Biosynthesis of a trypanocide by Chromobacterium violaceum

Radio-isotope studies indicated not only that l-tryptophan can serve as carbon source for synthesis of the trypanocide, violacein by Chromobacterium violaceum (BB-78 strain) but also that isatin and indole 3-acetic acid are both important metabolic intermediates. Using 3-indolyl [2-¹⁴C] and [1-¹⁴C] acetic acid, it was found that the carboxylic carbon was not eliminated and that indole-3-acetic acid was incorporated intact into the pigment structure. N-Ethyl(5-hydroxy-indol-3-yl)-2-indolylethylamide is also an important metabolic intermediate in the violacein biosynthesis. This is the first report of a metabolic scheme for violacein synthesis which includes an intermediate other than l-tryptophan.     

两种网柄细胞状黏菌挥发性成分

采用固相微萃取气相色谱-质谱联用技术,对紫轮柄菌Polysphondylium violaceum和簇生岐柄菌Cavenderia fasciculata子实体的挥发性成分进行分析,从这两种网柄细胞状黏菌中共鉴定出32种挥发性成分,包括烃、醛、吲哚、萜、酮、酯和酚类化合物。其中,紫轮柄菌P. violaceum的挥发性成分有15种化合物,簇生岐柄菌C. fasciculata的挥发性成分有27种化合物,二者共有化合物11种,部分化合物可用于制作香料等,研究结果为网柄细胞状黏菌的进一步应用提供了理论依据。     

川明参果实发育过程中解剖结构的变化

对伞形科(Apiaceae)中国特有单型属种类川明参（Chuanminshen violaceum Sheh et Shan）幼果发育阶段（包含幼果期Ⅰ、幼果期Ⅱ和幼果期Ⅲ）、中果发育阶段（包含中果期Ⅰ、中果期Ⅱ和中果期Ⅲ）和熟果发育阶段（包含熟果期Ⅰ、熟果期Ⅱ和熟果期Ⅲ）果实横切面的解剖结构进行了比较观察。观察结果表明,川明参果实在果壁细胞层数和形态、果棱和维管束、油管、胚乳以及分生果横切面大小和形状等特征均有明显的变化。川明参分生果果壁由厚变薄且外果壁、中果壁细胞形态发生变化,内果壁细胞消失;果实中油管分布在果实的背面、侧面和合生面,油管不断向外扩大,在成熟果实中油管往往皱缩。川明参果实中胚乳逐渐增大,从近球形变化为桃形、肾形直至月牙形,背部呈山丘状隆起;分生果横切面的形状由近五边状圆形变化至梭形,背腹极度压扁。通过对果实发育形态解剖观察发现,果实发育前期,果形的变化主要依靠维管束的发育,从而造成果棱的改变,来改变果实外部结构。到了熟果期,胚乳显现,形体变大,它的形状变化开始改变分生果的外部形态,并且影响较为显著。     

Production, extraction and purificationof violacein: an antibiotic pigment producedby Chromobacterium violaceum

A procedure for the production, extraction, and purification of violacein was developed using Chromobacterium violaceum (CCT 3496) cultivated on cotton, in modified 1 litre Roux bottles. A surface tray bioreactor was built to perform these experiments. Violacein was extracted with commercial ethanol, and purified by filtration, Soxhlet extraction, crystallization and high performance liquid chromatography. The violacein was analysed and identified by proton and carbon-13 NMR spectroscopies, thermogravimetric analysis, mass spectrometry, UV-VIS spectroscopy and infrared spectroscopy. It was concluded that the product was highly purified violacein.     

The Serratia-type hemolysin of Chromobacterium violaceum

Chromobacterium violaceum is a Gram-negative opportunistic human pathogen and an inhabitant of tropical soils and waterways. Although known primarily for the synthesis of the pigment violacein, and more recently as a reporter strain for quorum sensing, clinical reports of chromobacteriosis comprise the largest block of published literature on this organism. Genome sequencing has revealed many potential virulence factors in this microorganism, and this paper establishes the presence in C. violaceum of a Serratia type-hemolysin (ChlA) and transporter (ChlB). We also show that the hemolysin operon includes a third gene (chlC) that is predicted to encode a phosphorylation domain similar to the receiver domain of response regulators in bacterial signal transduction systems.     

Genotyping of Chromobacterium violaceum isolates by recA PCR-RFLP analysis

Intraspecies variation of Chromobacterium violaceum was examined by comparative sequence - and by restriction fragment length polymorphism analysis of the recombinase A gene (recA-PCR-RFLP). Primers deduced from the known recA gene sequence of the type strain C. violaceum ATCC 12472(T) allowed the specific amplification of a 1040bp recA fragment from each of the 13 C. violaceum strains investigated, whereas other closely related organisms tested negative. HindII-PstI-recA RFLP analysis generated from 13 representative C. violaceum strains enabled us to identify at least three different genospecies. In conclusion, analysis of the recA gene provides a rapid and robust nucleotide sequence-based approach to specifically identify and classify C. violaceum on genospecies level.     

A Stilbene Optical Brightener can Enhance Bacterial Pathogenicity to Gypsy Moth (Lepidoptera: Lymantriidae) and Colorado Potato Beetle (Coleoptera: Chrysomelidae)

Stilbene optical brighteners were first investigated to protect biological control agents such as viruses, fungi, and nematodes against ultraviolet light. Some are known to enhance the activity of insect viruses in Lepidoptera. In this work, one stilbene brightener, Tinopal LPW, also increased mortality of gypsy moth and Colorado potato beetle larvae when treated with bacteria/optical brightener combinations. This increase in mortality, however, did not occur for every bacteria/insect combination. In gypsy moth, a significant increase in larval mortality was observed only with Bacillus thuringiensis combined with Tinopal LPW. In Colorado potato beetle, however, the addition of Tinopal LPW increased larval mortality with all bacteria tested (B. thuringiensis, Serratia marcescens, Photorhabdus luminescens, and Chromobacterium sp.). The brightener also decreased the time to kill for these pathogens. This decrease in LT₅₀ was observed not only for bacteria+Tinopal LPW combinations, but also for combinations of Chromobacterium sp. toxin+Tinopal LPW. The mechanism for increase in bacterial toxicity by optical brighteners is compatible with mechanisms proposed for enhancement based on viral/lepidopteran/optical brightener systems that are not dependent on replication.     

Violacein transformation by peroxidases and oxidases: implications on its biological properties

1,3-Dihydro-2H-indol-2-one derivative (violacein) is extracted from Chromobacterium violaceum and presents several biological activities as antibiotic, antitumoral, antichagasic and antioxidant. In order to increase its biological activities and decrease its toxicity, one strategy is to slightly transform the molecules through a specific group transformation. Peroxidases, which are hemoproteins, are known as excellent oxidants producing hydroxylation and ring cleavage. Laccases are phenol oxidases produced by fungi as plants and belong to the oxidase group which complexes copper. This enzyme generates phenolates, quinones and also ring cleavage even in the presence of a mediator as 1-hydroxybenzotriazol (HBT). Lignin peroxidase and manganese peroxidase (LiP/MnP) pool from Phanerochaete chrysosporium, Horseradish peroxidase (HRP-VI) from horseradish, Lactoperoxidase (LPO) from bovine milk and Laccase (Lac) from Trametes versicolor acting on violacein were studied. Kinetics parameters and products distribution indicated a fast and efficient violacein transformation with all of them. HRP-VI acting on violacein was studied in details and spectral evidence indicated that Horseradish peroxidase compound II was formed during the oxidation reaction. Similar behavior with LiP/MnP pool was observed. Laccase, in the presence and absence of mediator (HBT), also showed a rapid violacein transformation. In a more detailed study with the HRP-VI reaction, a hydroxilation in the indol unit and a ring contraction of the pyrrol moiety of violacein molecule occurred.     

Biogenic production of cyanide and its application to gold recovery

Chromobacterium violaceum is a cyanogenic (cyanide-producing) microorganism. Cyanide is used on an industrial scale to complex and recover gold from ores or concentrates of ores bearing the precious metal. A potentially useful approach in gold mining operations could be to produce cyanide biologically in relatively small quantities at the ore surface. In this study, C. violaceum grown in nutrient broth formed a biofilm and could complex and solubilize 100% of the gold on glass test slides within 4–7 days. Approximately 50% of the cyanide-recoverable gold could be mobilized from a biooxidized sulfidic-ore concentrate. Complexation of cyanide in solution by gold appeared to have a beneficial effect on cell growth — viable cell counts were nearly two orders of magnitude greater in the presence of gold-coated slides or biooxidized ore substrates than in their absence. C. violaceum was cyanogenic when grown in alternative feedstocks. When grown in a mineral salt solution supplemented with 13.3% v/v swine fecal material (SFM), cells exhibited pigmentation and suspended cell concentrations comparable to cultures grown in nutrient broth. Glycine supplements stimulated production of cyanide in 13.3% v/v SFM. In contrast, glycine was inhibitory when added at the time of inoculation in the more concentrated SFM, decreasing cell numbers and reducing ultimate bulk-solution cyanide concentrations. However, aeration and addition of glycine to stationary phase cells grown on 13.3% v/v SFM anaerobically resulted in rapid production and high concentrations (up to 38 mg l⁻¹) of cyanide. This indicates that biogenesis of cyanide may be supported in remote areas using locally produced and inexpensive agricultural feedstocks in place of commercial media. Journal of Industrial Microbiology & Biotechnology (2001) 26, 134–139. Received 06 June 2000/ Accepted in revised form 30 September 2000     

Efficacy of biopesticides on spotted wing drosophila,Drosophila suzukii Matsumura in fall red raspberries

Drosophila suzukii Matsumura is a significant pest of soft‐skinned fruit. Larvae of D. suzukii develop within the fruit making it unmarketable as fresh berries and increasing the risk of rejection by processors. We evaluated selected biopesticides for control of D. suzukii in fall red raspberries, Rubus idaeus L. The trial results highlight a small number of biopesticides with the potential to reduce infestation of Drosophila larvae in raspberries. In addition to the standard biopesticide spinosad, we found that sabadilla alkaloids and Chromobacterium subtsugae both reduced the number of Drosophila larvae in raspberry fruit. Treatments that included corn syrup as a feeding stimulant showed no significant difference in their infestation levels compared to treatments without the syrup. In the final week of the 5‐week trial, treatments with rotations of either spinosad/C. subtsugae or spinosad/sabadilla alkaloids had a 67% and 57% reduction in infestation when compared to untreated raspberries. Treatments of spinosad alone on a 7 day rotation and C. subtsugae alone on a 3–5 day rotation both had a 62% and 61% reduction in larval infestation when compared to untreated raspberries. Third instar larvae, the largest and most damaging, were significantly reduced in plots treated with spinosad only, a rotation of spinosad/sabadilla alkaloids and the rotation of spinosad/C. subtsugae with corn syrup added when compared to untreated plots. This suggests that either of these biopesticides could be used as effective rotation partners along with spinosad for control of D. suzukii. Our results highlight that biopesticides can provide significant reduction in this devastating pest when used alone or in combination, providing options to support resistance management.