Buhara Yücesan

Prof. Dr. Buhara Yücesan

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Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 January 2024 in Plant Cell, Tissue and Organ Culture (PCTOC)
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Journal Article
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NBNida Bayhan
Nida Bayhan
BYBuhara Yücesan
Buhara Yücesan
Vitrification is one of the most significant issues encountered in plant tissue culture applications. It diminishes the quality of in vitro plants, causing their leaves and stems to appear watery and translucent, and it may impede the success of the acclimatization step. In this respect, this study investigates the impact of sucrose and 6-Benzylaminopurine (BAP) concentrations on shoot regeneration and vitrification development in Aronia melanocarpa, known for its high antioxidant content and health benefits. Initially, the presence of BAP, in combination with varying sucrose concentrations, leads to a substantial increase in shoot number, and the largest number (7 shoots per nodal explant) was observed in the Murashige and Skoog (MS) medium containing 3% sucrose and 5.0 mg/L BAP. Furthermore, sucrose concentration plays a crucial role in shoot growth, with higher concentrations promoting more extensive shoot development. However, when 3% sucrose was combined with higher BAP (from 1.0- to 5.0 mg/L), an increased incidence of vitrification was observed over time. Interestingly, lower sucrose concentrations (1% or 2%) combined with 0.5 mg/L or 2.5 mg/L BAP initially delayed vitrification but eventually led to its occurrence. Microscopic analysis of leaf samples with varying levels of vitrification indicates significant differences in the density of stomata, further confirming the detrimental impact of vitrification on cellular structures and physiological processes. The recovery of vitrified plants was evaluated using different growth media combinations. The absence of BAP in the medium led to higher recovery percentages (min 96%) without necrosis, while the addition of 0.5 mg/L BAP promoted shoot growth but potentially inhibited root development. It has been found that media with 1 mg/L BAP and either 10 g/L or 20 g/L sucrose, as well as media with 30 g/L sucrose and 0.5 mg/L BAP, are the most suitable for efficient shoot regeneration with minimal vitrification risk. However, increasing BAP levels for faster shoot regeneration also raises the risk of vitrification. During acclimatization, vitrified plants exhibited stunted shoot growth, shorter and narrower leaves, reduced root numbers and lengths, and decreased survival rates, particularly under lower humidity conditions. The cultivation period required for the recovery of the crop was determined to be 6 weeks under greenhouse conditions for a sustainable plant propagation.

18 August 2025 in Plant Cell, Tissue and Organ Culture (PCTOC)
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VSValbona Sota
Valbona Sota
HWHannes Wilms
Hannes Wilms
BYBuhara Yücesan
Buhara Yücesan
YMYeşim Yalçin Mendi
Yeşim Yalçin Mendi
BCBruce Christie
Bruce Christie
Maurizio LambardiMaurizio Lambardi
Maurizio Lambardi
Commercial micropropagation plays a crucial role in increasing the production of many economically important fruit crops worldwide, including Europe. The focus has been on many woody horticultural species, such as stone and pome fruits, berries, nuts, and palms. This paper presents an updated overview of the European commercial micropropagation landscape, highlighting the countries currently operating in this sector, crop targets, and the distribution of micropropagation companies based on recent survey data. In Europe and the broader Mediterranean basin, Italy, Spain, Türkiye, and Germany emerge as the leading contributors to the large-scale in vitro production of woody fruit species, based on the number of operating commercial companies and efforts to adopt new technology. Despite this progress, several challenges limit the scalability and sustainability of in vitro propagation systems, and their expansion in underrepresented countries. These main issues include species recalcitrance, high labour and infrastructure costs, further improvement of stock maintenance capacity, logistical issues in plantlet shipment, and barriers related to intellectual property rights. To address these challenges, this paper discusses solutions such as utilizing automation and robotics, exploring new compounds to enhance micropropagation rates, and using European funding opportunities. Furthermore, being involved in pan-European cooperation and technology transfer networks is also encouraged. The COST Action 21157 “CopyTree: European Network for Innovative Woody Plant Cloning” is discussed as a practical example of collaboration in harmonizing protocols for woody plant cloning and facilitating knowledge sharing among research groups with varying levels of experience in the field. Future advancements in the micropropagation sector will depend on the investment in automation and innovative technologies, combined with policy alignment with EU standards on a broader international level, and regional development strategies.


1 January 2015 in TURKISH JOURNAL OF AGRICULTURE AND FORESTRY
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Journal Article
Closed access
BYBuhara Yücesan
Buhara Yücesan
AMAliyu Mohammed
Aliyu Mohammed
MAMerve Arslan
Merve Arslan
EGEkrem Gurel
Ekrem Gurel

1 October 2014 in In Vitro Cellular & Developmental Biology - Plant
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Wolfgang KreisWolfgang Kreis
Wolfgang Kreis
BHBirgit Haug
Birgit Haug
BYBuhara Yücesan
Buhara Yücesan