Callus conclusion

For some years students of science and industry have been predicting the pervasive impact of biotechnology on the health care industry. Much has been discussed about the role biotechnology will play in industrial process, diagnostics, and pharmaceutical products. This review examines two branches of biotechnology which are emerging in the in-vitro diagnostics arena which are likely to bear edible fruit in the current decade—monoclonal antibodies and DNA probes.     

杂景天愈伤组织诱导及红景天苷测定

以杂景天的子叶、胚轴为外植体,接种在附加不同激素组合的MS培养基上诱导愈伤组织产生,愈伤组织经继代培养后,用高效液相色谱检测红景天苷含量.结果显示,杂景天的子叶是诱导愈伤组织的理想外植体,子叶在MS 1 mg/L BA 0.5 mg/L 2,4-D和MS 1 mg/L BA 0.5 mg/L NAA培养基上的愈伤组织诱导率较高(81.8%、80%).愈伤组织有红、绿2种类型.HPLC检测显示红色愈伤组织不含红景天苷,绿色愈伤组织红景天苷含量为0.288 6%.表明利用组织培养生产红景天苷是可行的.     

石蒜愈伤组织的诱导及其继代培养

以石蒜鳞茎为外植体,研究了不同激素组合、鳞茎不同部位和不同生长时期等因素对石蒜愈伤组织诱导的影响及其继代培养。结果表明：MS＋2,4-D 1 mg·L~（-1）＋6-BA 1 mg·L~（-1）激素组合能较好的诱导出石蒜愈伤组织,诱导率达61.13%;外植体的选择是石蒜愈伤组织诱导的关键因素,内层鳞茎诱导愈伤组织的效果最好;在一个生长周期中,9、10月的鳞茎作为外植体诱导愈伤组织最佳;MS＋2,4-D 0.5 mg·L~（-1）＋KT 0.5 mg·L~（-1）是愈伤组织较好的继代培养基,继代周期为24～27 d。     

抗生素对大豆愈伤组织的诱导和生长的影响

用红霉素、头孢唑啉钠、头孢拉定、头孢霉素(国产和进口)等5种抗生素对农杆菌LBA4404进行抑菌试验,以头孢霉素的抑菌效果最好.头孢霉素作为抑菌剂用于大豆遗传转化试验时,在下胚轴浓度以300mg/L,在子叶节以500mg/L为宜.大豆品种对卡那霉素的反应在出愈率上表现相似,在褐化率上表现有些不同.大豆不同外植体对卡那霉素的反应存在较大差异,以真叶反应最敏感,下胚轴反应最迟钝.在以卡那霉素作为抗性选择标记时,选择压力真叶和子叶节以50～100mg,L为好,下胚轴以100～200mg/L为宜。 Ahstract:The experiment of inhibiting Agrobacterium LBA4404 was undertaken with 5 antibiotics (the Erythronycin Base,Cefazolin Sodium,Cefradine,2 kinds of Cefotaximes).Among them,Cefotaxime showed the best effect.When Cefotaxime is used in transformation,the ideal concentration is 300mg/L in hypocotyl and 500mg/L in cotyledon node.The response of soybean varieties to Kanamycin is similar in induction of callus rate and is different in brown rate of callus.Differences of the response of soybean explants to Kanamycin were found.The young leaves are sensitive to Kanamycin,but hypoeotyl is not.The ideal selecting pressure of Kanamycin is 50- l00mg/L in young leaf and cotyledon node,andl00-200mg/L in hypocotyl when Kanamycin is used as selection marker.     

抗生素对大豆愈伤组织的诱导和生长的影响

用红霉素、头孢唑唑钠、头孢拉定、头孢霉素（国产和进口）等5种抗生素对农杆菌LBA4404进行抑菌试验,以头孢霉素的抑菌效果最好。头孢霉素作为抑菌剂用大于豆遗传转化试验时,在下胚轴浓度以300mg/L,在子叶节以500mg/L。大豆品种对卡那霉素的反应在出愈率上表现相似,在褐化率上表现有些不同。大豆不同外植体对卡那霉素的反应存在较大差异,以真叶反应最敏感,下胚轴反应最迟钝。在以卡那霉素作为抗性选择标记时,选择压力真叶和子叶节以50－100mg/L为好,下胚轴以100－200mg/L为宜。     

蝴蝶兰愈伤组织诱导研究

对蝴蝶兰愈伤组织诱导试验结果表明,授粉后30d的蝴蝶兰子房适宜诱导愈伤组织,在1/4MS+2,4-D1.0mg/L+6-BA 0.1mg/L+蔗糖3.0%培养基上,蝴蝶兰子房切段愈伤组织的诱导率达到90.0%。     

Callus stimulation in distraction osteogenesis

Distraction osteogenesis has been described as in vivo tissue engineering. The ability to stimulate this process for the repair of bony defects or lengthening of congenitally shortened facial structures is likely to significantly impact the field of craniofacial surgery. The purpose of this study was to determine whether mechanical stimulation of the distracted rabbit mandible would accelerate the maturation of the bony callus when applied during the early consolidation period. Twenty adult New Zealand White rabbits underwent unilateral mandibular osteotomy. A uni-directional internal distractor device (Synthes, Paoli, Pa.) was positioned along a plane perpendicular to the line of osteotomy. After a 7-day latency period, distraction was commenced at a rate of 1.0 mm/day for 12 days in all animals. In a control group of 10 rabbits, a consolidation period of 8 weeks was observed before they were killed. In the experimental group of 10 rabbits, daily alternate compression and distraction of 1 mm (sequential compression and distraction) was performed for 3 weeks followed by a 5-week period of rigid fixation. Each animal received a dose of a fluorescent label at three different time points during the study: at the end of the distraction period, 3 weeks after the completion of the distraction phase, and 3 days before it was killed. All animals were killed 8 weeks after the completion of the distraction phase. Undecalcified histologic analysis and 3-point bending tests to failure were performed on the extracted mandibles. The results of the experimental and control groups were compared.Four animals in the control group and three animals in the experimental group were excluded from the study because of screw loosening resulting in distractor dislodgment or because of infection. On histologic analysis, cortical thickness at the center of the callus was found to be significantly greater in the experimental group compared with the control group when normalized to the contralateral hemimandible (83 percent versus 49 percent, respectively; p < 0.007). The ratio of cortical to cancellous bone in the distracted callus was uniformly found to be greater in the experimental specimens. The mineral apposition rate was calculated by using fluorescence microscopy and found to be significantly greater in the experimental group both during the period of sequential compression and distraction (3.2 microm/day versus 2.1 microm/day, p = 0.02) and after the period of sequential compression and distraction (1.4 microm/day versus 1.1 microm/day, p = 0.006). Mechanical testing revealed no significant differences in bending strength or stiffness between experimental or control groups (p = 0.54 and 0.47, respectively). This study has demonstrated that daily alternating compression and distraction of 1 mm amplitude during the early consolidation period has a stimulatory impact on callus formation with respect to osteoblastic activity, remodeling, and maturation of bone. Optimal timing and amplitude of sequential movement, long-term biomechanical differences, and molecular pathways have yet to be elucidated.     

细毛樟愈伤组织培养

从富含香叶醇的细毛樟（ＣｉｎｎａｍｏｍｕｍｔｅｎｕｉｐｉｌｕｍＫｏｓｔｅｒｍ）叶片外植体诱导出愈伤组织。愈伤组织生长较合适的培养基为ｐＨ５．８附加ＩＡＡ２ｍｇ／Ｌ和ＫＴ０１ｍｇ／Ｌ的ＭＳ培养基,在２５℃下暗培养。愈伤组织无性系继代培养到第６代后芳香成分初步分析结果表明主成分仍为香叶醇。     

苜蓿愈伤组织中的盐胁迫蛋白

0.5％NaCl抑制愈伤组织生长,处理后期(第21天和28天检测)24kD蛋白含量明显增加。1.0％,2.0％和3.0％NaCl处理的愈伤组织不生长,未检出24kD蛋白增加,但36～42kD蛋白大量增加,并且有随处理的盐浓度增高而增加的趋势。 在1.0％NaCl适应愈伤组织(简称S-1)中24kD蛋白含量明显增加,而36～42 kD蛋白含量下降到对照水平。~(35)S-Met体内标记表明,增加的24kD蛋白是新合成的。S-1回到无盐5代后,仍保持提高的耐盐性和24kD蛋白含量。24kD蛋白含量的增加不受甘露醇胁迫的诱导。初步离心分离的细胞亚组分表明,24kD蛋白主要位于胞质和细胞器膜。在烟草S-1细胞中也发现24kD蛋白含量增加。     

茶条槭愈伤组织的再生体系建立及其没食子酸含量的测定

通过愈伤组织诱导途径, 建立了快速高效的茶条槭再生体系。成熟种子在MS+1.0 mg·L-1 6-BA的培养基中萌发, 以茎段作为外植体, 在WPM+0.002-0.01 mg·L-1 TDZ+0.1 mg·L-1 6-BA中培养3周诱导形成愈伤组织, 诱导频率平均为98.0%。愈伤组织转入WPM+0.01 mg·L-1 TDZ+0.1 mg·L-1 6-BA培养基中得到再生芽, 分化频率为42.0%,平均每块愈伤产生再生芽10个左右。转到WPM+0.3 mg·L-1 IBA的培养基上的再生芽均可生根并长成完整植株, 小苗移栽成活率达到89.0%。实验还建立了愈伤组织中没食子酸的提取和HPLC检测方法。对深绿色愈伤组织连续培养2个继代后, 没食子酸含量达到2.8%。     

Caffeine Formation in Tea Callus Tissue

Callus tissue derived from segments of the stems of the teaplant produced caffeine. The caffeine was found in the tissueand was also present in the growth medium. The amount of caffeinevaried with the duration and conditions of growth of the callus.Theobromine was also produced by the callus. The methylatedpurines appeared during the latter half of the period of therapid phase of growth. It is probable that the caffeine wasformed by those cells nearing the end of growth, maybe whenthe cells were autolysing. Suspensions of cells which were mechanicallybroken in a phosphate buffer at pH 7.2 produced more caffeineduring incubation at 26 ?C. If the autolysates were supplementedwith RNA and methionine the amount of caffeine produced couldbe increased. It is suggested that the caffeine is formed duringthe catabolic breakdown of nucleic acids rather than directlyfrom the pathways of purine synthesis.     

Cytology of Callus of Cryptomeria japonica

Callusing has been initiated from the cotyledons of 4-week-old seedlings of Cryptomeria japonica on Murashige and Skoog's medium supplemented with 22.8 μM IAA. Callus was grown successfully for more than 2 years on the same medium without any decline in growth vigour. The callus has shown differentiation of tracheids with reticulate thickenings but differentiation of root, shoot or whole plant has not yet been observed. Cytology of 2-month-old callus showed the presence of cells containing normal diploid chromosome complement of 2n = 22 and normal mitosis. However, the 6-month-old callus revealed majority of cells with normal diploid complement and the usual karyotype, but a few cells were noticed with aneuploid numbers ranging from 2n = 15–17. Anaphase bridges and lagging chromosomes have also been encountered.     

Starch Metabolism in Shoot-forming Tobacco Callus

Starch, free sugars and protein contents, and the specific activitiesof enzymes of starch metabolism were determined in tobacco calluscultured under shoot-forming and non-shoot-forming conditions.Shoot-forming cultures contained higher levels of starch, freesugars and protein. Shoot-forming cultures had higher specificactivities for starch-synthesising enzymes throughout culture.On the other hand, higher levels of activity for starch-degradingenzymes in shoot-forming tissues were only observed during organizeddevelopment. The role of phosphorylase in the cultured tissuewas not clear.     

黄芩愈伤组织诱导研究(简报)

以黄芩带节茎段为外植体,在含6-BA1．0mg／L和NAA0．2mg／L的MS培养基上培养,可直接分化出芽,分化芽的茎段在相同培养基及培养条件下能够诱导形成愈伤组织。     

Wheat Callus Culture: the Initiation, Growth and Organogenesis of Callus Derived from Various Explant Sources

Callus was obtained from mature excised embryos of wheat, fromnodal and internodal stem segments and from rachis segmentsusing the medium of Murashige and Skoog(1962)(M medium), containing1-0mg l^–1 2,4-D, and from immature embryos using the mediumof Green and Phillips (1975) containing 2 mg l^–1 2,4-D.Callus yield from mature embryos depended upon the cultivarused. No callus could be obtained from leaf segments. Callusderived from mature embryos and nodal stem segments was successfullymaintained by serial sub-culture on the M medium containing2,4-D for up to 3 years although its growth rate declined toa lower level as culture proceeded. Such cultures consistently produced roots when transferred toa medium containing a low level of 2,4-D or no 2,4-D. The presenceof the auxin was essential for continued proliferation of thecallus tissue. Shoot initiation was infrequent, did not occurafter the first few sub-cultures and could not be enhanced byvarious auxin and cytokinin additions to the medium. Callusderived from immature embryos did not have an enhanced potentialfor shoot initiation. Triticum aestivum, wheat, callus culture, organogenesis     

Studies on Initiation of Apple Endosperm Callus and Variations of Chromosomal Ploidy on Callus Cells of Endosperm

The present paper deals with the initiation of endosperm callus of apple and the ploidy on callus cells through subcultures. According to our observations, the low capacity of differentiation has been discussed. The following conclusions are drawn: 1. The callus initiaed at 2–5 layer cells beneath epidermis. Some cells in this region changed into initials of endosperm callus and from initial masses then develop into cellular masses of endosperm callus protruding on the endosperm surface. The differentiation and growth of callus masses through subcultures may carry out in embryonal and transitional cellular masses in the peripheral zone and basal zone. 2. The ploidy in callus cells is very unstable. Through repeated subcultures the ploidy of the callus cells vary greatly. Most cells (about 80%) contain polyploid and a large number of aneuploid neuclei, while the triploid cells only constitute the minority (about 2.5%–3%). Hence the ploidy in callus cells produced by well developed endosperm vary greatly. 3. It is highly probable that the above mentioned variation of ploidy in callus cells of endosperm, particularly within the embryonal and transitional cellular masses is the cause of the low capacity of differentiation.     

茶条槭愈伤组织的再生体系建立及其没食子酸含量的测定

通过愈伤组织诱导途径,建立了快速高效的茶条槭再生体系。成熟种子在MS＋1．0mg·L^-1 6-BA的培养基中萌发,以茎段作为外植体,在WPM＋0．002-0．01mg·L^-1 TDZ＋0．1mg·L^-1 6-BAR培养3周诱导形成愈伤组织,诱导频率平均为98．0％。愈伤组织转入WPM＋0．01mg·L^-1 TDZ＋0．1mg·L-^1 6-BA培养基中得到再生芽,分化频率为42．0％,平均每块愈伤产生再生芽10个左右。转到WPM＋0．3mg·L^-1 IBA的培养基上的再生芽均可生根并长成完整植株,小苗移栽成活率达到89．0％。实验还建立了愈伤组织中没食子酸的提取和HPLC检测方法。对深绿色愈伤组织连续培养2个继代后,没食子酸含量达到2．8％。