Precursor-feeding and altered-growth conditions reveal novel blue pigment production by Rubrivivax benzoatilyticus JA2

2019 ◽  
Vol 41 (6-7) ◽  
pp. 813-822
Author(s):  
Lakshmi Prasuna Mekala ◽  
Mujahid Mohammed ◽  
Sasikala Chintalapati ◽  
Venkata Ramana Chintalapati
2019 ◽  
Vol 5 (2) ◽  
pp. 46 ◽  
Author(s):  
Stephanie Stange ◽  
Susanne Steudler ◽  
Hubertus Delenk ◽  
Anett Werner ◽  
Thomas Walther ◽  
...  

The soft rot fungus Chlorociboria aeruginascens produces a blue–green pigment xylindein, which is of considerable interest for various applications such as in the veneer industry or in organic semiconductors. To understand the fungal growth as well as pigment production of C. aeruginascens, several studies were performed, the results of which are presented here. These studies investigated various growth conditions such as temperature, pH value, oxygen level and light intensity. It was observed that the formation of xylindein by C. aeruginascens decoupled from growth. In the primary metabolismus, the uncolored biomass is formed. Pigment production took place within the secondary metabolism, while biomass growth as well as pigment production depended on various growth conditions. It was also found that certain conditions encourage the switch in metabolism, leading to pigment production.


1994 ◽  
Vol 11 (6) ◽  
pp. 1127-1139 ◽  
Author(s):  
Sylvie Reverchon ◽  
William Nasser ◽  
Janine Robert-Baudouy

2016 ◽  
Vol 79 (8) ◽  
pp. 1430-1435 ◽  
Author(s):  
MARGHERITA CHIERICI ◽  
CLAUDIA PICOZZI ◽  
MARISA GRAZIA LA SPINA ◽  
CARLA ORSI ◽  
ILEANA VIGENTINI ◽  
...  

ABSTRACT The blue discoloration in Mozzarella cheese comes from bacterial spoilage due to contamination with Pseudomonas. Fourteen Pseudomonas fluorescens strains from international collections and 55 new isolates of dominant bacterial populations from spoiled fresh cheese samples were examined to assess genotypic and phenotypic strain diversity. Isolates were identified by 16S rRNA gene sequencing and tested for the production of the blue pigment at various temperatures on Mascarpone agar and in Mozzarella preserving fluid (the salty water in which the cheese is conserved, which becomes enriched by cheese minerals and peptides during storage). Pulsed-field gel electrophoresis analysis after treatment with the endonuclease SpeI separated the isolates into 42 genotypes at a similarity level of 80%. Based on the pulsotype clustering, 12 representative strains producing the blue discoloration were chosen for the multilocus sequence typing targeting the gyrB, glnS, ileS, nuoD, recA, rpoB, and rpoD genes. Four new sequence typing profiles were discovered, and the concatenated sequences of the investigated loci grouped the tested strains into the so-called “blue branch” of the P. fluorescens phylogenetic tree, confirming the linkage between pigment production and a specific genomic cluster. Growth temperature affected pigment production; the blue discoloration appeared at 4 and 14°C but not at 30°C. Similarly, the carbon source influenced the phenomenon; the blue phenotype was generated in the presence of glucose but not in the presence of galactose, sodium succinate, sodium citrate, or sodium lactate.


1988 ◽  
Vol 66 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Masakatsu Yanagimoto ◽  
Kunisuke Matsumoto ◽  
Katsumi Mori

2009 ◽  
Vol 2009 ◽  
pp. 1-7 ◽  
Author(s):  
Hans-Peter Grossart ◽  
Marc Thorwest ◽  
Inken Plitzko ◽  
Thorsten Brinkhoff ◽  
Meinhard Simon ◽  
...  

Twoγ-Proteobacteriastrains, that is, HP1 and HP9, which both produce a diffusible deep blue pigment, were isolated from the German Wadden Sea and from the Øresund, Denmark, respectively. Both strains affiliate with the genusRheinheimera. Small amounts of the pigment could be extracted from HP1 grown in a 50 L fermenter and were purified chromatographically. Chemical analysis of the pigment including NMR and mass spectrometry led to a molecular formula ofC34H56N4O4(m.w. 584.85) which has not yet been reported in literature. The molecule is highly symmetrically and consists of two heterocyclic halves to which aliphatic side chains are attached. The pigment has been named glaukothalin due to its blue color and its marine origin (glaukos,gr.=blue,thalatta,gr.=sea). Production of glaukothalin on MB2216 agar plates by ourRheinheimerastrains is affected in the presence of other bacterial strains either increasing or decreasing pigment production. The addition of a single amino acid, arginine (5 gl−1), greatly increases pigment production by ourRheinheimerastrains. Even though the production of glaukothalin leads to inhibitory activity against three bacterial strains from marine particles, ourRheinheimeraisolates are inhibited by various bacteria of different phylogenetic groups. The ecological role of glaukothalin production byRheinheimerastrains, however, remains largely unknown.


2010 ◽  
Vol 77 (1) ◽  
pp. 172-178 ◽  
Author(s):  
Hiroshi Fujikawa ◽  
Ryo Akimoto

ABSTRACTA bacterium capable of producing a deep blue pigment was isolated from the environment and identified asPantoea agglomerans. The pigment production characteristics of the bacterium under various conditions were studied. The optimal agar plate ingredients for pigment production by the bacterium were first studied: the optimal ingredients were 5 g/liter glucose, 10 g/liter tryptic soy broth, and 40 g/liter glycerol at pH 6.4. Bacterial cells grew on the agar plate during the incubation, while the pigment spread into the agar plate, meaning that it is water soluble. Pigment production was affected by the initial cell density. Namely, at higher initial cell densities ranging from 106.3to 108.2CFU/cm2on the agar plate, faster pigment production was observed, but no blue pigment was produced at a very high initial density of 109.1CFU/cm2. Thus, the cell population of 108.2CFU/cm2was used for subsequent study. Although the bacterium was capable of growing at temperatures above and below 10°C, it could produce the pigment only at temperatures of ≥10°C. Moreover, the pigment production was faster at higher temperatures in the range of 10 to 20°C. Pigment production at various temperature patterns was well described by a new logistic model. These results suggested that the bacterium could be used in the development of a microbial temperature indicator for the low-temperature-storage management of foods and clinical materials. To our knowledge, there is no otherP. agglomeransstrain capable of producing a blue pigment and the pigment is a new one of microbial origin.


2019 ◽  
Vol 82 ◽  
pp. 497-503 ◽  
Author(s):  
Nadia Andrea Andreani ◽  
Lisa Carraro ◽  
Lihong Zhang ◽  
Michiel Vos ◽  
Barbara Cardazzo

2019 ◽  
Author(s):  
Craig A. Schenck ◽  
Josh Westphal ◽  
Dhileepkumar Jayaraman ◽  
Kevin Garcia ◽  
Jiangqi Wen ◽  
...  

ABSTRACTL-Tyrosine (Tyr) is an aromatic amino acid synthesized de novo in plants and microbes downstream of the shikimate pathway. In plants, Tyr and a Tyr pathway intermediate, 4-hydroxyphenylpyruvate (HPP), are precursors to numerous specialized metabolites, which are crucial for plant and human health. Tyr is synthesized in the plastids by a TyrA family enzyme, arogenate dehydrogenase (ADH/TyrAa), which is feedback inhibited by Tyr. In addition to ADH enzymes, many legumes possess prephenate dehydrogenases (PDH/TyrAp), which are insensitive to Tyr and localized to the cytosol. Yet the role of PDH in legumes is currently unknown. This study isolated and characterized Tnt1-transposon mutants of MtPDH1 (pdh1) in Medicago truncatula to investigate PDH function. The pdh1 mutants lacked PDH transcript, PDH activity, and displayed little aberrant morphological phenotypes under standard growth conditions providing genetic evidence that MtPDH1 is responsible for the PDH activity detected in M. truncatula. Though plant PDH enzymes and activity have been specifically found in legumes, nodule number and nitrogenase activity of pdh1 mutants were not significantly reduced compared to wild-type (Wt) during symbiosis with nitrogen-fixing bacteria. Although Tyr levels were not significantly different between Wt and mutants under standard conditions, when carbon flux was increased by shikimate precursor feeding, mutants accumulated significantly less Tyr than Wt. These data suggest that MtPDH1 is involved in Tyr biosynthesis when the shikimate pathway is stimulated, and possibly linked to unidentified legume-specific specialized metabolism.


Author(s):  
K.M. Hones ◽  
P. Sheldon ◽  
B.G. Yacobi ◽  
A. Mason

There is increasing interest in growing epitaxial GaAs on Si substrates. Such a device structure would allow low-cost substrates to be used for high-efficiency cascade- junction solar cells. However, high-defect densities may result from the large lattice mismatch (∼4%) between the GaAs epilayer and the silicon substrate. These defects can act as nonradiative recombination centers that can degrade the optical and electrical properties of the epitaxially grown GaAs. For this reason, it is important to optimize epilayer growth conditions in order to minimize resulting dislocation densities. The purpose of this paper is to provide an indication of the quality of the epitaxially grown GaAs layers by using transmission electron microscopy (TEM) to examine dislocation type and density as a function of various growth conditions. In this study an intermediate Ge layer was used to avoid nucleation difficulties observed for GaAs growth directly on Si substrates. GaAs/Ge epilayers were grown by molecular beam epitaxy (MBE) on Si substrates in a manner similar to that described previously.


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