Exogenous Catalase and Pyruvate Dehydrogenase Improve Survival and Regeneration and Affect Oxidative Stress in Cryopreserved Dendrobium nobile Protocorm-like Bodies.

低温保存 生物 生物化学 抗氧化剂 玻璃化 脯氨酸 食品科学 谷胱甘肽 脂质过氧化 二甲基亚砜
作者
Wei Di,Mengxue Jia,Jin Xu,Bingling Li,Yan Liu
出处
期刊:Cryo letters [Cryo-Letters]
卷期号:38 (3): 228-238 被引量:5
标识
摘要

Background Reactive oxygen species (ROS)-induced oxidative damage is responsible for viability loss in plant tissues following cryopreservation. Antioxidants may improve viability by preventing or repairing the injury. Objective This work aimed at studying the effect of catalase (CAT) and pyruvate dehydrogenase (PDH), which are involved in ROS metabolism and are differentially expressed during pollen cryopreservation, for cryopreservation of Dendrobium nobile Lindl. 'Hamana Lake Dream' protocorm-like bodies (PLBs). Materials and methods Different concentrations of exogenous CAT or PDH were added at the loading, PVS2 treatment, unloading steps during vitrification-cryopreservation of PLBs. Their survival and regeneration were evaluated and correlated with physiological oxidative indexes. Results PLB survival increased significantly when CAT and PDH were added separately to the unloading solution at a suitable concentration. CAT at 400 U·ml-1 increased PLB survival and regeneration by 33.5 and 14.6 percent respectively. It had no impact on the production of superoxide anion radical (·O2-) and on superoxide dismutase (SOD) activity, but it reduced the hydrogen peroxide (H2O2) and malondialdehyde (MDA) contents and enhanced ascorbic acid (AsA) and endogenous CAT levels compared to PLBs cryopreserved using the standard vitrification protocol (CK1). PDH at 0.1 U·ml-1 significantly improved PLB survival (by 2.5 percent), but it had no marked effect on regeneration compared to the CK1 group. It induced the same variations in ·O2-, AsA and endogenous CAT levels that were observed following CAT addition. However, PDH did not affect the H2O2 and MDA content but significantly increased SOD activity. Conclusion These results indicate that the addition of 400 U·ml-1 CAT and 0.1 U·ml-1 PDH at the unloading step increased survival of cryopreserved PLBs and that this improvement was associated with scavenging of H2O2 and the repair of oxidative damage. Exogenous CAT also significantly improved PLB regeneration after cryopreservation, while PDH had no obvious effect. The effect of exogenous CAT on PLB survival and regeneration was stronger than that of PDH, which may be due to the increased SOD activity by PDH addition.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
今天不熬夜完成签到 ,获得积分10
2秒前
3秒前
123完成签到 ,获得积分10
5秒前
象象完成签到 ,获得积分10
7秒前
采采完成签到,获得积分10
7秒前
嘟嘟52edm完成签到 ,获得积分10
10秒前
Mike完成签到,获得积分10
12秒前
16秒前
无情的聋五完成签到 ,获得积分10
21秒前
六六发布了新的文献求助10
22秒前
晃悠悠的可乐完成签到 ,获得积分10
23秒前
1111完成签到,获得积分10
24秒前
无尘完成签到 ,获得积分10
25秒前
胖胖完成签到 ,获得积分0
25秒前
安风完成签到 ,获得积分10
26秒前
28秒前
sweetrumors完成签到,获得积分10
30秒前
阳菲完成签到 ,获得积分10
31秒前
南攻完成签到,获得积分10
31秒前
keyanlv完成签到,获得积分10
33秒前
风雨晴鸿完成签到 ,获得积分10
35秒前
久伴久爱完成签到 ,获得积分10
36秒前
小徐完成签到 ,获得积分10
36秒前
安然完成签到 ,获得积分10
41秒前
44秒前
buerzi完成签到,获得积分10
45秒前
BAEK完成签到,获得积分10
45秒前
YMW发布了新的文献求助10
48秒前
49秒前
wzk完成签到,获得积分10
49秒前
Juzco完成签到 ,获得积分10
50秒前
racill完成签到 ,获得积分10
51秒前
LaixS完成签到,获得积分10
51秒前
Perrylin718完成签到,获得积分10
52秒前
要笑cc完成签到,获得积分10
53秒前
54秒前
宣宣宣0733完成签到,获得积分0
55秒前
辞旧完成签到,获得积分10
56秒前
胡质斌完成签到,获得积分10
57秒前
温暖的如冰完成签到,获得积分10
59秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Developing Genetic Editing Tools for Lysobacter 2000
卤化钙钛矿人工突触的研究 2000
Моделирование процессов самоорганизации в кристаллообразующих системах 1000
History of U.S. Space Surveillance and Satellite Cataloging 1000
Signals, Systems, and Signal Processing 610
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6519017
求助须知:如何正确求助?哪些是违规求助? 8311648
关于积分的说明 17770071
捐赠科研通 5621007
什么是DOI,文献DOI怎么找? 2926629
邀请新用户注册赠送积分活动 1903434
关于科研通互助平台的介绍 1764139