Spontaneous precipitation of CaCO3 polymorphs in the presence of selected amino acids (AA) has been investigated. The L-aspartic acid (Asp), L-lysine (Lys), L-asparagine (Asn), L-tyrosine (Tyr), Lphenylalanine (Phe), L-serine (Ser) and L-alanine (Ala) were selected because of different charge and polarity of their side chains at applied experimental conditions. The investigated AA are building units of soluble macromolecules, putatively responsible for biomineralization of molluscs' exoskeletons. It was assumed that not only the acidic, but also the polar (hydrogen bonding) AA might contribute to macromolecules' interactions with the mineral surfaces. The mineralogical composition, structure and morphology of precipitates formed in the presence of wide range of concentrations of AA have been determined by XRD, FT-IR and EPR spectroscopy, HPLC-MS and SEM. In the reference system, without AA addition, a mixture of typical calcite rhombohedral crystals and vaterite spherulites has been observed, while AA with negatively charged or polar side chains (Asp, Tyr, Lys, Asn, Ser) significantly changed the morphology, phase composition and crystal structure of the precipitates. The effects of nonpolar AA (Phe, Ala) on the structural and morphological properties of precipitates are less pronounced. The stronger impact observed for polar AA and particularly negatively charged Asp, may be correlated with the additional electrostatic interactions of side-chain groups with mineral surfaces. Response to Reviewers: REVIEWER #1 This work investigates the effect of polar, charged and nonpolar amino acids, as well as their increasing concentrations, on the precipitation of calcium carbonate at high supersaturation. The authors explore a wide range of concentrations of soluble additives and also uses a systematic approach to evaluate the effects of several amino acids. However, this is not the first study to have used this exact same approach to we believe that the specific comments given in this report actually refer to the Langmuir version (indeed, in this report the Reviewer even used the previous title: "The Role of Amino Acids as Simple Models of Soluble Macromolecules Relevant for Calcium Carbonate Biomineralization"). Nevertheless, we addressed in this response all points, regardless they have been changed and accepted previously.
Silver nanoparticles (AgNPs) are the most exploited nanomaterial in agriculture and food production, and their release into the environment raises concern about their impact on plants. Since AgNPs are prone to biotransformation, various surface coatings are used to enhance their stability, which may modulate AgNP-imposed toxic effects. In this study, the impact of AgNPs stabilized with different coatings (citrate, polyvinylpyrrolidone (PVP), and cetyltrimethylammonium bromide (CTAB)) and AgNO3 on photosynthesis of tobacco plants as well as AgNP stability in exposure medium have been investigated. Obtained results revealed that AgNP-citrate induced the least effects on chlorophyll a fluorescence parameters and pigment content, which could be ascribed to their fast agglomeration in the exposure medium and consequently weak uptake. The impact of AgNP-PVP and AgNP-CTAB was more severe, inducing a deterioration of photosynthetic activity along with reduced pigment content and alterations in chloroplast ultrastructure, which could be correlated to their higher stability, elevated Ag accumulation, and surface charge. In conclusion, intrinsic properties of AgNP coatings affect their stability and bioavailability in the biological medium, thereby indirectly contributing changes in the photosynthetic apparatus. Moreover, AgNP treatments exhibited more severe inhibitory effects compared to AgNO3, which indicates that the impact on photosynthesis is dependent on the form of Ag.
Boc-L-DOPA(OBn) 2 -OH is a simple synthetic molecule that promotes hydrogelation through electrostatic and π−π stacking interactions. Hydrogelation can occur in alkaline conditions by the use of triggers. Four hydrogels were prepared varying the base, NaOH or Na 2 CO 3 , and the trigger, GdL or CaCl 2 . When the hydrogel formed in the presence of Na 2 CO 3 and CaCl 2 , the concomitant production of CaCO 3 crystals occurred, generating an organic/inorganic composite material. It was observed that the hydrogel once selfassembled preserved its status even if the trigger, the calcium ions, was removed. The viscoelastic behavior of the hydrogels was analyzed through rheological experiments, which showed a solid-like behavior of the hydrogels. The corresponding xerogels were analyzed mainly by scanning electron microscopy (SEM) and synchrotron X-ray diffraction analysis (XRD). They showed differences in structure, morphology, and fiber organization according to their source. This research presents a hydrogel system that can be applied as a soft biomaterial for tissue engineering, cosmetics, food, and environmental science. Moreover, it represents a model for biomineralization studies in which the hydrogel structure can act as an analogue of the insoluble matrix that confines the calcification site, provides Ca 2+ , and preserves its structure.
In many living organisms, biomolecules interact favorably with various surfaces of calcium carbonate. In this work, we have considered the interactions of aspartate (Asp) derivatives, as models of complex biomolecules, with calcite. Using kinetic growth experiments, we have investigated the inhibition of calcite growth by Asp, Asp2 and Asp3.This entailed the determination of a step-pinning growth regime as well as the evaluation of the adsorption constants and binding free energies for the three species to calcite crystals. These latter values are compared to free energy profiles obtained from fully atomistic molecular dynamics simulations. When using a flat (104) calcite surface in the models, the measured trend of binding energies is poorly reproduced. However, a more realistic model comprised of a surface with an island containing edges and corners, yields binding energies that compare very well with experiments. Surprisingly, we find that most binding modes involve the positively charged, ammonium group. Moreover, while attachment of the negatively charged carboxylate groups is also frequently observed, it is always balanced by the aqueous solvation of an equal or greater number of carboxylates. These effects are observed on all calcite features including edges and corners, the latter being associated with dominant affinities to Asp derivatives. As these features are also precisely the active sites for crystal growth, the experimental and theoretical results point strongly to a growth inhibition mechanism whereby these sites become blocked, preventing further attachment of dissolved ions and halting further growth. File list (2) download file view on ChemRxiv ASP-230919-Manuscript.pdf (773.33 KiB) download file view on ChemRxiv ASP-230919-SI.pdf (1.78 MiB)
As nanoparticles have been found to cause a range of harmful impacts in biota, understanding processes and transformations which may stabilize and increase their persistence time in the environment are of great importance. As nanoparticles carried in riverine or wastewaters will eventually reach estuaries, understanding their behavior and transport potential in this transition zone from fresh to marine waters is essential, particularly as estuaries are sensitive ecological zones, oftentimes encompassing ornithologically important areas. In this direction, we report on the influence of combined gradients of riverine and marine natural organic matter (NOM) on the temporal stability of biocorona-encapsulated silver nanoparticles in terms of ion release kinetics. In parallel, salinity, pH and oxygen saturation were simultaneously varied to create a model to mimic the complex estuarine environment. While humic acid (HA) and alginate (Alg) disrupted the stabilizing ability of the nanoparticle protein corona to a greater and lesser degree, respectively, they slowed the rate of ion release in freshwater at pH 6.6 and in saltwater at pH 8, respectively, while oxygen saturation was also found to be an important factor. Thus, as the type of NOM changes with pH along a salinity gradient in an estuary, conditions required to increase the persistence time of nanoparticles are serendipitously met, with greater colloidal stability achieved in cases where there is more rapid replacement of HA with Alg. Despite the strong gradients in ionic strength, pH and oxygen saturation, the protein corona was not sufficiently disrupted at the nanoparticle surface to be substituted by NOM indicating the greater adsorption energy of the protein’s hydrophobic domains. Ultimately, it is the specific NOM profile of individual estuaries that may provide the best indicator for predicting the stability and persistence of silver nanoparticles as they transition from fresh to salt water environments.
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