江苏农业学报
江囌農業學報
강소농업학보
JIANGSU JOURNAL OF AGRICULTURAL SCIENCES
2009年
6期
1330-1334
,共5页
孙少霞%戈伟%王述彬%刘金兵%潘宝贵%刁卫平
孫少霞%戈偉%王述彬%劉金兵%潘寶貴%刁衛平
손소하%과위%왕술빈%류금병%반보귀%조위평
甜(辣)椒%花药培养%胚状体%植株再生
甜(辣)椒%花藥培養%胚狀體%植株再生
첨(랄)초%화약배양%배상체%식주재생
pepper(Capsicum annuum L.)%an-ther culture%embryoid%plant regeneration
以10份不同基因型甜(辣)椒为试材进行花药培养,通过对基因型、取蕾时期、低温预处理、热激处理、碳源及外源激素浓度配比等因素的研究,建立有效的甜(辣)椒花药培养胚状体发生体系.结果表明:基因型是限制甜(辣)椒花药培养胚状体诱导的关键因素,不同品种间出胚率差异显著,其中品种003出胚率最高,为10.8%;处于盛花期的花蕾最适于甜(辣)椒花药培养;4℃低温预处理1-3 d有利于胚状体的诱导,以处理2 d的胚状体产率最高;以2%的麦芽糖代替3%的蔗糖能显著提高出胚率和子叶形胚的比率,筛选出适于甜(辣)椒花药培养胚状体诱导的最佳培养基为Ms+0.5 mg/L NAA+1.0 mg/L KT+2%麦芽糖,能有效地提高出胚率并促进植株冉牛;获得了6个基因型的子叶形胚和再生植株.
以10份不同基因型甜(辣)椒為試材進行花藥培養,通過對基因型、取蕾時期、低溫預處理、熱激處理、碳源及外源激素濃度配比等因素的研究,建立有效的甜(辣)椒花藥培養胚狀體髮生體繫.結果錶明:基因型是限製甜(辣)椒花藥培養胚狀體誘導的關鍵因素,不同品種間齣胚率差異顯著,其中品種003齣胚率最高,為10.8%;處于盛花期的花蕾最適于甜(辣)椒花藥培養;4℃低溫預處理1-3 d有利于胚狀體的誘導,以處理2 d的胚狀體產率最高;以2%的麥芽糖代替3%的蔗糖能顯著提高齣胚率和子葉形胚的比率,篩選齣適于甜(辣)椒花藥培養胚狀體誘導的最佳培養基為Ms+0.5 mg/L NAA+1.0 mg/L KT+2%麥芽糖,能有效地提高齣胚率併促進植株冉牛;穫得瞭6箇基因型的子葉形胚和再生植株.
이10빈불동기인형첨(랄)초위시재진행화약배양,통과대기인형、취뢰시기、저온예처리、열격처리、탄원급외원격소농도배비등인소적연구,건립유효적첨(랄)초화약배양배상체발생체계.결과표명:기인형시한제첨(랄)초화약배양배상체유도적관건인소,불동품충간출배솔차이현저,기중품충003출배솔최고,위10.8%;처우성화기적화뢰최괄우첨(랄)초화약배양;4℃저온예처리1-3 d유리우배상체적유도,이처리2 d적배상체산솔최고;이2%적맥아당대체3%적자당능현저제고출배솔화자협형배적비솔,사선출괄우첨(랄)초화약배양배상체유도적최가배양기위Ms+0.5 mg/L NAA+1.0 mg/L KT+2%맥아당,능유효지제고출배솔병촉진식주염우;획득료6개기인형적자협형배화재생식주.
Ten varieties of pepper were used to study the effects of genotype,flower buds harvest time,cold-pretreat-ment,hot-shock treatment,carbon source and combination of hormones on the anther culture in Capsicum annuum L.Through these tests,an effective system of embryoid production was established.Cotyledonary embryoids and plantlets were obtained from six genotypes.The results showed that genotype was the key factor in embryoid induction.The embryoid for-mation frequency Was different significantly among different genotypes.The variety 003 had the highest embryoid formation frequency which was 10.8%.The flower buds at full-bloom stage were found to optimum for anther culture in pepper.Cold-pretreatment (4℃)for 1-3 d also promoted embryoid induction,while the highest embryoid formation frequency was ob-mined from anther pretreated at 4℃ for 2 d.Embryoid and cotyledonary embryoid formation frequency could be more re-markably improved by 2% maltose than 3% sucrose.The optimal culture medium which could effectively improve embryoid and regenerated plantlets formation Was MS+0.5 mg/L NAA+1.0 mg/L KT+2% maltose.