Subcellular localization of enzymes of anthocyanin biosynthesis in protoplasts

Flavanone synthase, chalcone-flavanone isomerase and UDP-glucose; anthocyanidin-3-O-glucosyltransferase activities of protoplasts and subcellular fractions of protoplasts of Hippeastrum and Tulipa were investigated. Subcellular fractions studied were intact vacuoles, cytosol and particulate components of protoplasts less the vacuole. The cytosol fraction had the highest activity of the three enzymes studied. Results similar to those found for Hippeastrum were obtained with fractions from leaves and petals of Tulipa. The increase in flavanone synthase activity in the cytosol fraction from petals of Hippeastrum during development paralleled the increase in anthocyanin content of the petals.     

Subcellular localization of glucosyltransferases involved in cardiac glycoside glucosylation in leaves of Convallaria majalis

The glucosylation of convallatoxin and convallatoxol was investigated using homogenates and various subcellular fractions from leaves of Convallaria majalis. The enzyme activity reached a maximum about 5 weeks after the onset of flowering and was found distributed among the soluble and the light membrane fraction. Upon separation of the light membranes by sucrose density gradient centrifugation, glucosyltransferase activity was found solely in a fraction banding at a density of 1.07 g/cm³, which is thought to represent vacuole membranes.     

Studies on ethylene binding by cell-free preparations from cotyledons of Phaseolus vulgaris L.: subcellular localization

Abstract. Studies on the subcellular location of ethylene binding activity from developing cotyledons of Phaseolus vulgaris L. are described. Binding activity has been shown to be predominantly membrane bound. When separated by rate-zonal centrifugation more than 70% of this activity was of low sedimentation rate. The slowly sedimenting band of activity was further fractionated into three bands by isopycnic density gradient centrifugation. The three bands occur at sucrose densities of 1.125 g cm⁻³, 1.155 g cm⁻³ and 1.175 g cm⁻³, corresponding to the distribution of putative marker enzymes for the cell endomembrane system and to protein body membranes. Further circumstantial evidence was obtained by electron microscopy and sucrose step gradient centrifugation.     

Chloroplast cysteine synthases of Trifolium repens and Pisum sativum

About 68–86% of the cysteine synthase activity in leaf tissue of white clover (Trifolium repens) and peas (Pisum sativum cultivar Massey Gem) was associated with chloroplasts. The enzymes from white clover and peas were purified ca 66 and 12-fold respectively. For clover, the K_m values determined by calorimetric and S^2? ion electrode methods were: S^2? 0.51 and 0.13 mM; O-acetylserine (OAS), 3.5 and 2.O mM respectively. The analogous values for the pea enzyme were: S^2?, 0.24 and 0.06 mM; OAS, 3.1 and 0.24 mM. Both enzymes were inhibited by cystathionine and cysteine. Pretreatment with cysteine inactivated the enzyme, but addition of pyridoxal phosphate caused partial reactivation. Isolated pea chloroplasts (70–75 % intact) catalysed OAS-dependent assimilation of sulphide at a mean rate of 88 μmol/mg Chl/hr. About 85 % of the OAS-dependent sulphide assimilated was recovered as cysteine. The rates were unaffected by light and 2 μM DCMU. Sonicating the chloroplasts enhanced the rate by 1.3–2 fold. Cysteine synthase activity was associated with the chloroplast stroma. Similar results were obtained for clover chloroplasts except that both the intactness and the rates were lower.     

Subcellular localization of aphidicolin biosynthetic enzymes heterologously expressed in Aspergillus oryzae

The secondary metabolite aphidicolin has previously been produced by Aspergillus oryzae after the heterologous expression of four biosynthetic enzymes isolated from Phoma betae. In this study, we examined the subcellular localization of aphidicolin biosynthetic enzymes in A. oryzae. Fusion of green fluorescent protein to each enzyme showed that geranylgeranyl diphosphate synthase and terpene cyclase are localized to the cytoplasm and the two monooxygenases (PbP450-1 and PbP450-2) are localized to the endoplasmic reticulum (ER). Protease protection assays revealed that the catalytic domain of both PbP450s was cytoplasmic. Deletion of transmembrane domains from both PbP450s resulted in the loss of ER localization. Particularly, a PbP450-1 mutant lacking the transmembrane domain was localized to dot-like structures, but did not colocalize with any known organelle markers. Aphidicolin biosynthesis was nearly abrogated by deletion of the transmembrane domain from PbP450-1. These results suggest that ER localization of PbP450-1 is important for aphidicolin biosynthesis.     

Light induced changes in anthocyanin concentration,activity of phenylalanine ammonia-lyase and flavanone synthase and some of their properties in Brassica oleracea

Seedlings of red cabbage, Brassica oleracea cv Red Danish, germinated in the dark, rapidly produced anthocyanins upon illumination. The anthocyanin production increased up to six days of illumination time. The activity of phenylalanine ammonia-lyase increased rapidly in illuminated seedlings to a maximum at 8 hr and declined thereafter to dark levels. During this period the activity of flavanone synthase, the first enzyme responsible for the establishment of C₁₅ flavonoid skeleton, paralleled that of the anthocyanin concentration. The crude flavanone synthase has a pH optimum at around 8, a molecular weight of ca 120 000, and is able to utilize only p-coumaryl-CoA as co-substrate for the production of flavonoids.     

Subcellular localization of lipoxygenase and lipolytic acyl hydrolase enzymes in plants

The subeellular localization of two lipid-degrading enzymes, lipolytic acyl hydrolase (LAH) and lipoxygenase (LOX) was studied. In potato tubers the ac     

Subcellular localization of steroidal glycoalkaloids in vegetative organs of Lycopersicon esculentum and Solanum tuberosum

Cell fractions from the major vegetative organs of tomato and potato plants were obtained by homogenization and differential centrifugation. In both species, steroidal glycoalkaloids were found to accumulate mainly in the soluble fraction, with smaller amounts in the microsomal fraction. Alkaloids appeared sporadically in the mitochondrial fractions but were only detected in lower fractions as an artefact.     

Subcellular localization of luteolin glucuronides and related enzymes in rye mesophyll

Vacuoles were isolated by osmotic rupture of mesophyll protoplasts from the primary leaves of 4-d- and 7-d-old plants of rye (Secale cereale L.). Their content of two flavones, luteolin 7-O-[-d-glucuronosyl-(12)-d-glucuronide] (R₂) and luteolin 7-O-[-d-glucuronosy 1 (12) -d-glucuronide]-4-O--d-glucuronide (R₁), as well as that of three specific flavone-glucuronosyltransferases involved in their biosynthesis and of a specific -glucuronidase was determined in comparison to the parent protoplasts. The two flavonoids were found to be entirely located in the vacuolar fraction, together with 70% of the activity of UDP-glucuronate: luteolin 7-O-diglucuronide-4-O-glucuronosyl-transferase (LDT; EC 2.4.1.), the third enzyme of the sequence of three transferases in the anabolic pathway. The activities of the first and second anabolic enzymes, UDP-glucuronate: luteolin 7-O-glucuronosyltransferase (LGT; EC 2.4.1.) and UDP-glucuronate: luteolin 7-O-glucuronide-glucuronosyltransferase (LMT; EC 2.4.1.) could not be found in the vacuolar fraction in appreciable amounts. The specific -glucuronidase (EC 3.2.1.), catalyzing the deglucuronidation of luteolin triglucuronide to luteolin diglucuronide, was present with 90% of its activity in the digestion medium after isolation of mesophyll protoplasts, indicating an apoplastic localization of this enzyme. The data presented indicate a directed anabolic and subsequent catabolic pathway for the luteolin glucuronides in the mesophyll cells of rye primary leaves. This includes two cytosolic and a last vacuolar step of glucuronidation of luteolin, and the vacuolar storage of the luteolin triglucuronide. We propose the transport of the latter into the cell wall, after which the triglucuronide is deglucuronidated, this being the first step for further turnover.Dedicated to Professor Ludwig Bergmann, Botanisches Institut der Universität zu Köln, on the occasion of his 65th birthday     

Storage glucan biosynthesis in Cyanidium, Chlorella and Prototheca: evidence for endosymbiosis?

The storage glucans of Chlorella pyrenoidosa and Prototheca zopfii are identical and consist of a linear polyglucan akin to amylose and a branched amylopectin component. The branched glucans of these algae differ markedly from that formed by the hot-springs alga, Cyanidium caldarium. The more highly branched Cyanidium glucan appears to be formed by branching glucosyltransferases which are different from those of the other two algae. The relevance of the data to the possibility of Cyanidium being a Prototheca-like Chlorella that has acquired symbiotic Cyanobacteria as chloroplasts is discussed.     

Water stress, carbon dioxide, and light effects on sucrosephosphate synthase activity in Phaseolus vulgaris

The characteristics of sucrose-phosphate synthase (SPS; EC 2.4.1.14) activity in leaves of Phaseolus vulgaris L. cv. Linden was studied in plants subjected to water stress and various CO₂ and light treatments. When water was withheld for 3 days causing mild water stress (–0.9 MPa), the activity of SPS measured in crude extracts was reduced ca 50%. The effect of water stress was most evident when the enzyme was assayed with saturating amounts of its substrates fructose 6-phosphate and UDP glucose. Placing a water-stressed plant in an atmosphere containing 1% CO₂ reversed the effect of water stress on SPS activity over 5 h even though the water stress was not relieved. Holding unstressed leaves in low CO₂ partial pressure reduced the extractable activity of SPS. After 1 h of low CO₂ treatment the effect of low CO₂ could be reversed by 20 min of 5% CO₂. However, after 24 h of low CO₂ treatment, less SPS activity was recovered by the 20 min treatment. The cytosolic protein synthesis inhibitor cycloheximide prevented the slow recovery of SPS activity, but did not affect the rapid recovery of SPS. We conclude that the effect of water stress on SPS activity was a consequence of the inhibition of photosynthesis caused by stomatal closure. Responses of Phaseolus vulgaris SPS to light were similar to the response to low CO₂ in that the effects were most pronounced under V_max assay conditions. This is the first report of this type of light response of SPS in a dicotyledonous species.     

Expression of EGFP/SDCT1 fusion protein, subcellular localization signal analysis, tissue distribution and electrophysiological function study

A main pathway for energy ATP production inhuman body is by tricarboxylic acid cycle (Krebs cy-cle). Sodium-dependent dicarboxylate co-transporterprotein (SDCT, NaDC, NaC) is an organic aniontransporter protein family responsible for trans-mem- for 30 s, and extension 72℃ for 2 min; followed bybrane transport of Krebs cycle intermediate metabolite final extension 72℃ for 7 min. PCR products weresuch as succinate and citrate. They predominantly lo- …     

Subcellular site of carotenoid biosynthesis in Neurospora crassa

A cell-free system prepared from Neurospora crassa mycelia was capable of incorporating radioactivity from [¹⁴C]-mevalonic acid into phytoene and to a much lesser extent into more unsaturated carotenoids. Whereas carotenogenic activities were only minimal in extracts from dark-grown cultures, they were several-fold increased following a short in vivo illumination; this photo-induced increase was inhibited by cycloheximide. Subcellular localization of carotenogenic enzyme activities was investigated using incubations of particular isolated fractions, together with [¹⁴C]-mevalonic acid and a geranylgeranyl-pyrophosphate-synthesizing system provided by the endosperm of maturing pumpkin seeds. Maximum carotenogenic activity (ca 80%) was localized in two membrane fractions previously shown to contain plasma membranes and, in particular, membranes of the endoplasmic reticulum. The lipid layer, containing the bulk of carotenoid pigments, possesses only trace amounts of enzyme activities.     

Effect of ageing on enzymes of phenylpropanoid metabolism in Solanum tuberosum discs

-Separation of cell fractions or cell organelles of potato tuber by differential centrifugation and by sucrose density gradient centrifugation showed that, in dormant tissue, nearly all the activity of shikimate and prephenate dehydrogenases, phenylalanine ammonia lyase, cinnamate-4-hydroxylase and an O-methyltransferase for caffeate was in the soluble fraction. All these enzymes increased in activity in slices aged in light for 18 hr. In contrast to the other enzymes, cinnamate hydroxylase becomes associated with the microsomal fraction in aged discs.     

Glucosyltransferase isozymes forming storage glucan in prochloron, a prokaryotic green alga

Since the prokaryotic, green marine alga Prochloron has not, as yet, been cultured, lyophilized cells were used in a microadaptation of polyacrylamide gel electrophoresis (PAGE) in order to isolate the glucosyltransferase isozymes. The pattern obtained with these capillary gels was identical with those of cyanophytes. Besides two phosphorylase and synthase isozymes, three branching isozymes of the b.e. type were found to be present.     

铯对印度芥菜幼苗生长的影响及其亚细胞分布和化学形态

以印度芥菜为材料,用含铯(Cs+)[8.24(CK),25,50,100,200mg·L~(-1)]的Hoagland营养液培养印度芥菜种子和幼苗,采用IMAGE-J软件测定根、茎长度,通过差速离心法、化学试剂提取法分别提取幼苗根、茎、叶各亚细胞组分及不同化学形态的Cs+,并用火焰原子分光光度计测定Cs+含量,分析Cs+对幼苗生长的影响及其亚细胞分布和化学形态,进而探讨Cs+对植物的伤害机理。结果显示:(1)Cs+对印度芥菜幼苗生长具有明显的抑制作用,根、茎的EC50(相对抑制率达到50%的Cs+浓度)分别为112.09和118.42mg·L~(-1);(2)各器官中Cs+的积累量总体表现为叶根茎;Cs+在印度芥菜中的亚细胞分布呈现为可溶性组分细胞壁组分细胞器组分,三者所占比例分别为52.86%~79.19%、20.81%~45.05%和1.43%~9.00%;(3)Cs+在印度芥菜各器官中主要以无机盐和水溶态赋存,两种形态根、茎、叶占比分别达到88.02%~92.20%、97.33%~100%和95.06%~100%。研究表明:印度芥菜积累过量的Cs+可抑制其根、茎生长,导致叶片枯萎,主要是因为Cs+在印度芥菜体内大部分以无机盐态和水溶态形式存在,使Cs+在植物体内具有较强迁移能力和毒理生物有效性,更易分布到重金属的毒性敏感区(如细胞器),导致细胞器受到功能性损伤,从而使植物表现出明显中毒症状。     

十字花科黑腐病菌III型效应物XopXccR1植物亚细胞定位

[目的] 植物病原细菌通过III型分泌系统（type III secretion system,T3SS）将III型效应物（type III secreted effectors,T3SEs）分泌转运到宿主细胞的不同位点上,进而行使不同的致病功能。本研究旨在确定Xcc 8004 III型效应物中分子量最大的蛋白XopXccR1在植物中的亚细胞定位。[方法] 利用生物信息学方法分析XopXccR1的跨膜信息。通过同源重组方法将XopXccR1全长、N端（1–1220 aa）和C端（1221–2030 aa）分别克隆到植物表达载体pCAMBIA-2300-35S：：EGFP上,利用根癌农杆菌介导的瞬时表达浸染本生烟,通过激光共聚焦显微镜观察亚细胞定位结果。[结果] XopXccR1全长和N端定位在本生烟细胞膜上,而C端定位在细胞质中。[结论] XopXccR1的N端与C端可能分别存在定位信号,N端信号主导全长蛋白的最终定位。     

Flavanone synthase from cell suspension cultures of Haplopappus gracilis and comparison with the synthase from parsley

Flavanone synthase was isolated and purified ca 62-fold from cell suspension cultures of Haplopappus gracilis. The enzyme preparation catalysed the formation of naringenin from 4-coumaryl-CoA and malonyl-CoA with a pH optimum of ca 8. The same enzyme was also capable of synthesizing eriodictyol from caffeyl-CoA and malonyl-CoA; in this case the pH optimum lay between 6.5 and 7. The homogeneous flavanone synthase from cell suspension cultures of parsley showed the same dependence of the pH optimum on the nature of the cinnamyl-CoA. It can be concluded that both naringenin and eriodictyol are natural products of the synthase reaction.