从环境中分离培养微生物:培养基营养水平至关重要

根据目前的微生物学知识体系,利用现有的微生物培养技术仅仅能够分离和培养部分微生物,自然环境中绝大多数微生物暂不能培养。本文总结归纳了部分微生物培养技术和培养策略,包括采取生境隔离、延长培养时间以及模拟自然环境条件等方法,尤其是培养基的营养水平对可培养微生物数量及种类产生重要影响。简要总结了寡营养微生物及其生态意义,以及营养物浓度影响微生物生长的机理。提出可根据微生物的生态环境条件及细胞生理特性,设计合理的培养条件和培养方法,以及采用多种分离培养方法联合,以期最终提高环境微生物的可培养性。     

未培养微生物研究策略概述

基于未培养微生物数量巨大、种类繁多、基因资源丰富等特点。扼要介绍了未培养微生物的纯培养分离策略和分子生物学研究方法。随着新型培养策略如原位仿生境培养、限制性培养、单细胞微操作等的出现,使未培养微生物的纯培养成为可能。同时由于宏基因组学和高通量DNA测序等现代分子生物学方法技术的逐渐成熟,使来源于未培养微生物的新基因和新活性物质的分离筛选出现了新的机遇与挑战。     

杂交瘤细胞的大量培养

杂交瘤细胞的大量培养是一项迅速发展的技术。本文评述了杂交瘤细胞培养条件和代谢调控方面的研究进展,包括反应器培养中的过程参数优化、细胞损伤和保护、营养物质利用和有害副产物的形成、细胞生长和单抗分泌的动力学以及长期培养的稳定性等问题。同时,本文也讨论了在生物反应器中培养杂交瘤细胞和操作模式和控制策略的研究工作,特别是近年来备受重视的灌注培养和补料培养。     

微生物可培养性低的生态学释因与对策

纯培养技术一直是微生物学研究的基石,但其单一的营养结构和生境与自然环境中微生物多样性、协同代谢等明显矛盾,从而成为部分微生物难以复苏的主要障碍。细菌共同协作的自然生存方式的崩溃、生境的极度营养变化和生态位巨变等是微生物可培养性低的主要生态学原因。非培养技术、加富培养、混合培养、稀释培养、模拟自然培养和综合方法等是主要的研究手段和策略,可在不同程度上解决微生物可培养性低的缺陷和问题。     

杂交瘤细胞的大量培养

杂交瘤细胞的大量培养是一项迅速发展的技术。本文评述了杂交瘤细胞培养条件和代谢调控方面的研究进展,包括反应器培养中的过程参数优化、细胞损伤和保护、营养物质利用和有害副产物的形成、细胞生长和单抗分泌的动力学以及长期培养的稳定性等问题。同时,本文也讨论了在生物反应器中培养杂交瘤细胞的操作模式和控制策略的研究工作,特别是近年来备受重视的灌注培养和补料培养。     

李组织培养研究进展(综述)

本文介绍李茎尖培养、茎段培养、胚培养、原生质体培养及叶片培养,分析其中的有关影响因子,重点阐述不同碳源和外源附加物对试管苗生长和分化的影响,并提出李组织培养的存在问题及解决途径。     

液体或固体培养对环链棒束孢(Isaria cateinannulata)菌丝体中挥发性成分组成的影响

[目的]测定环链棒束孢(Isaria cateinannulata)在不同培养方式下,其菌丝中挥发性代谢物组成,分析代谢产物差异与培养方式间的相互联系.[方法]分别用SDAY培养基固体平板与SDY培养基液体摇瓶的培养方式进行培养;培养温度为25℃,培养周期为8天;用同时蒸馏萃取装置提取菌丝的挥发性成分;用气质联用仪进行数据采集及分析.[结果]固体培养菌丝体含有较多种类的挥发性成分,共鉴定41种化合物,其中酯类、醌类和肟类化合物为其特有.液体培养菌丝体含有的挥发性成分相对较少,共鉴定32种化合物,其中羧酸类化合物为其特有,同时酚类含量远高于固体菌丝.固体和液体培养菌丝体的主要挥发性成分都是烃类物质,其中烯烃类物质分别占固体培养菌丝和液体培养菌丝总挥发物的57.6％和7.85％,烷烃类物质分别占固体培养菌丝和液体培养菌丝总挥发物的9.19％和22.4％.[结论]固体或液体培养条件对环链棒束孢菌丝体中挥发性成分的组成有影响.     

牛体外受精卵在两种共同培养系统中发育的研究

为了使牛体外受精卵能通过体外早期发育阻滞期,我们建立了卵丘细胞单层(A)和输卵管上皮单层(B)两种共同培养系统。A1共同培养实验是在本实验室进行的,A2和B共同培养实验均在日本岗山大学农学部动物繁殖学研究室进行,牛输卵管组织的分离使用0.76％EDTA—PBS溶液,共同培养系统均使用含10％小牛血清的TCM—199(Earle's salts)作为培养液。培养的卵泡卵母细胞体外成熟率为100％,体外受精率为99—100％。在A1共同培养实验中,越过阻滞期发育到16—细胞以上的胚胎占卵裂胚的35.7％,与A2共同培养实验中越过阻滞期的发育率(40.1％)无显著差异(P<0.05)。A1和A2共同培养实验,在卵裂基础上得到的桑椹胚和囊胚发育率分别为23.7％和27.9％。每百枚培养的卵母细胞,在A1共同培养实验中可获得桑椹胚和囊胚15.1枚,在A2共同培养实验中可获桑椹胚和囊胚的20.5枚。B共同培养实验中桑椹胚和囊胚发育率为54.1％,显著高于A1或A2共同培养实验的相应发育率(P<0.001),使用B共同培养系统每百枚培养的卵母细胞可以获得37枚桑椹胚和囊胚。     

大豆根瘤菌与磷细菌混合培养下的互作效应

对研究室保藏、无拮抗作用的菌种大豆根瘤菌R12和磷细菌S7进行不同的培养处理,根据生物量及解磷量的变化,探讨二者间相互作用的效应。试验共设5个处理:R12单独培养,S7单独培养,(R12+S7)混合培养,(R12+S7单独培养后的除菌上清液)混合培养,(S7+R12单独培养后的除菌上清液)混合培养,定期测定活菌数和解磷量,结果表明,R12和S7对彼此的生长有不同的促进作用,混合培养下R12为优势菌株活菌数增加明显,S7的活菌数增长幅度较小,但对S7解磷量,混合培养和加R12单独培养后的除菌上清液较S7单独培养高出23.6%和27.8%,由此推测S7单菌解磷能力有所提高。     

环境微生物培养新技术的研究进展

遍布于地球上各种生境中的微生物具有丰富的物种多样性.迄今为止,能够在实验室条件下培养的微生物仅仅是其中的一小部分,微生物物种的绝大多数还都难以在现有培养技术和条件下进行繁殖和生长.人们把那些尚未在实验室获得培养生长的微生物称之为未培养微生物(Uncultured microorganisms).本文概述了一些制约微生物培养生长的影响因素,重点介绍了近年来出现的一些新颖独特的环境微生物培养技术和方法,包括稀释培养法、高通量培养技术、模拟自然环境的扩散盒技术、土壤基质膜装置、细胞微囊包埋技术等.此外,本文还总结了通过改善微生物培养条件、设计开发新型的微生物培养基等方面取得的令人瞩目的进展.这些新颖培养技术和培养方法的出现,显著提高了微生物的可培养性,发现和鉴定了许多新的微生物物种,极大地丰富了可培养微生物的多样性和微生物资源,并为深入研究和开发微生物奠定了良好的资源研究基础.     

Changes in Sugar Content During Induction of Systemic Acquired Resistance to Late Blight Caused by Phytophthora infestans (Mont.) de Bary in Potato

Resistance of plants to their pathogens may be systemically enhanced by a localized induction treatment, a characteristic named systemic acquired resistance (SAR). Changes in amounts and proportions of sucrose, glucose and fructose were examined in induced and noninduced potato plants ( Solarium luberosum L. ev. Matilda) before, and 1–9 days after challenge inoculation. The potato plants were induced and challenged with Phytophthora infesians (Mont.) de Bary. Plants which were non-induced and non-challenged were also tested (referred to as non-treated). The sugars were analysed using high-performance anion exchange chromatography with pulsed electrochemical detection, HPAE-PED (Dionex system). The amounts as well as the proportions of sucrose, glucose and fructose were similar throughout the experimental period in the non-treated plants. In induced plants, before challenge inoculation, the amount of sucrose was 44% lower than in non-treated plants. One day after challenge inoculation, the amount of sucrose had decreased by 79% in non-induced plants compared with non-treated plants, while the induced plants were much less affected. The total amount of all sugars were approximately the same 1 day hefore and 9 days after the challenge inoculation in ail treatments. However, 1 day after challenge inoculation, a 65% decrease in total amount was observed in the non-induced plants compared with the smaller reduction of 37% in the induced plants. The large differences in sugar amounts and proportions between the different treatments are discussed.     

Root and shoot jasmonic acid induction differently affects the foraging behavior of <Emphasis Type="Italic">Cotesia glomerata</Emphasis> under semi-field conditions

Plants can accumulate and release defensive chemicals by activating various signaling pathways when they are damaged by herbivores or pathogens. The jasmonic acid pathway is activated after damage by chewing herbivores. Here we used jasmonic acid (JA) as an exogenous elicitor to induce feral cabbage plants. In this study, the effects of root JA (RJA) and shoot JA (SJA) induction on the foraging behavior of Cotesia glomerata, a parasitoid of the large cabbage white butterfly Pieris brassicae, was investigated under semi-field conditions. In all combinations of differently induced plants (RJA, SJA and control plants), the percentages of shoot induced plants that were visited by at least one wasp were significantly higher than those of controls or root induced plants during 3 h of foraging. Consequently, parasitism rates of P. brassicae on shoot-JA induced plants were significantly higher than on plants induced with JA to the roots or control plants in all tests. However, this behavioral preference was not reflected in the allocation of offspring. The clutch sizes of C. glomerata eggs on control, root induced and shoot induced plants were not significantly different from each other in two-choice or three-choice experiments, but did differ with clutch size in the two-choice experiment of uninduced control plants versus SJA. This semi-field study helps to further understand the choice behavior and preferences of parasitoids in natural multitrophic communities in which plants induced with root or shoot herbivores occur together.     

Changes in the Growth of Roots and Shoots when Perilla frutescens L. Britt. is Induced to Flower

The pattern of root and shoot growth of Perilla frutescens L.Britt. was studied in plants growing either in norally inductivephotoperiods or in non-inductive photoperiods. By the 20th dayof inductive treatment, that is at least 5 d before the firstflowers were pollinated, the rate of dry matter accumulationin the roots was slower in induced than in non-induced plants.The roots of induced plants had both a smaller fresh weightand dry weight per unit length. The rate of root elongationalso became slower in induced plants than in non-induced plants.The frequency of branching was greater in roots of induced plants.Plants exposed to inductive photoperiods showed precocious developmentof axillary buds on the shoot, and a reduction in the rate ofstem elongation. It is suggested that these changes in the shootreflect a decrease in the auxin status of the shoot, which mayin turn be responsible for the decreased rate of root growthin the induced plants.     

Characterization of induced resistance in tomato plants

We have characterized, using several types of bioassays, the resistance induced in young tomato plants by feeding of the corn earworm, Helicoverpa zea. Beet armyworm larvae, Spodoptera exigua, and leafminers, Liriomyza trifolii, were used to assay the induced resistance. In whole-plant experiments, damage localized to a single leaflet of fourleaf tomato plants induced a systemic increase in resistance such that beet armyworm larvae confined to previously damaged (induced) plants grew at a rate about half that of larvae raised on control plants and consumed less leaf tissue from induced plants than from control plants. In experiments using excised leaves, beet armyworm larvae suffered increased mortality when reared on leaves from induced plants. The strength of this induced resistance varied spatially relative to the damaged position; moreover, the spatial distribution of induced resistance changed over a three-week period following damage. Other experiments demonstrated that the mechanisms of induced resistance in tomato foliage involves both a decrease in larval preference for and a decrease in the nutritional value of induced foliage. Induction also retarded the oviposition and/or early development of leafminers. Thus, induced resistance has relatively severe effects on the biology of subsequent herbivores. These data should allow us to begin to elucidate cause-effect relationships between induced resistance and induced chemistry in tomato plants.     

Senescence of detached leaves in pigeon pea and chick pea: Regulation by developing pods

The senescence rate of the subtending leaves in deflowered and control plants of pigeon pea ICajanus cajan (L.) Millsp. cv., Prabhat] and chick pea ( Cicer arietinum L. cv. JG 62) were examined during the course of natural and induced senescence, at several stages of pod growth. The leaves from the top 5 nodes on the main axis in pigeon pea and the top 8 nodes on the main axis in chick pea were used throughout the experiments. The natural senescence was characterized in leaves taken directly from the field-growing plants. For the study of induced senescence, the leaves were excised from both control and deflowered plants at various stages of pod growth and placed in test tubes containing water under dark conditions. Senescence was assessed in terms of peroxidase activity and contents of tola] chlorophyll, soluble amino acids and total protein. During natural ageing in the field, the leaves from deflowered plants exhibited delayed senescence in both the species. In contrast, the rate of ageing during induced senescence was higher in the leaves of deflowered plants than in the controls. Although of the same chronological age when excised for induced senescence, the leaves of deflowered plants were evideatly metabolically different from the controls, due to the fact that deflowered plants did not support the development of pods. This difference probably determined the subsequent rate of induced senescence.     

Changes in the polypeptide profiles during photoinduction of Xanthium strumarium

The polypeptides in the leaf blades, petioles and apices from photoinduced and noninduced Xanthium strumarium L. were compared by two dimensional gel-electrophoresis. A 15 kDa and a 16 kDa polypeptide were detected in gels of the leaf blade from noninduced, but not from induced, plants. Similarly, an acidic 9 kDa polypeptide was detected in the apices from noninduced plants, but not in apices from induced plants. Both the apices and petioles from noninduced plants showed a 34 kDa polypeptide which was absent in tissues from induced plants. Thus, the disappearence of identifiable polypeptides from photoinduced tissues may be associated with the photoinductive short-day treatment that leads to flowering.     

甜叶菊同源四倍体离体诱导及鉴定

用不同浓度秋水仙素溶液处理甜叶菊不定芽,诱导同源四倍体,并进行解剖学、染色体鉴定和流式细胞仪鉴定倍性。结果表明:(1)用0.20%的秋水仙素溶液浸泡甜叶菊不定芽12h,同源四倍体诱导率最高,可达32.14%。(2)同源四倍体植株与二倍体(对照)相比,其气孔、叶片等均表现巨大性,且叶片变厚、叶色浓绿、叶片皱缩。(3)对照植株染色体2n=2x=22,四倍体植株染色体2n=4x=44;流式细胞仪倍性鉴定结果显示,对照DNA相对含量为100,四倍体DNA相对含量为200。(4)该研究共鉴定出48株甜叶菊同源四倍体植株,为进行倍性植株的诱导奠定了技术基础,为进一步开展甜叶菊同源四倍体新品种的选育提供了实验材料。     

Changes in the Protein Composition of the Shoot Apical Bud of Sinapis alba in Transition to Flowering

Vegetative plants of Sinapis alba L. grown in short days were induced to flower by expsoure to one or continuous long days. In both inductive conditions, the first flowers were initiated about 60 h after the start of the treatment. Soluble protein extracts were prepared from apical buds and just-expanded leaves of both vegetative and induced plants. Rabbit antisera were prepared using extracts from vegetative and reproductive buds. Immunodiffusion tests were performed. Analysis of the precipitin bands indicated that: (1) one antigenic protein was present in the vegetative buds and disappeared from the buds of induced plants between 96 and 240 h after the start of the inductive treatment; (2) the concentration of a another antigenic protein increased in buds of induced plants 30 h after the start of the inductive treatment; (3) the concentration of a third antigenic proteín increased in buds of induced plants at 96 h.     

Induced responses in Nicotiana attenuata affect behavior and growth of the specialist herbivore Manduca sexta

Many plants employ induced responses against generalist herbivores. Specialist herbivores, however, may employ several mechanisms to overcome the negative effects of induced plant defenses. Here we test how the behavior and development of specialist Manduca sexta larvae are affected by induced responses in their natural host plant Nicotiana attenuata. On a spatial scale relevant to both the plant and the herbivore, we first determined how methyl jasmonate (MeJA)-induced responses, such as increased nicotine production, affect the tendency of larvae to leave induced plants. When larvae were allowed to move between two plants planted in one pot, they left an MeJA-treated plant faster than a control plant. When both plants in the pot were MeJA-treated, the larvae developed more slowly than when both plants were uninduced, or when the larvae had the opportunity to move to an uninduced neighbor. The sooner larvae moved from an MeJA-treated plant to an untreated neighbor, the larger the body mass they attained. This demonstrates that M. sexta larvae can compensate behaviorally for the deleterious effects of induced plant responses. These effects were observed in plants grown under both low and high N supply rates, though the effects were more pronounced under high N. To examine the consequences of the timing and the direction of the host plant switching behavior for larval development, neonate larvae were fed leaves excised from induced and uninduced plants. Larvae confined to MeJA-treated leaves had higher mortality rates and grew slower than larvae fed only control leaves. This demonstrates that MeJA-induced responses decrease growth and development of specialist herbivores that do not have the behavioral option of moving to an uninduced plant. The sooner the larvae were switched to MeJA-treated leaves, the slower their development compared to larvae fed only uninduced leaves. In contrast, the sooner larvae fed MeJA-treated leaves were switched to control leaves, the faster they developed. Again the effects of MeJA treatment were stronger in plants grown under high N supply. We propose that induced plants growing in close competition with an uninduced conspecific may offset the fitness costs of these induced responses and perhaps obtain a fitness benefit by motivating herbivores to move to their neighboring competitors. Received: 25 March 1999 / Accepted: 8 October 1999     

Response of natural populations of predators and parasitoids to artificially induced volatile emissions in maize plants (Zea mays L.)

1 In response to herbivore attack, maize plants (Zea mays L.) emit a specific blend of induced volatiles. Artificial damage and subsequent treatment of the damaged site with caterpillar regurgitant induces the same response. The induced volatile chemicals are known to be highly attractive to several parasitoids of herbivores in laboratory bioassays, but very limited information is available on how the plant odours affect entomophagous insects in the field. 2 Experiments were conducted to determine if induced maize volatiles attract parasitic and predatory insects under field conditions and whether they affect their spatial distribution. 3 In a preliminary field experiment with blue sticky traps near treated (damaged and treated with caterpillar regurgitant) and healthy plants, more entomophagous insects (total number of parasitic Hymenoptera, Anthocoridae and Syrphidae) were trapped near treated plants than near healthy plants. 4 In a second experiment, attraction to the induced volatiles was monitored with sticky traps placed next to treated and healthy maize plants in a regular maize field. No significant differences between the two treatments were found, but significantly more insects (parasitic wasps, thrips and anthocorid bugs) were trapped near to the top of plants than on traps placed near the mid‐stem. Displacement of these insect groups within the field seemed to occur principally over the canopy, but under severe weather conditions they travelled lower in the canopy. 5 In a third experiment, the effect of induced maize odours on the spatial distribution of predators and parasitoids was investigated by placing sticky traps at different distances from healthy and treated plants. The higher catches of parasitoids near treated plants and the increased presence of these insects on the downwind side of treated plants support the notion that herbivore‐induced maize odours attract natural enemies of maize pests in the field.