Genetic homogeneity and high shoot proliferation in banana (Musa acuminata Colla) by altering medium thiamine level and sugar type

被引:13
作者
El-Mahdy, Marwa Talaat [1 ]
Youssef, Muhammad [2 ]
机构
[1] Assiut Univ, Fac Agr, Pomol Dept, Assiut 71526, Egypt
[2] Assiut Univ, Fac Agr, Genet Dept, Assiut 71526, Egypt
关键词
Banana (Musa acuminata Colla); Carbon source; Cavendish; Genetic fidelity; Multiplication rate; IN-VITRO PROPAGATION; SOMATIC EMBRYOGENESIS; CARBON-SOURCES; ISSR; MICROPROPAGATION; REGENERATION; SORBITOL; MARKERS; GROWTH; RAPD;
D O I
10.1007/s11627-019-10013-7
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
To enhance the multiplication rate in Musa acuminata Colla (banana; 'Grand Nain') organogenesis, higher amounts of thiamine along with different sugar types and concentrations were evaluated at the proliferation phase. Thiamine at 1, 10, 50, 100, and 200 mg L-1 was compared with 0.1 mg L-1 thiamine found in conventional Murashige and Skoog (MS) medium. Maximum proliferation of banana was induced with 100 mg L-1 thiamine. Additionally, 15, 30, and 45 g L-1 sucrose, glucose, fructose, and sorbitol combined with regular and optimal levels of thiamine were tested. Glucose at 30 g L-1 most improved shoot proliferation alone and enhanced shoot proliferation further, when combined with 100 mg L-1 thiamine, followed by sucrose and fructose, whereas sorbitol completely inhibited growth and caused tissue browning. All evaluated vegetative traits were significantly affected by sugar type and concentration, and thiamine levels, unlike the photosynthetic pigments. Moreover, genetic stability of the plants recovered from the enhanced protocol was confirmed by inter-simple sequence repeats (ISSR) and randomly amplified polymorphic DNA (RAPD) analysis. A total of 230 bands generated by both marker types were monomorphic for the randomly selected regenerated plants, compared with their mother plant. Thus, the proliferation medium supplemented with 30 g L-1 glucose and 100 mg L-1 thiamine could be recommended for banana organogenesis. Results herein are of great importance and helpful in enhancing the commercial in vitro propagation protocols of banana, without the need of increasing the number of subcultures, which can cause somaclonal variation.
引用
收藏
页码:668 / 677
页数:10
相关论文
共 54 条
[11]  
Chowdhury MMH, 2012, INT J SUSTAIN CROP P, V7, P12
[12]   Influence of carbon source on shoot multiplication and adventitious bud regeneration in in vitro beech cultures [J].
Cuenca, B ;
Vieitez, AM .
PLANT GROWTH REGULATION, 2000, 32 (01) :1-12
[13]  
Ebadi M, 2017, BIOSCI BIOTECH RES C, V10, P288
[14]   The effects of silver nitrate and different carbohydrate sources on somatic embryogenesis in Coffea canephora [J].
Fuentes, SRL ;
Calheiros, MBP ;
Manetti, J ;
Vieira, LGE .
PLANT CELL TISSUE AND ORGAN CULTURE, 2000, 60 (01) :5-13
[15]  
George EF., 2008, Plant Propagation by Tissue Culture, V3rd, P115, DOI DOI 10.1007/978-1-4020-5005-3_4
[16]   Thiamine in plants: Aspects of its metabolism and functions [J].
Goyer, Aymeric .
PHYTOCHEMISTRY, 2010, 71 (14-15) :1615-1624
[17]   AMPLIFICATION OF DNA MARKERS FROM EVOLUTIONARILY DIVERSE GENOMES USING SINGLE PRIMERS OF SIMPLE-SEQUENCE REPEATS [J].
GUPTA, M ;
CHYI, YS ;
ROMEROSEVERSON, J ;
OWEN, JL .
THEORETICAL AND APPLIED GENETICS, 1994, 89 (7-8) :998-1006
[18]  
Hossain M. J., 2009, J BIOSCIENCE, V17, P83
[19]  
Hussein N., 2012, African Journal of Biotechnology, V11, P9001
[20]   In vitro propagation and assessment of genetic stability of acclimated plantlets of Cornus alba L. using RAPD and ISSR markers [J].
Ilczuk, Agnieszka ;
Jacygrad, Ewelina .
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-PLANT, 2016, 52 (04) :379-390