Chinese Medicinal Herb

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          Abstract

          Investigations were carried out to study the effects of light-emitting diode (LED) lights on growth and development of isosteroidal alkaloids in embryogenic calli of Fritillaria cirrhosa D. Don, an important traditional Chinese medicine herb. Calli were cultured in glass bottles, each containing 100 mL of Murashige and Skoog’s basal medium supplemented with 2% sucrose and 0.4% gellan gum powder, a gelling agent. These bottles were incubated in a specially designed plant growth chamber equipped with eight different LED lights consisting of single or combinations of four different light spectra emitting blue (450 nm), green (525 nm), red (660 nm), and far-red (730 nm) light. After three months of incubation, morphological changes in embryogenic calli were recorded, and LC-MS/MS analysis of cultures was carried out for peimisine, sipeimine, peiminine, and peimine. The highest number of somatic embryos and the maximum fresh weight was recorded in calli incubated under red (9R), infrared (9IR), and a combination of red+blue+infrared (3R3B3IR), respectively, in decreasing order. The highest contents of peimisine, peiminine, and peimine were recorded under red (9R) and infrared (9IR) lights, respectively. Eight LED lights had significant effects on the morphogenesis of embryogenic calli of F. cirrhosa D. Don and contents of isosteroidal alkaloids.

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          A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures

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            Cryptochromes Interact Directly with PIFs to Control Plant Growth in Limiting Blue Light.

            Sun-loving plants have the ability to detect and avoid shading through sensing of both blue and red light wavelengths. Higher plant cryptochromes (CRYs) control how plants modulate growth in response to changes in blue light. For growth under a canopy, where blue light is diminished, CRY1 and CRY2 perceive this change and respond by directly contacting two bHLH transcription factors, PIF4 and PIF5. These factors are also known to be controlled by phytochromes, the red/far-red photoreceptors; however, transcriptome analyses indicate that the gene regulatory programs induced by the different light wavelengths are distinct. Our results indicate that CRYs signal by modulating PIF activity genome wide and that these factors integrate binding of different plant photoreceptors to facilitate growth changes under different light conditions.
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              Recent progress in the understanding of tissue culture-induced genome level changes in plants and potential applications.

              In vitro cell and tissue-based systems have tremendous potential in fundamental research and for commercial applications such as clonal propagation, genetic engineering and production of valuable metabolites. Since the invention of plant cell and tissue culture techniques more than half a century ago, scientists have been trying to understand the morphological, physiological, biochemical and molecular changes associated with tissue culture responses. Establishment of de novo developmental cell fate in vitro is governed by factors such as genetic make-up, stress and plant growth regulators. In vitro culture is believed to destabilize the genetic and epigenetic program of intact plant tissue and can lead to chromosomal and DNA sequence variations, methylation changes, transposon activation, and generation of somaclonal variants. In this review, we discuss the current status of understanding the genomic and epigenomic changes that take place under in vitro conditions. It is hoped that a precise and comprehensive knowledge of the molecular basis of these variations and acquisition of developmental cell fate would help to devise strategies to improve the totipotency and embryogenic capability in recalcitrant species and genotypes, and to address bottlenecks associated with clonal propagation. © Springer-Verlag 2011
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                Author and article information

                Journal
                Plants (Basel)
                Plants (Basel)
                plants
                Plants
                MDPI
                2223-7747
                13 October 2020
                October 2020
                : 9
                : 10
                : 1351
                Affiliations
                [1 ]Department of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, China Medical University, Taichung 40402, Taiwan; ferny1010@ 123456yahoo.com.tw (C.-C.C.); crw@ 123456mail.cmu.edu.tw (C.-R.W.)
                [2 ]Department of Chemistry, National Chung-Hsing University, Taichung 40227, Taiwan; mrlee@ 123456dragon.nchu.edu.tw (M.-R.L.); qaznancy@ 123456gmail.com (H.-J.K.)
                [3 ]Nin Jiom Pharmaceutical Co. Ltd., Taipei 108024, Taiwan; patricia@ 123456ninjiom.com.tw
                [4 ]Department of Applied Chemistry, Chaoyang University of Technology, Taichung 41349, Taiwan; hstsay@ 123456cyut.edu.tw
                [5 ]Department of Golden-Ager Industry Management, Chaoyang University of Technology, Taichung 41349, Taiwan
                Author notes
                [* ]Correspondence: dcagrawal@ 123456gm.cyut.edu.tw (D.C.A.); changhungchi@ 123456cyut.edu.tw (H.-C.C.); Tel.: +886-4-23323000 (ext. 4238) (D.C.A.); +886-4-23323000 (ext. 5345) (H.-C.C.)
                Author information
                https://orcid.org/0000-0002-7036-5035
                Article
                plants-09-01351
                10.3390/plants9101351
                7602057
                33066243
                fed45490-95b0-41ec-ad76-d405ff3c4633
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 12 August 2020
                : 07 October 2020
                Categories
                Article

                fritillaria cirrhosa d. don,alkaloid content,callus,in vitro culture,led lights,light intensity

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