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苹果砧木新品种鲁砧1号离体叶片高效不定植株再生

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[目的]建立苹果半矮化砧木新品种鲁砧1号离体叶片高效不定梢再生技术体系,为该砧木快繁和遗传改良奠定技术基础.[方法]以鲁砧1号无菌苗离体叶片为外植体,研究碳源、细胞分裂素种类和质量浓度对叶片不定梢再生的影响;以不定梢为试材,研究基本培养基、蔗糖质量浓度对不定梢生根的影响.[结果]MS添加较低质量浓度(0.6 mg·L-1)细胞分裂素(TDZ)时,碳源物质为D-山梨醇的叶片不定梢再生率显著高于蔗糖;其他激素处理下,D-山梨醇和蔗糖之间叶片不定梢再生率无显著差异.两种碳源上的平均每叶不定芽(梢)数,都表现较高细胞分裂素质量浓度处理高于或显著高于较低细胞分裂素质量浓度处理,以TDZ质量浓度为1 mg·L-1时产生的不定芽数最多,平均每叶不定芽数为3.8~4个.在不定芽诱导培养基上,6-苄基氨基嘌呤(BA)比TDZ更容易诱导产生直接伸长生长的不定梢.不定梢生根率和平均每株生根条数,两种基本培养基及两个蔗糖质量浓度之间都表现差异不显著,但以1/4MS基本培养基和20g·L-1蔗糖组合的生根培养基上获得的生根率和单株生根条数最高,分别超过93%和5.8.[结论]鲁砧1号离体叶片容易诱导再生不定芽和不定梢生根,诱导叶片不定芽再生最佳培养基为MS添加1 mg·L-1 TDZ、0.3 mg·L-1 IBA和30 g·L-1蔗糖,最佳生根培养基为1/4MS添加0.3~0.5 mg·L-1 IBA和20 g·L-1蔗糖.
High-efficiency regeneration from leaf explants of apple rootstock Lu-zhen 1
[Objective]Apple rootstocks are used to influence precocity,tree size,fruit quality,yield ef-ficiency,mineral uptake and disease related to replanting,and to withstand adverse environmental con-ditions.Dwarfing rootstocks play an important role in developing modern orchards.New apple root-stock cultivar Luzhen 1 is a semi-dwarfing rootstock which was selected and released by Shandong In-stitute of Pomology.This new rootstock has similar effect on tree size to M.26.It can be propagated clonally and has good grafting compatibility with many scion cultivars.The purpose of this paper is to establish a system of high-efficiency plant regeneration from leaf explants of Luzhen 1 and to provide a method for commercial propagation of the plant and genetic improvement using biotechnological meth-ods.[Methods]In mid-to-late April,semi-lignified healthy shoots of Luzhen 1 were used as explants for culture of in vitro sterile plantlets.The leaves from the aseptic plantlets were cultured to induce ad-ventitious shoots.Through the above experiments,the effects of carbon source and type and concentra-tion of cytokinin on leaf regeneration were studied.Further,the effects of basic medium and sucrose concentration on rooting of adventitious shoots were also studied.[Results]The axillary buds on semi-lignified shoots broke and extended to form aseptic green plantlets,after culturing on the axillary bud initiation medium for 3 weeks.These plantlets grew well on the secondary proliferation medium with good proliferation and elongation growth,and the monthly multiplication ratio was above 5.0,indicat-ing easy multiplication and propagation of Luzhen 1.In the two carbon sources tested,D-sorbitol and sucrose were both effective in inducing adventitious bud.Except that the adventitious bud regeneration rate on D-sorbitol was significantly higher than that on sucrose at a low cytokinin(TDZ)concentration of 0.6 mg·L-1,there was no significant difference in the adventitious bud regeneration rate between the two carbon sources in other treatments,both of which were as high as 90%.For the average number of adventitious buds per leaf,there was no significant difference between the two carbon sources under the same type and concentration of cytokinin.These results indicate that the carbon source is not strictly re-quired for adventitious bud regeneration from the isolated leaves of the new rootstock cultivar.Under the same carbon source,the adventitious bud regeneration rate and average bud number per leaf were the lowest when TDZ was at 0.6 mg·L-1,and the results were consistent for the two carbon sources.When the carbon source in the medium was D-sorbitol,there was no significant difference in the regen-eration rate of adventitious buds between TDZ and BA,and between different concentrations.However,the average number of adventitious buds per leaf at 1 mg·L-1 concentration of TDZ was significantly higher than that at 0.6 mg·L-1,while there was no significant difference between the two concentrations of BA.When the carbon source in the medium was sucrose,the regeneration rate of TDZ at 0.6 mg·L-1 was significantly lower than that of other treatments,but the average number of adventitious buds per leaf was not significantly different among different treatments.On adventitious-bud induction medium,cytokinin BA was more effective than TDZ in inducing the elongated and growing adventitious shoots,while the adventitious buds induced by TDZ needed to be transferred to the proliferation medium with-out TDZ in order to obtain such adventitious shoots.The best medium for inducing adventitious buds from leaves was MS medium with 1 mg·L-1 TDZ,0.3 mg·L-1 IBA and 30 g·L-1 sucrose.After root in-duction culture for 12 days,the emergence of early adventitious root protrusions could be observed.Af-ter culture for 18 days,the formation of short roots became obvious,with final root formation rates above 88%.After culture for 22 days,no new adventitious roots were induced and root elongation growth could be observed.All the eight rooting media tested could successfully induce rooting from the adventitious shoots,but the rooting rate varied greatly,while the average number of roots per shoot had no significant difference.Independent of the concentration of IBA,the basic medium of 1/4 MS with the lower sucrose(20 g·L-1)was more effective to increase rooting rate and the number of roots per shoot than that with a higher sucrose(30 g·L-1).In addition to 0.3 mg·L-1 IBA,rooting rate on 20 g·L-1 sucrose was significantly higher than that on 30 g·L-1 sucrose.On the basic medium of 1/2 MS,there was no significant difference in rooting rate and number of roots per plant between the two sucrose con-centrations or between the two IBA concentrations.The rooting rate of the four treatments could be higher than 70%,indicating that,on the basic medium of 1/2 MS,there was no strict requirement on su-crose or IBA concentration for the adventitious rooting in Luzhen 1.The results indicated that adventi-tious shoots of Luzhen 1 root easily.The optimal rooting medium was 1/4 MS supplemented with 0.3-0.5 mg·L-1 IBA and 20 g·L-1 sucrose.The rooting rate was over 93%and the average number of roots per plant was 5.9.[Conclusions]It is relatively easy to induce bud regeneration from leaf explants and in vitro rooting from the adventitious shoots in the new semi-dwarfing apple rootstock cultivar Luzhen 1.Based on this study,the optimal medium for adventitious bud induction of Luzhen 1 is MS+1 mg·L-1 TDZ+0.3 mg·L-1 IBA+30 g·L-1 sucrose,and the best medium for in vitro rooting from the adventitious shoots is 1/4MS+0.3-0.5 mg·L-1 IBA+20 g·L-1 sucrose.

AppleDwarfing rootstockLeaf explantShoot inductionIn vitro rooting from adventi-tious shoots

王海波、王森、郑文燕、王平、何晓文、常源升、何平、孙清荣、李林光

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山东省果树研究所,山东泰安 271000

山东烟富农业科技有限公司,山东烟台 265699

苹果 矮化砧木 离体叶片 叶片不定梢再生 不定梢生根

山东省重点研发计划现代农业产业技术体系专项山东省自然科学基金山东省农业科学院农业科技创新工程

2023LZGCQY009CARS-27ZR2021MC045CXGC2023A28

2024

果树学报
中国农业科学院郑州果树研究所

果树学报

CSTPCD北大核心
影响因子:1.486
ISSN:1009-9980
年,卷(期):2024.41(9)
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