Biostimulants Derived from Moroccan Seaweeds: Seed Germination Metabolomics and Growth Promotion of Tomato Plant

Polysaccharides extracted from seaweeds can function as plant biostimulants. The aim of this study was to assess the effects of Polysaccharide Enriched Extracts (PEEs) obtained from 17 Moroccan seaweeds, on tomato seed germination and plant growth. Three concentrations (0.02, 0.05 and 0.1 mg mL⁻¹) of PEEs were applied to tomato seeds to evaluate their effect on 3 germination parameters: germination percentage (GP), germination speed (GS) and mean germination time (MGT). Metabolomic analysis by GC–MS was subsequently performed on seedlings. In the second experiment, four PEEs concentrations (0.02, 0.05, 0.1 and 0.2 mg mL⁻¹) were used as foliar spray or as soil application to tomato plants. Their growth parameters (number of leaves, shoot length, fresh and dry weight of stem and roots) and biochemical parameters (chlorophyll a and b) were measured. Results indicated a significant increase of GP and GS associated with a significant reduction of MGT of tomato seeds treated with 0.02 mg mL⁻¹ of PEEs obtained from Gigartina sp., Gigartina pistillata, Chondracanthus acicularis, Gelidium crinale, Schizymenia dubyi, Cystoseira. foeniculacea and Fucus spiralis. Similar results were also obtained by application of higher PEEs concentration (0.1 mg mL⁻¹) extracted from Ulva rigida, Codium tomentosum, Codium decorticatum and Bifurcaria bifurcata. Metabolomic analysis on seedlings detected the presence of some metabolites which could possibly be involved in seed germination enhancement or inhibition. The results of the second experiment showed that the same PEEs cited above at the same concentrations enhanced plant dry weight and chlorophyll a content except Gigartina sp., C. foeniculacea and C. decorticatum. Furthermore, soil application of PEEs was more effective in improving plant growth parameters than foliar application. The study shows the potential of PEEs from Moroccan seaweed to be used as biostimulants for a sustainable agriculture.

     

77种植物提取物对植物病原菌的生长抑制作用

以稻瘟病菌(Pyricularia grisea),水稻恶苗病菌(Fusarium moniliforme),玉米大斑病菌(Exserohilum turci-cum)等12种植物病原菌为供试菌种,采用生长速率法对77种植物的95%乙醇提取物在200μg/mL下进行室内抑菌试验。结果表明有15种植物提取物对植物病原菌有抑制作用,其中华山姜、硬骨藤、龙舌兰、红蒜、大花哥纳香、海南草珊瑚对至少一种菌的抑制率在50%以上,版纳青梅、大果巴戟、华山姜等8种植物提取物对至少三种病原菌均有不同程度的抑制作用。红蒜提取物对百合炭疽病菌、海南草珊瑚提取物对番茄灰霉病菌,以及龙舌兰提取物对玉米大斑病菌的抑制率分别为61.4%、70.7%、76.6%,与阳性对照抑制率相比效果明显。     

Growth Stimulants in Plant Extracts for Leuconostoc citrovorum

The growth of Leuconostoc citrovorum ML 34, an isolate associated with the malo-lactic fermentation of wine, was stimulated in part by grape, orange, cabbage, and tomato juices. The stimulatory activity of tomato serum was associated with the carbohydrate fraction. Further purification of the fraction showed that fructose was the factor responsible for initiating growth. In addition to fructose, the organism required CO(2) for establishing growth. Saturated CO(2) atmosphere and catalytic amounts of fructose served as substitutes for plant extracts in a complex glucose medium.     

三种植物提取物对菟丝子及大豆生长发育和宿主保护酶活性的影响

利用不同浓度的苦楝树皮和叶、隆缘桉叶和乌桕叶的乙醇提取物对菟丝子及其宿主大豆幼苗进行处理,15d后评价三种提取物对菟丝子和大豆幼苗的影响。结果表明:三种提取物在低浓度时对菟丝子及其宿主大豆幼苗生长发育均无显著影响,在高浓度(0.25g/mL)下,桉树叶提取物对大豆和菟丝子的损伤程度分别达到了64%和70%,苦楝树皮提取物对菟丝子损伤程度为78%,但对大豆幼苗仅为7%。桉树叶和苦楝树皮提取物处理均导致大豆叶片超氧化物歧化酶(SOD)活性升高,最高值分别为相应对照组的2.37倍和2.0倍;但对过氧化物酶(POD)和过氧化氢酶(CAT)活性的影响不同,桉树叶提取物使大豆幼苗POD活性最大值为对照组的2.28倍,而苦楝树皮提取物处理则是CAT活性升高,最大值为对照组的1.58倍,提示桉树叶提取物对大豆较强的伤害作用与其较低的CAT活性有关。     

Tropical Plant Extracts Modulating the Growth of Mycobacterium ulcerans

Mycobacterium ulcerans, the etiologic agent of Buruli ulcer, has been detected on aquatic plants in endemic tropical regions. Here, we tested the effect of several tropical plant extracts on the growth of M. ulcerans and the closely related Mycobacterium marinum. M. ulcerans and M. marinum were inoculated on Middlebrook 7H11 medium with and without extracts from tropical aquatic plants, including Ammannia gracilis, Crinum calamistratum, Echinodorus africanus, Vallisneria nana and Vallisneria torta. Delay of detection of the first colony and the number of colonies at day 7 (M. marinum) or day 16 (M. ulcerans) were used as endpoints. The first M. ulcerans colonies were detected at 8 ± 0 days on control Middlebrook 7H11 medium, 6.34 ± 0.75 days on A. gracilis-enriched medium (p<0.01), 6 ± 1 days on E. africanus- and V. torta-enriched media (p<0.01), 6 ± 0 days on V. nana-enriched medium (p<0.01) and 5.67 ± 0.47 days on C. calamistratum-enriched medium (p<0.01). Furthermore, the number of detected colonies was significantly increased in C. calamistratum- and E. africanus-enriched media at each time point compared to Middlebrook 7H11 (p<0.05). V. nana- and V. torta-enriched media significantly increased the number of detected colonies starting from day 6 and day 10, respectively (p<0.001). At the opposite, A. gracilis-enriched medium significantly decreased the number of detected colonies starting from day 8 PI (p<0.05). In conclusion, some aquatic plant extracts, could be added as adjuvants to the Middlebrook 7H11 medium for the culturing of M. marinum and M. ulcerans.     

The Growth Substances separated from Plant Extracts by Chromatography. I

For 0·per cent. sodium nitrite read 0·5 per cent. potassium ferricyanide     

The Growth Substances separated from Plant Extracts by Chromatography. I

Methods for the chromatographic separation on paper of indolecompounds and for the direct biological assay of the chrornatograinsusing the Avena coleoptile straight-growth method are described.Reagents for the detection of the indole-3-carboxylic acids,indole-3-acetonitrile, and gramirte as coloured spots on chromatogramsare compared and the areas of such spots are shown to be proportionalto the logarithms of the quantities of substance present. The procedure of chromatography described is shown not to involvea loss of indole-3-acetic acid activity if chromatography isdone in darkness and chrornatograms are not stored in lightand air. Methods are described for the extraction of growth aubstancesfrom plant materials, the purification and chromatography, onpaper, of the extracts and the bioassay of the chromatogramsusing Avena coleoptile sections. The ether extracts, containing acidic substances, of etiolatedbroad bean and pea shoots and roots, etiolated sunflower shoots,maize roots, and potato etiolated shoots and tuber have beenchromatographed and the chromatograms bioassayed. On all chromatogramsthree areas active in Avena coleoptile section growth are found.One area of growth promotion is shown due to indole-3-aceticacid [IAA]. Another area of growth promotion and, one of growthinhibition are due to unknown substances, which are named accelerator () and inhibitor ß (ß) respectively. On chromatograms of potato tuber a fourth growth-promoting area,in addition to those described above, is detected and is shownto be probably due to indole-3-acetonitrile [IAN]. IAN or indole-3-pyruvicacid may occpr together with IAA on chrormatograms of extractsof immature maize kernels and cauliflower head respectively. On cabbage extract chromatograms the growth-promoting activitycorresponding in position with IAA is shown to be due to IAAand to IAA alone. In etiolated broad bean shoots IAA is the predominating growthsubstance in the stem and ß predominates in the firstlateral bud. The latter is suggested as an explanation of apicaldominance, and the predominance of ß in potato tuberskin is suggested as an explanation of dormancy in tubers. In the broad bean root the acidic growth-substance patterns,for the whole root and for the sections 0–2 cm. and 2–4cm. from the tip, are the same. The acidic growth substances extractable from broad bean shootsare the same whether the plant material is boiled or frozenbefore extraction.     

Phospholipids as Plant Growth Regulators

In this paper the potential to use phospholipids and lysophospholipids as plant growth regulators is discussed. Recent evidence shows that phospholipids and phospholipases play an important signalling role in the normal course of plant development and in the response of plants to abiotic and biotic stress. It is apparent that phospholipase A (PLA), C (PLC) and D (PLD), lysophospholipids, and phosphatidic acid (PA) are key components of plant lipid signalling pathways. By comparison, there is very little information available on the effect of exogenously applied phospholipids on plant growth and development. This paper serves to introduce phospholipids as a novel class of plant growth regulator for use in commercial plant production. The biochemistry and physiology of phospholipids is discussed in relation to studies in which phospholipids and lysophospholipids have been applied to plants and plant parts. Implicit in the observations is that phospholipids impact the hypersensitive response and systemic acquired resistance in plants to improve crop performance and product quality. Based on published data, a scheme outlining a possible mode of action of exogenously applied phospholipids is proposed.     

DNA甲基化与植物的生长发育

文章就DNA甲基化与植物生长发育的关系、催化甲基化的酶、5－甲基胞嘧啶在植物基因组中的分布、甲基化的发生和遗传的研究进展作了介绍。     

The Influence of Plant Extracts on Phytotoxin Production and Growth Rate of Alternaria helianthi

When liquid cultures of Alternaria helianthi were supplemented with aqueous extracts of leaf tissue of its host plant (sunflower), pronounced effects on both growth and production of the toxin deoxyradicinin were apparent. Very low levels of leaf extract stimulated toxin production but did not significantly affect growth, while higher levels markedly stimulated mycelial growth and at the same time toxin production was greatly suppressed. Leaf extracts of non-host plant species were also stimulatory to phytotoxin biosynthesis.     

Seaweed Oligosaccharides Stimulate Plant Growth by Enhancing Carbon and Nitrogen Assimilation, Basal Metabolism, and Cell Division

It is now well established that plant cell wall oligosaccharides can stimulate or inhibit growth and development in plants. In addition, it has been determined that seaweed (marine algae) cell wall polysaccharides and derived oligosaccharides can enhance growth in plants. In particular, oligo-alginates obtained by depolymerization of alginates from brown seaweeds increase growth of different plants by enhancing nitrogen assimilation and basal metabolism. Interestingly, oligo-alginates also stimulate growth of marine and fresh water green microalgae, increasing the content of fatty acids. On the other hand, oligo-carrageenans obtained by depolymerization of carrageenans from red seaweeds increase growth of tobacco plants by enhancing photosynthesis, nitrogen assimilation, basal metabolism, and cell division. In addition, oligo-carrageenans increase protection against viral, fungal, and bacterial infections in tobacco plants, which is determined, at least in part, by the accumulation of several phenylpropanoid compounds (PPCs) with antimicrobial activity. Moreover, oligo-carrageenans stimulate growth of 3-year-old Eucalyptus globulus trees by increasing photosynthesis, nitrogen assimilation, and basal metabolism. Furthermore, oligo-carrageenans induce an increase in cellulose content and in the level of essential oil and some PPCs with antimicrobial activities, suggesting that defense against pathogens may be also enhanced. Thus, seaweed oligosaccharides induce a dual beneficial effect in plants and trees, enhancing growth, which is determined by the increase in carbon and nitrogen assimilation, basal metabolism, and cell division, and defense against pathogens, which is determined by the accumulation of compounds with antimicrobial activities. In this sense, molecular mechanisms that potentially interconnect activation of plant growth and defense responses are discussed.     

天然植物提取物对肉鸭生长性能和屠宰性能的影响

采用单因子试验设计,研究了天然植物提取物对生长后期肉鸭生长性能和屠宰性能的影响.选择健康、体重相近(659.05±8.04 g)的14日龄天府肉鸭120只(公母各半),随机分为5个处理(4个试验组和1个对照组),每个处理4个重复,每个重复6只鸭(公母各半).基础日粮中分别添加37.5、75、150和225 mg/kg植物提取物即为相应的试验日粮,对照组饲喂基础日粮.试验期28 d.结果表明:①除225 mg/kg组降低采食量外,其余各组对采食量的影响不显著;②日粮中添加不同剂量植物提取物均提高了肉鸭试验各期的生长速度和饲料转化效率,与对照组相比,37.5,75,150和225 mg/kg植物提取物分别提高全期ADG 6.30%(P<0.05),7.07%(P<0.05),9.62%(P<0.01)和5.28%(P<0.05),分别降低全期F/G 4.60%(P<0.05),10.73%(P<0.01),8.81%(P<0.01)和14.56%(P<0.01).回归分析表明,全期ADG随植物提取物添加剂量呈显著二次曲线(P<0.05)上升,当添加剂量为132.75 mg/kg时,试验全期增重速度最大,达86.8 g/d;全期F/G随添加剂量增加呈极显著二次曲线下降(P<0.01);③植物提取物显著改善肉鸭的屠宰性能,显著提高瘦肉率(P<0.05),极显著降低腹脂沉积(P<0.01),且随添加剂量增加呈极显著二次曲线关系变化(P<0.001);④植物提取物在生长后期肉鸭日粮中的适宜添加剂量为150 mg/ks.结果提示,植物提取物可通过提高饲料利用效率显著改善生长后期肉鸭的生长性能和屠宰性能,且存在剂量效应.     

自体吞噬在植物生长发育中的功能

自体吞噬是一种细胞内自我降解系统,它能将植物细胞内溶物运输至液泡并降解.自体吞噬可划分为内溶物的包裹、运输至液泡、内溶物的降解和降解产物的重新利用几个连续步骤.关于细胞自体吞噬的认识主要来源于酵母、人类、小鼠、果蝇和线虫等生物,以拟南芥等为代表的植物细胞自体吞噬的研究虽然刚刚开始,但也取得了一些标志性的成果,且近十几年来已迅速成为植物研究领域的热点之一.自体吞噬在植物体内具有多种生理和病理作用,如对饥饿的适应、细胞内蛋白质和细胞器的清除、种子中贮藏蛋白的积累、抵制微生物、细胞死亡和胁迫响应等.本文在介绍自体吞噬形成过程的基础上,着重探讨了自体吞噬在植物生长发育中的功能,并对植物中自体吞噬的研究方向进行了展望.     

膨胀素在植物生长发育中的作用

膨胀素是一类具有非水解活性的细胞壁松弛蛋白,参与植物生长发育过程中细胞壁的修饰。大多数植物中都发现有膨胀素基因家族成员存在,其功能涉及植物生长发育的各个方面,包括营养生长、形态发生、受精授粉、果实成熟等,并表现出高度的组织、器官和细胞特异性。本文综述膨胀素在种子萌发、叶的发育、根茎生长、花的发育等生长发育过程中的作用。     

PPR蛋白在植物生长发育中的作用

PPR蛋白在陆生植物中属于最大的蛋白家族之一,其成员种类和数量均十分庞大。PPR蛋白主要的功能是通过在多种细胞器中进行定位从而参与细胞核和细胞器中特异单链RNA的转录后修饰和编辑,在植物生长发育的多个阶段均发挥着重要的作用。多数PPR蛋白编码基因的突变体呈现异常的发育表型,如胚胎致死、发育迟缓及绿化延迟等。对近年来植物PPR蛋白的分类、定位、RNA修饰的机制及其对植物生长发育影响进行了综述,并展望了植物PPR发挥功能区域和参与的调控网络研究。     

类脂对植物生长和发育的作用

简述了类脂在植物生长和发育中的作用,特别是类脂中脂肪酸的饱和度对植物生长发育的影响,植物固醇对植物的表型和在低温下的生长、胚胎的发育以及可育性中的作用.     

多胺在植物生长发育过程中的生理作用

多胺在植物生长发育过程中具有广泛的生理作用,如参与植物衰老进程的调控、体细胞胚发生、花芽分化、花和果 实的发育及参与各种生理胁迫反应等。本文重点综述了多胺在植物生长发育过程中生理学功能方面的研究进展,并对有关 问题进行了讨论和展望。