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8 protocols using d histidine

1

Biochemical Assay Protocol for Protein Analysis

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D-histidine, L-histidine, azocasein, propidium iodide (PI), and fluorescein isothiocyanate-concanavalin A (FITC-ConA) were purchased from Sigma-Aldrich (St. Louis, MO, USA). DNA polymerase PrimeScrip™ RT Reagent Kit and TB Green® Premix Ex Taq™ II were purchased from TaKaRa (Dalian, China), and the RNeasy MinElute Cleanup kit was procured from QIAGEN (Hilden, Germany). These chemicals and materials were used according to the manufacturers’ instructions. Other chemicals and reagents were of analytical grade and purchased from commercial sources unless specified otherwise.
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2

Amino Acid Synthesis and Characterization

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d-Alanine, d-Arginine, d-Asparticacid, d-Asparagine, d-Glutamicacid, d-Histidine, d-Isoleucine, d-Leucine, d-Lysine, d-Methionine, d-Phenylalanine, d-Proline, d-Serine, d-Threonine, d-Tryptophan, d-Tyrosine, d-Valine, KBr (spectral grade), bovine serum albumin (BSA), glutathione and 3,3′,5,5′-tetramethylbenzidine (TMB) were purchased from Sigma-Aldrich Chemical Co. (St. Louis, MO, USA). d-Cystine and d-Glutarnine were purchased from Aladdin Reagent Co, Ltd. (Shanghai, China). All other chemicals and reagents were of analytical grade. All aqueous solutions were prepared with Milli-Q water.
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3

Immortalized HaCaT Keratinocyte Culture and Amino Acid Enrichment

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Immortalized human HaCaT keratinocytes29 (link) of passages 35–41 (gift from Dr J. Wood, University of Dundee; origin – German Cancer Research Center (DKFZ), Heidelberg, Germany) were seeded in six-well cell culture plates (Corning Incorporated, Corning, NY, USA) in D-MEM/F-12 medium with GlutaMAX (Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 10% fetal bovine serum and 1% penicillin/streptomycin. Monolayer cultures were typically confluent after 48–72 hours. From days 15–21, culture media were supplemented with additional 1–5 mM of amino acids (l-lysine, l-histidine, or d-histidine; Sigma-Aldrich Co., St Louis, MO, USA). Cells were harvested and lysed with Laemmli buffer (Sigma-Aldrich Co.) on day 21.
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4

Synthesis of PBI Derivative (D-PBI)

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The chemical structure of the PBI derivative (D-PBI) is reported in Figure 1. It was obtained according to the procedure reported in the literature (Gershberg et al., 2015 (link)).
Milli-Q grade water was used to dissolve the PBI derivative and all the organic compounds (D-phenylalanine, L-phenylalanine, D-serine, D-histidine), used in this contribution, were purchased from Sigma-Aldrich and used as received.
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5

Analysis of Anaerobic Bacterium C. novyi

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All L-amino acids, D-amino acids (except D-histidine), purines, Valine analogs, Terbium chloride (212903), Maltose (M5895), Sodium phosphate dibasic (S7907), o-phthaldialdehyde (P0657), N-acetyl cysteine (A7250), Sodium tetraborate decahydrate (B3545), HPLC grade methanol (34860), 1-Propanol (34871), Trifluoroacetic acid (302031) and Mutanolysin enzyme (M9901) were purchased from Sigma. 2-Propanol (29113-95) was obtained from Nacalai Tesque. D-histidine (sc-255057) was purchased from SantaCruz Biotechnology. Acetonitrile (1.00317) and HCl (1.00029) were purchased from Merck. Percoll (17089109) was purchased from GE Healthcare. Oxyrase for broth was purchased from Oxyrase Inc and Sigma (SAE0013). BBL polypeptone peptone (211910), Dehydrated cooked meat media (226730), Brain heart infusion broth (BHI, 237500) and Reinforced Clostridial medium (RCM, 218081) were purchased from BD. Fetal bovine serum (S1810) was obtained from iDNA Biotechnology.
C. novyi-NT was a gift from the Kinzler-Vogelstein lab in John Hopkins University, USA.
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6

Preparation of Amino Acid Solutions

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D-methionine, D-tryptophan, D-leucine, D- or L-cysteine, D- or L-aspartic acid, D- or L-glutamic acid, D-alanine, D-threonine, D-valine, D-isoleucine, D-glutamine, D-phenylalanine, D-histidine, D-proline, D-lysine, D-arginine, and glycine (Sigma-Aldrich, St. Louis, MO, USA) were all prepared at a concentration of 40 mM, and D-tyrosine was prepared at a concentration of 0.8 mM due to its low solubility. Nisin powder (2.5% purity, Sigma-Aldrich, St. Louis, MO, USA) was dissolved in a solution at pH 2 to obtain a stock solution with a concentration of 1 g/L.
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7

Capillary Electrophoresis Separation of Amino Acids

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All reagents were of analytical grade. FMOC-Cl, β-CD, pentane, sodium tetraborate, sodium hydroxide, glycine, d-glutamic acid, d-histidine, d-threonine, l-alanine, l-arginine, l-asparagine, l-aspartic acid, l-cysteine, l-glutamic acid, l-glutamine, l-histidine, l-isoleucine, l-leucine, l-lysine, l-methionine, l-proline, l-serine, l-threonine, l-tryptophan, l-tyrosine and l-valine, dl-alanine, dl-arginine, dl-asparagine, dl-aspartic acid, dl-cysteine, dl-glutamic acid, dl-histidine, dl-isoleucine, dl-leucine, dl-lysine, dl-phenylalanine, dl-proline, dl-serine, dl-tryptophan, and dl-valine were from Sigma-Aldrich (Steinheim, Germany). Isopropanol, dl-methionine, dl-tyrosine, sodium dodecyl sulfate, and acetonitrile were supplied by Fluka (Steinheim, Germany). Water was deionized and purified with a Milli-Q purification system (Millipore, Belford, NJ, USA).
The optimal BGE was 40 mM sodium tetraborate (adjusted to pH 9.5 with 1 M sodium hydroxide) containing 15% (v/v) isopropanol, 30 mM sodium dodecyl sulfate (SDS), and 30 mM β-CD. The BGE was filtered prior to use through 0.45-μm pore size disposable nylon filters from VWR (Amsterdam, The Netherlands). Stock solutions (3 mM) of AAs were prepared in 0.2 M sodium tetraborate (pH 9.5).
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8

Hierarchical Chiral ZIF-8 Synthesis

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For the synthesis of hierarchical macroporous chiral ZIF-8, zinc sulfate heptahydrate (ZnSO 4 .7H 2 O: 99%, Sigma-Aldrich), 2-methyl imidazolate (2-mIm; 99%, Sigma-Aldrich), L-histidine (99%, Sigma-Aldrich) and D-histidine (99%, Sigma-Aldrich) were used as metal center, original ligand and chiral ligand, respectively. Styrene monomer (TCI), potassium peroxide (KPS), ethyl acetate (Sigma-Aldrich) and ethanol (98%, Sigma-Aldrich) were used for the polystyrene bead synthesis. All chemicals were used without further purification.
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