应用柑橘异源四倍体杂种花粉生产瘪籽沙田柚果实

以3个柑橘异源四倍体体细胞杂种(即四倍体粗柠檬与哈姆林甜橙体细胞杂种,简称"HR";酸柚与粗柠檬体细胞杂种,简称"SR";墨西哥来檬与伏令夏甜橙体细胞杂种,简称"KV")为父本,分别与二倍体单胚性沙田柚进行有性杂交,在生产上获得瘪籽沙田柚果实,并对果实品质进行分析(以四季柚花粉亲本为对照)。结果表明:授予柑橘异源四倍体杂种花粉的果实种子败育十分明显,果实瘪籽率达41.4%～96.0%,与对照间的差异极显著(P0.01);但果实单果重、果肉重、果皮重、果皮厚和果形指数与对照间无显著性差异(P0.05);果实可溶性固形物、全糖、Vc和可滴定酸含量与对照也无明显变化,且较适合于瘪籽沙田柚果实生产的体细胞杂种是HR和SR。     

哈姆林甜橙与粗柠檬体细胞杂种的育性

对异源四倍体柑桔体细胞杂种“哈姆林甜橙+粗柠檬”及其亲本的花粉活力、花器官发育、花器官形态发生与花粉母细胞减数分裂四分体阶段进行了观测和统计.结果发现“哈姆林甜橙+粗柠檬”的花粉染色活力、萌发率、每花药中花粉粒数均居于其双亲之间,花器官发育及其形态发生具有双亲的特点.但小花粉及花粉母细胞减数分裂过程中形成的不正常四分体比率远远高于其双亲.以体细胞杂种“哈姆林甜橙+粗柠檬”为花粉亲本,与二倍体单胚类型宜昌橙与华农本地早的有性后代杂交,获得了110棵有性后代植株,其中三倍体82棵,二倍体和其它倍性的植株28棵.     

哈姆林甜橙与粗柠檬体细胞杂种的育性

对异源四倍体柑桔体细胞杂种“哈姆林甜橙＋粗柠檬”及其亲本的花粉活力,花器官发育,花器官形态发生与共母细胞减数分裂四分体阶段进行了观测和统计,结果发现：“哈姆林甜橙＋粗柠檬”的花粉染色活力,萌发率,线花药中花粉粒数均居于其双亲之间,花器官发育及其形态发生具有双亲的特点,但小花粉及花粉母细胞减数分裂过程中形成的不正常四分体比率远远高于其双亲。以体细胞杂种“哈姆林甜橙＋粗柠檬”为花粉亲本,与二倍体单胚类型宜昌橙与华农本地早的有性后代杂交,获得了110棵有性后代植株,其中三倍体82棵,二倍体和其它倍性的植株28棵。     

柑橘体细胞杂种有性后代的创造及杂种鉴定

以异源四倍体柑橘体细胞杂种[哈姆林甜橙(Citrus sinensis Osbeck) 粗柠檬(C.jambhiri Luss)]为父本与二倍体单胚类型宜本杂4号[华农本地早橘(C.reticulata Blanco)×宜昌橙(C.ichangen- sis Swingle)]杂交,采用胚抢救技术获得了110株有性后代植株,通过染色体计数及倍性分析仪鉴定,其中93株植株为3倍体,余下的17林植株为2倍体。RAPD分析表明:获得的有性后代植株均为杂种。     

RAPD为基础的柑橘体细胞杂种有性后代遗传研究

筛选31条谱带清晰、多态性强及重复性好的10 bp引物, 运用RAPD技术对以异源四倍体柑橘体细胞杂种(哈姆林甜橙(Citrus sinensis Osbeck)+粗柠檬(C. jambhiri Luss))为父本与二倍体单胚类型宜本杂4号(华农本地早橘(C. reticulataBlanco)×宜昌橙(C. ichangensis Swingle))杂交获得的杂种后代进行遗传分析. χ₂测验表明: 杂交父本与母本的特异标记总体上是随机传递给后代的, 父本即柑橘异源四倍体体细胞杂种融合双亲的单个特异标记也是随机传递给后代的. 通过组群平均数假设测验, 二倍体组群与三倍体组群间各类亲本标记的平均数不存在显著差异. 基于遗传距离的聚类结果显示: 杂种后代聚为3类: 第1类与融合亲本之一哈姆林甜橙聚为一类, 有15株杂种后代; 第2类与母本宜本杂4号聚为一类, 有16株杂种后代; 第3类与父本体细胞杂种(哈姆林甜橙+粗柠檬)聚为一类, 有61株杂种植株, 大多数杂种后代与父本的遗传关系更为密切.     

柑桔细胞电融合再生两个种间体细胞杂种

朋娜脐橙(Citrussinensis Osbeck)胚性细胞悬浮系原生质体分别与粗柠檬(C.jambhiri Lush)、枸头橙(C.aurantium)叶肉原生质体经电场诱导而融合。经培养,两组合均获得再生植株。对朋娜脐橙+粗柠檬的再生胚状体进行染色体计数,随机取样的52个胚状体中,26个为四倍体,另外26个为二倍体;对74棵再生植株进行染色体计数,由此说明都为四倍体;表明体细胞杂种在植株再生过程中具有明显的竞争优势。朋娜脐橙+枸头橙再生的14棵植株都为四倍体。对朋娜脐橙+粗柠檬部分植株进行POX同工酶和RAPD分析,表明所有检测植株都为杂种。朋娜脐橙+枸头橙再生植株经RAPD分析,表明也为杂种。     

原生质体融合获得柑桔种间体细胞杂种

粗柠檬(Citrus jambhiri Lush)叶肉原生质体与哈姆林甜橙(C.sinensis L.Osbeck)胚性悬浮细胞系原生质体经PEG诱导融合,培养7天时原生质体恢复分裂。再生的胚状体在含有GA_3的培养基中萌发出茎芽。茎芽经生根诱导成为完整植株。对首批再生的5棵植株进行染色体检查,结果表明,全为四倍体,2n=4x=36。淀粉胶电泳分析过氧化物酶同工酶,结果显示这5棵植株为体细咆杂种。粗柠檬和哈姆林甜橙在该位点上均为同质结合,基因型分别是MM和FF。体细胞杂种含有双亲的酶带,基因型为MMFF。杂种植株生长旺盛,根系发达,叶片及植株形态介于双亲之间。本文对其作为砧木品种的可能性等问题作了讨论。     

两类柑橘杂种砧木对脐橙幼树生长及若干生理生化指标的影响

以体细胞杂种红橘+枳、红橘+粗柠檬和有性杂种Swingle枳柚、Troyer枳橙(对照)作砧木的脐橙幼树为试材,以盆栽试验研究砧木对幼树的影响。结果表明,体细胞杂种砧木处理和有性杂种Swingle枳柚的树体生长势总体上强于对照;叶片可溶性糖含量较高的是红橘+粗柠檬处理和对照;叶绿素含量最高的是红橘+粗柠檬处理。两年中叶片POD活性分别与当年树冠体积呈负相关。     

甜橙与酸橙体细胞杂种核质组成鉴定(英文)

采用流式细胞术(flow cytometry, FCM)、简单重复序列(simple sequence repeat, SSR)和酶切扩增多型性序列(cleaved amplified polymorphic sequence, CAPS)等技术分析酸橙(Citrus aurantium L. )叶肉原生质体和甜橙(C. sinenis Osbeck cv. Shamouti)胚性愈伤组织原生质体电融合再生的体细胞杂种。FCM研究结果表明,所有的体细胞杂种植株荧光强度是二倍体对照的2倍,说明所分析的植株为四倍体。用SSR和CAPS分析了体细胞杂种的核质遗传组成,在试验的4对SSR引物中,有2对能区分开融合亲本。在2对引物中,体细胞杂种植株包含双亲的全部特异带,表明它们为异核杂种。通用引物扩增结合限制性内切酶酶切能鉴别融合亲本,在具有多型性的引物/酶组合中,所有体细胞杂种的线粒体和叶绿体DNA带型与胚性亲本(甜橙)完全一样。结果表明体细胞杂种核基因组来自双亲,而胞质基因组来自悬浮系亲本。讨论了所用技术的特点、柑橘四倍体体细胞杂种核质遗传规律及本组合体细胞杂种的应用。     

甜橙与酸橙体细胞杂种核质组成鉴定

采用流式细胞术(flow cytometry,FCM)、简单重复序列(simple sequence repeat,SSR)和酶切扩增多型性序列(cleaved amplifiedpolymorphic sequence,CAPS)等技术分析酸橙(Citrus aurantium L.)叶肉原生质体和甜橙(C.sinenis Osbeck cv.Shamouti)胚性愈伤组织原生质体电融合再生的体细胞杂种.FCM研究结果表明,所有的体细胞杂种植株荧光强度是二倍体对照的2倍,说明所分析的植株为四倍体.用SSR和CAPS分析了体细胞杂种的核质遗传组成,在试验的4对SSR引物中,有2对能区分开融合亲本.在2对引物中,体细胞杂种植株包含双亲的全部特异带,表明它们为异核杂种.通用引物扩增结合限制性内切酶酶切能鉴别融合亲本,在具有多型性的引物/酶组合中,所有体细胞杂种的线粒体和叶绿体DNA带型与胚性亲本(甜橙)完全一样.结果表明体细胞杂种核基因组来自双亲,而胞质基因组来自悬浮系亲本.讨论了所用技术的特点、柑橘四倍体体细胞杂种核质遗传规律及本组合体细胞杂种的应用.     

Extensive citrus triploid hybrid production by 2x?×?4x sexual hybridizations and parent-effect on the length of the juvenile phase

The citrus fresh market demands the production of seedless citrus fruits, as seedy fruits are not accepted by consumers. The recovery of triploid plants has proven to be the most promising approach to achieve this goal, since triploids have very low fertility, are generally seedless and do not induce seeds in other cultivars by cross pollination. Triploid plants can be recovered by 2x?×?4x sexual hybridization. In this work, we present an effective methodology to recover triploid plants from 2x?×?4x hybridizations based on in vitro embryo rescue, ploidy level analysis by flow cytometry and genetic origin of triploid plants. The pollen viability of diploid and tetraploid citrus genotypes was analyzed by comparing the pollen germination rate in vitro. The pollen viability of tetraploid (doubled-diploid) genotypes is generally reduced but sufficient for successful pollination. Triploid embryos were identified in normal and undeveloped seeds that did not germinate under greenhouse conditions. The influence of parents and environmental conditions on obtaining triploid plants was analyzed and a strong interaction was noted between the parents and environmental conditions. The parental effect on the length of the juvenile phase was also demonstrated through observations of a large number of progeny over the last 15?years. The juvenile phase length of the triploid hybrids obtained with 'Fortune' mandarin as female parent and tetraploid 'Orlando' tangelo as male parent was shorter than the juvenile phase obtained with a clementine as female parent and tetraploids of 'Nova', 'W. Leaf' and 'Pineapple' male parents. Key message Effective methodology to recover citrus triploid plants from 2x?×?4x sexual hybridizations and the parental effect on the length of the juvenile phase.     

Citrus tissue culture employing vegetative explants

Citrus being a number one fruit of the world due to its high nutritional value, huge production of fruits and fruit products, the citrus industry may be considered a major fruit industry. Though citrus orchard area in India is comparable to USA, the produce is far less, while its export is nil. Biotechnology has played an outstanding role in boosting the citrus industry, e.g., in Spain, which is now the biggest exporter of citrus fruit with the application of micrografting. Amongst the fruit trees, perhaps the maximum tissue culture research has been done in citrus during the past four decades, however, the results of practical value are meagre. The shortfalls in citrus tissue culture research and some advancements made in this direction along with bright prospects are highlighted, restricting the review to vegetative explants only. Whilst utilization of nucellar embryogenesis is limited to rootstocks, the other aspects, like, regeneration and proliferation of shoot meristems measuring 200 microm in length--a global breakthrough--of two commercially important scion species, Citrus aurantifolia and C. sinensis and an important rootstock, C. limonia, improvement of micrografting technique, cloning of the same two scion species as well as some Indian rootstock species, employing nodal stem segments of mature trees, of immense practical value have been elaborated. A rare phenomenon of shift in the morphogenetic pattern of differentiation from shoot bud differentiation to embryoid formation occurred during the long-term culture of stem callus of C. grandis. Stem callus-regenerated plants of C. aurantifolia, C. sinensis and C. grandis showed variation in their ploidy levels and a somaclonal variant of C. sinensis, which produced seedless fruits was isolated. Tailoring of rooting in microshoots to a tap root-like system by changing the inorganic salt composition of the rooting medium, resulting in 100% transplant success, and germplasm preservation through normal growth culture of shoots of C grandis without loss of regeneration capacity during 31 years, observed so far, are some other significant results. Plants of C. aurantifolia and C. sinensis raised from shoot meristem and micrografting were grown in a nethouse and those from nodal stem segments in the field along with the in vitro-raised plants of rootstocks, namely, C. jambhiri, C. karna and C. limonia. All the plants showed normal healthy growth. Significantly enough, the meristem regenerated plants of C. aurantifolia attained the reproductive phase just in 1 year of transplantation to soil similar to those raised from nodal stem segments of mature trees, which also produced normal fruits in the subsequent year while growing under field conditions. Thus, a significant fundamental concept of a maturity factor, carried over through as small a shoot meristem as 200 microm in length to cloned plants has been demonstrated. The concept is of far-reaching significance in citrus industry besides production of pathogen-free orchards.     

强德勒红心柚离体培养与植株再生体系的建立

以强德勒红心柚（Citrus grandis Osbeckcv. Chandler）种子萌发的无菌苗为材料,选取子叶、子叶节段、上胚轴、带芽的茎段进行离体培养研究。结果表明：子叶节段是诱导丛生芽的最佳外植体,诱导率100%;诱导丛生芽的最佳培养基为MS＋6-BA2.0mg/L＋NAA0.05mg/L＋蔗糖30g/L＋活性炭0.4g/L,丛生芽增殖可达11.2倍;最适生根培养基为1/2MS＋NAA0.5mg/L,生根率达100%,移栽15d后成活率100%。     

柑橘大实蝇对不同柑橘品种的产卵偏好和幼虫取食选择

【目的】掌握柑橘大实蝇Bactrocera minax对不同品种柑橘的产卵偏好,以及与幼虫取食喜嗜性的关系。【方法】我们用五点取样法分别调查了自然条件下不同品种柑橘果园的虫果率,统计了各品种柑橘虫果基半部和端半部产卵痕量和卵量,并在实验室内采用培养皿桔瓣选择法研究了其幼虫对不同柑橘品种果实的取食选择。【结果】在未采取防控措施的情况下,果树面朝杂树林的方位虫果率显著高于其他方位;同一片受害柑橘园内,不同柑橘品种的虫果率为脐橙Citrus sinensis cv. Navel、酸橙C. aurantium＞冰糖橙C. sinensis cv. Bingtang、天草(Amakusa)、蜜橘C. reticulata cv. Satsuma＞沙田柚C. maxima cv. Shatian＞椪柑C. reticulata cv. Ponkan;柑橘大实蝇产卵痕数和卵量均为橙类（脐橙、酸橙和冰糖橙）大于橘类（天草、蜜橘和椪柑）和沙田柚（P＜0.05）;除蜜橘外,所调查的其他柑橘品种端半部的产卵痕数显著多于基半部（P＜0.05）;幼虫对不同品种柑橘橘瓣肉的取食选择顺序依次为：脐橙、酸橙＞冰糖橙＞天草、南橘C. reticulata cv. Nanju＞蜜橘＞椪柑＞沙田柚。【结论】结果提示,柑橘大实蝇成虫偏向于选择幼虫所喜嗜的橙类品种产卵,且产卵量更多。     

杂交柑桔的胚胎发育(英文)

柑桔类珠心胚现象对研究其进化和种质保存方面有着重要意义,但是给其有性杂交育种工作造成相当大的麻烦：它不仅使杂交后代难于区分合子苗和珠心苗,而且会使合子胚发育中途天折。解决的途径是适时分离合子胚进行单独培养。为此,本工作于柑桔胚胎发育的不同时期取样、固定、观察,研究其合子胚发育规律,确定珠心胚侵入胚囊的时期。结果表明：一般情况下,授粉后３０ｄ,合于处于单细胞状态（Ｆｉｇ．１Ａ）;授粉后４０ｄ;合子开始分裂（Ｆｉｇ．１Ｂ）;授粉后４５ｄ,合子胚形成８－１６个细胞,珠心胚开始分裂（Ｆｉｇ．１Ｃ）;授粉后５０ｄ,合子形成球形胚,珠心胚尚未侵入胚囊（Ｆｉｇ．１Ｄ＆Ｅ）;授粉后５５ｄ,合子胚为球形胚或早心形胚,开始有少数珠心胚侵入胚囊（Ｆｉｇ．１Ｄ＆Ｅ）;授粉后６０ｄ,合子胚为心形胚（Ｆｉｇ．１Ｇ）。授粉后８０ｄ,合子胚为晚心形,珠心胚巨大量侵入并迅速发育（Ｆｉｇ．１Ｈ）。杂交的组合对合子,胚珠及果实发育均有一定影响,主要取决于杂交亲本。与种间杂交相比,属间杂交其合子分裂较迟,合子胚发育较慢,珠心胚侵入时期也较迟（Ｔａｂｌｅｌ,Ｆｉｇ．２）。这种发育速度的差异,引起所产生的合子胚的大小（Ｔａｂｌｅ２）珠心胚侵率（Ｔａｂ     

抗根肿病大白菜的花药培养

大白菜是中国北方的重要蔬菜之一,根肿病是危害大白菜生产世界性病害,利用花药培养可以大大加速抗根肿病大白菜杂交育种工作的进程。对33份抗根肿病大白菜品种(品系)进行花药培养,有24个品种诱导出胚,品种诱导率为72.7%,以东方皇冠×C11的诱导率最高,为1.86胚/蕾。对大部分基因型来说,在培养基中添加0.4 g/L谷氨酰胺的诱导效果最好。研究还发现生长在温室中的供体植株更容易诱导出胚状体。变绿的子叶型胚转到B5+0.2 mg/L BA+0.1 mg/L NAA+0.1%活性炭的胚分化培养基上可诱导生芽。     

节节麦×普通小麦杂种的胚援救和胚愈伤组织再生植株

通过活体-离体胚培养和胚愈伤组织培养有效地克服了节节麦(Aegilops tauschii Cosson.)×小麦(Triticum aestivum L.)杂种幼胚的败育,产生了大量的杂种植株。采用活体-离体胚培技术,节节麦×小麦三个组合杂种幼胚的成苗率为55%,是前人所用传统胚培方法成功率的5—20倍。杂种幼胚在添加有2 mg/L 2,4-D的MS培养基上诱导为愈伤组织,经继代产生全能性愈伤组织,继而分化出再生植株。愈伤组织经继代保存150天仍不丧失分化能力。本文还对两种产生杂种的组织培养方法进行了比较研究。     

Establishment of a System with High Synchronous Frequency of Somatic Embryogenesis and Embryo Seedling Formation in Camellia sinensis var. assamica

The system of high synchronous frequency of somatic embryogenesis and somatic embryo seedling formation was established by means of embryonic cell hne 1 ( CL1 ) of Camellia sinensis var. assamica Kitamura. Modified MS was used as the basic medium. Cultures of CL1 was transferred to the aqueous induced medium (0.05 mg/L 2,4-D + 0.50 mg/L 6-BA) from the maintenance medium (0.1 mg/L 2,4-D + 0.5 mg/L 6-BA) for somatic embryos induction under dark condition. 28 days later, they were cultured in the liquid differentiation medium. Various kinds of somatic embryos were obtained after another 28 days. The frequency of somatic embryos was 81.5 %. Various mesh sizes of sieves were applied to collect the somatic embryos in different developmental stages which could develop to mature stage in the aqueous growth medium ( 1/2 MS + 1.0 mg/L GA3 + 0.5 mg/L 6-BA). ABA was effective to promote the formation of highly qualified somatic embryo. The mature somatic embryos sized 20 to 70 mesh had the conversion frequency 75 %. The development of somatic embryogenesis studied under a cell suspension culture system was similar to the zygotic embryogenesis.     

Implementation of extensive citrus triploid breeding programs based on 4x?×?2x sexual hybridisations

Seedlessness is one of the most important characteristics for mandarins for the fresh-fruit market, and mandarin triploid hybrids have this trait. Triploid citrus plants can be recovered by 4x?×?2x hybridisations using non-apomictic genotypes as female parents. In this study, we characterise the type of seeds obtained in 4x?×?2x hybridisations and the ploidy level of plants recovered from each type of seed. The majority of the plants recover were triploid (98.3?%), but a few diploid, tetraploid and pentaploid plants were also produced and their genetic origin was analysed by simple sequence repeat (SSR) markers. We also analysed the influence of parents and environmental conditions on the efficiency of recovery triploid hybrids. In this work, we present an effective methodology to recover triploid hybrids from 4x?×?2x hybridisations based on in vitro embryo rescue and determination of ploidy level by flow cytometry that allow us to recover more than 4,400 triploid hybrids from more than 60 parental combinations.