Data/hora: 01/06/2024 15:58:19

Provedor de dados: 	64	
País: 	Brazil	
Título: 	Cryopreservation of coffee zygotic embryos: dehydration and osmotic rehydration	
Autores: 	Pinto,Maísa de Siqueira; Paiva,Renato; Silva,Diogo Pedrosa Corrêa da; Santos,Paulo Augusto Almeida; Freitas,Rodrigo Therezan de; Silva,Luciano Coutinho.	
Data: 	2016-08-01	
Ano: 	2016	
Palavras-chave: 	Coffea arabica L; Ex situ conservation; Embryos dehydration; Long-term storage; Gene bank.	
Resumo: 	ABSTRACT Conservation of plant genetic resources is important to prevent genetic erosion. Seed banks are the most common method of ex situ conservation; however, coffee seeds can not be stored by conventional methods. Cryopreservation is a viable alternative for long-term conservation of species that produce intermediate or recalcitrant seeds, as coffee. The aim of this work was to cryopreserve Coffea arabica L. cv Catuaí Vermelho IAC 144 zygotic embryos, and analyse the effects of dehydration prior cryopreservation and osmotic rehydration after thawing, in embryos germination and seedlings formation after cryopreservation. Prior to cryopreservation, different dehydration times (0, 15, 30, 60 and 120 min) were tested. Dehydrated embryos were cryopreserved in liquid nitrogen for 1 hour, and after thawing were rehydrated by osmotic solutions. Dehydrated and non-cryopreserved embryos were also analysed. The test with 2,3,5 triphenyl tetrazolium chloride (TTC) was used to evaluate the embryos viability. Non-dehydrated embryos did not survive after freezing. Embryos that were dehydrated until 20% of the moisture content did not germinate when osmotic rehydration was not performed. In contrast, cryopreserved embryos with the same moisture content presented 98% germination when they were rehydrated slowly in osmotic solution. According to tetrazolium tests, embryos presented maximum viability (75%) after dehydration for 60 minutes (23% moisture content). Therefore, coffee zygotic embryos (Coffea arabica L. cv. Catuaí Vermelho) can be successfully cryopreserved using physical dehydration in silica gel for 60 minutes (23% moisture content), followed by osmotic rehydration after thawing. This method allowed a germination of 98% of cryopreserved zygotic embryos.	
Tipo: 	Info:eu-repo/semantics/article	
Idioma: 	Inglês	
Identificador: 	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-70542016000400380	
Editor: 	Editora da Universidade Federal de Lavras	
Relação: 	10.1590/1413-70542016404007616	
Formato: 	text/html	
Fonte: 	Ciência e Agrotecnologia  v.40 n.4 2016	
Fonte: 	info:eu-repo/semantics/openAccess