CHIMERIC THERMOSTABLE AMINOACYL-TRNA SYNTHETASE FOR ENHANCED UNNATURAL AMINO ACID INCORPORATION RELATED APPLICATIONS [0001] This application claims the benefit under 35 U.S.C. § 119(e) of U.S. Provisional Application No. 62/973,599, filed on October 15, 2019, which is incorporated herein by reference in its entirety. GOVERNMENT SUPPORT [0002] The current technology was developed using funds supplied by the National Institutes of Health (NIH) under grant Nos: R01GM126220, R01GM124319 and NIH/NIGMS R35 GM136437. Accordingly, the U.S. Government has certain rights to this invention. SEQUENCE LISTING [0003] The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on October 15, 2020, is named 0342_0009WO1_SL.txt and is 87,778 bytes in size. [0004] FIELD OF THE INVENTION [0005] The present invention is directed to the field of biotechnology, focusing on developing efficient platforms for expressing proteins site-specifically incorporating unnatural amino acids. BACKGROUND OF THE INVENTION [0006] Site-specific incorporation of unnatural amino acids (Uaas) holds much potential to probe and engineer the biology of mammalian cells. Central to this technology is an aminoacyl-tRNA synthetase (aaRS)/tRNA pair, which is engineered to charge the Uaa of interest in response to a nonsense or a frameshift codon, without cross-reacting with any of its host counterparts. Such “orthogonal” aaRS/tRNA pairs are typically imported into the host cell from a different domain of life. Thus, incorporation of Uaas in eukaryotic cells is mainly dependent on aaRS/tRNA pairs derived from bacteria. [0007] So far, three different bacterial aaRS/tRNA pairs have been used for Uaa incorporation in eukaryotes – ones charging tyrosine, leucine, and tryptophan – all derived from E. coli. The E. coli tyrosyl-tRNA synthetase (EcTyrRS)/tRNA pair was the first pair that was successfully engineered to incorporate Uaas in eukaryotes nearly two decades ago. Yet, the number of Uaa-selective mutants that has been generated using this pair remains very limited. In contrast, an archaea-derived tyrosyl pair, which has a similar active site architecture to EcTyrRS, has been successfully engineered to charge over 100 Uaas with high selectivity and efficiency. However, the archaea-derived tyrosyl pair cannot be used in eukaryotes, as it cross-reacts with its eukaryotic counterpart. The ability to further engineer the bacterial TyrRS/tRNA pair to accept a wider variety of Uaas will be extremely valuable for numerous applications related to probing and engineering protein structure and function in eukaryotic cells. [0008] It has been previously observed that introducing mutations into a protein’s active site to alter its activity is often associated with a decrease in the stability of its tertiary and quaternary structure. It is hypothesized that the outstanding success in engineering the archaeal TyrRS can be explained by its high structural stability, which ensures that a large set of its engineered mutants are still viable at physiological temperature in spite of suffering a drop in overall stability. In contrast, the EcTyrRS exhibits significantly lower thermostability. Consequently, destabilization associated with engineered mutations can more readily lead to proteins that are not viable at the physiological temperature. Such catastrophic loss of stability prevents access to EcTyrRS mutants that can potentially charge a wider assortment of structurally novel Uaas. The ability to develop a more thermostable bacterial TyrRS would overcome this limitation and will provide access to more extensively engineered mutants that charge structurally disparate Uaas. The same concept can be extended to all bacteria-derived aaRS mutants that are or can be engineered for Uaa incorporation in eukaryotic cells. SUMMARY OF THE INVENTION [0009] As used herein, the term "and/or" includes any and all combinations of one or more of the associated listed items. Further, the singular forms and the articles "a", "an" and "the" are intended to include the plural forms as well, unless expressly stated otherwise. It will be further understood that the terms: includes, comprises, including and/or comprising, when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. [0010] The present invention establishes a new strategy to generate chimeric aminoacyl-tRNA synthetase/tRNA pairs derived from bacteria that demonstrate high thermostability, as well as activity, and can be more aggressively engineered to generate mutants that can activate a broader selection of Uaas. Also described herein are compositions, such as the composition of chimeric TyrRS, derived from bacteria which are more stable, active and engineerable than their wild-type counterparts. [0011] Further, the present invention describes a method to generate chimeric bacterial aminoacyl-tRNA synthetase (aaRS) that exhibit enhanced thermostability as well as optimal biological activity to aminoacylate/charge tRNA with unnatural amino acids (also referred to herein as a non-canonical amino acid or ncAA)). Briefly, the methods claimed herein comprise the following steps. First, aaRS homologs from various thermophilic (e.g., Geobacillus stearothermophilus) and mesophilic bacteria (e.g., E. coli) are evaluated to characterize/identify their activity and thermostability. Next, a series of chimeras are generated by hybridizing the sequences of a thermostable aaRS and its homolog that has high aminoacyl enzymatic activity. The chimeras are characterized to identify ones that exhibit higher thermostability as well as optimal biological activity, wherein the biological activity can be defined as the ability to aminoacylate tRNA. Also described herein are compositions of such chimeric bacterial TyrRSs (ChTyrRS), derived from E. coli TyrRS (EcTyrRS) and Geobacillus stearothermophilus TyrRS (GsTyrRS). The ChTyrRS show higher thermostability than EcTyrRS and higher activity than both GsTyrRS and EcTyrRS. ChTyrRSs tolerate Uaa-selective mutants better than EcTyrRS, affording higher solubility and activity relative to their wild-type counterparts. Thus, the ChTyrRS compositions described are more engineerable and useful for genetic code expansion (GCE). [0012] In particular, the present invention encompasses compositions comprising a chimeric thermostable aminoacyl-tRNA synthetase derived from a nucleic acid sequence of a bacterial thermostable aminoacyl-tRNA synthetase hybridized to a nucleic acid sequence of its mesophilic bacterial aminoacyl-tRNA synthetase homolog. Thermostable microorganisms typically grow in the range of about 50 degrees C to about 70-80 degrees centigrade. Mesophilic microorganisms typically grow in more physiological conditions at about 20 degrees centigrade to about 45 degrees centigrade. [0013] A wide variety of thermal stable bacteria are known to those of skill in the art and can include, for example, Geobacillus stearothermophilis, Bacillus stearothermophilis, Thermus thermophilis or a Thermoanaerobacter species. Many mesophilic bacteria are also known to those skilled in the art and can include, for example, Escherichia coli, any Staphylococcus species, any Streptococcus species, or any Pseudomonas species. A particular embodiment of the present invention comprises a chimera wherein the relevant portion of the nucleic acid sequence of the thermostable bacteria is Geobacillus stearothermophilis is hybridized to the relevant portion of the nucleic acid sequence of the mesophilic bacteria is Escherichia coli. Selection of the relevant portion of the nucleic acid sequences of the individual components of the chimeric bacteria is determined as described herein using techniques known to those of skill in the art. [0014] The chimeric compositions described herein also encompass chimeras comprising a mesophilic bacterial aminoacyl-tRNA synthetase (aaRS) that can be genetically engineered to incorporate one, or more, mutations/variations in its active site, resulting in the alteration of the substrate specificity of the aminoacyl-tRNA synthetase relative to the wild-type aminoacyl-tRNA synthetase (also referred to herein as variant chimeric thermostable aminoacyl-tRNA synthetases). These mutations/variations result in the ability of the aaRS to charge corresponding/cognate tRNAs with unnatural amino acids. The aaRS can be genetically engineered with the selected mutations prior to linkage/hybridization with the thermal stable aaRS. Alternatively. the aaRS can be engineered to incorporate an active site mutation after hybridization/linkage to its thermostable counterpart. The cognate tRNA can be the wild-type tRNA or can be genetically engineered to improve its activity as described in International Application No.: PCT/US2020/038766, the teachings of which are incorporated herein by reference. Importantly, as described herein, the chimeric aminoacyl-tRNA synthetases of the present invention exhibit increased thermostability relative to its individual wild-type mesophilic bacterial progenitor aaRS and higher biological activity (e.g., enhanced structural stability and/or increased solubility at physiological temperatures e.g., up to about 60°C, or increased ability to aminoacylate its cognate tRNA) relative to its individual wild-type thermophilic progenitor aaRS. Thus, the chimeras of the present invention have optimal thermostability and biological activity relative to their wild-type progenitor aminoacyl- tRNA synthetases to incorporate unnatural amino acids into mammalian proteins. [0015] As described herein, the chimeric thermostable aminoacyl-tRNA synthetase of the present invention will have increased thermal stability relative to the mesophilic wild- type bacterial aaRS. The biological activity of the chimeric thermostable bacterial mesophilic aaRS can be defined as activity to aminoacylate/charge its cognate wild-type or variant tRNA with any of the known naturally occurring amino acids, or, if the chimera is a variant chimera, the activity to aminoacylate/charge its cognate tRNA with an unnatural amino acid. [0016] The chimeric aminoacyl-tRNA synthetase variants of the present invention can have increased biological activity over the wild-type aminoacyl-tRNA synthetase to aminoacylate/charge its cognate wild-type or variant tRNA with an unnatural amino acid. Unnatural amino acids (Uaas) are known to those of skill in the art and can include analogs/derivatives of any of the naturally occurring amino acids. Some examples of Uaas of the present invention can include phenylalanine analogs such as p-benzoylphenylalanine (pBpA); tyrosine analogs such as O-methyltyrosine (OMeY); tryptophanyl analogs (5- azidotryptophan, 5-propargyloxytryptophan, 5-aminotryptophan, 5-methoxytryptophan, 5- O-allyltryptophan, or 5-bromotryptophan) or lysyl analogs. These analogs can be purchased from commercial sources (e.g., www.chemimpex.com) or synthesized by one of skill in the art using known methods (also see, for example, U.S. Patent No. 10/717,975, the teachings of which are incorporated herein in their entirety). [0017] A particular embodiment of the present invention is a composition of a chimera that comprises thermostable bacterial aminoacyl-tRNA synthetase GsTyrRS and the mesophilic bacterial aminoacyl-tRNA synthetase EcTyrRS. More specifically, a chimeric composition of the present invention (referred to herein as Ch2TyrRS-WT or ChTyrRS- H2) comprises the nucleic acid sequence which comprises SEQ ID NO:1, SEQ ID NO:41, or a nucleic acid sequence with at least 80% sequence identity to Seq ID NO: 1 or SEQ ID NO:41. or a nucleic acid sequence comprising about 80%, 85%, 86%, 87%, 88%, 89% 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO:1 or SEQ ID NO:41. The amino acid sequence corresponding the this chimers is found in Figure 15 as SEQ ID NO:42. [0018] Alternatively, the chimeric composition (referred to herein as Ch6TyrRS-WT or ChTyrRS-H6) comprises the chimeric nucleic acid sequence SEQ ID NO:2, SEQ ID NO:45, or a nucleic acid sequence about 80%, 85%, 86%, 87%, 88%, 89% 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO:2 or SEQ ID NO:45. The corresponding amino acid sequence is found in Figure 15 as SEQ ID NO:46. [0019] It is to be understood that all of the nucleic acid sequences and amino acid sequences described herein include corresponding sequences comprising about 80%, 85%, 86%, 87%, 88%, 89% 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to the specific SEQ ID NO specifically named. [0020] Further encompassed are variant chimeric thermostable aminoacyl-tRNA synthetases with mutations in the active site, for example, wherein the mutation in the active site results in the enzymatic activity for incorporation of an unnatural amino acid in a mammalian protein. In one embodiment the Uaa is a phenylalanine analog. In a particular embodiment the phenylalanine analog is p-benzoylphenylalanine (pBpA). [0021] More particularly, the amino acid sequence of a chimeric thermostable aaRS that incorporates pBpA into a mammalian protein is referred to herein as Ch2TyrRS-pBpA and comprises SEQ ID NO; 43 (with mutations in the active site Y37G, D179G, L183A), or an amino acid sequence with at least 80%, 85%, 86%, 87%, 88%, 89% 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO:43. [0022] Alternatively, the amino acid sequence of a chimeric thermostable aaRS that incorporates pBpA into a mammalian protein is referred to herein as Ch6TyrRS-pBpA and comprises SEQ ID NO: 47 (with mutations in the active site Y37G, D182G, L186A), or an amino acid sequence with at least 80%, 85%, 86%, 87%, 88%, 89% 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO:46. [0023] Also encompassed herein is an aaRS, wherein the mutation in the active site results in the incorporation of a tyrosine analog into a mammalian protein. More specifically, the tyrosine analog can be O-methyltyrosine (OMeY). The amino acid sequence of a chimeric thermostable aaRS that incorporates OMeY into a mammalian protein is referred to herein as Ch2TyrRS-poly and comprises SEQ ID NO:44 (with active site mutations Y37V, D176S, F180M, L183A), or an amino acid sequence with at least 80%, 85%, 86%, 87%, 88%, 89% 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO:44. [0024] Also encompassed by the present invention are cells (either cultured in vitro or in vivo) comprising a chimeric aaRS of the present invention. Such cells can also comprise the chimeric aaRS’s cognate tRNA. Such cells can further comprise all cellular components required for translation of polynucleotides into proteins, including translation system components such as, for example, ribosomes, endogenous tRNAs, translation enzymes, mRNA and amino acids, resulting in the ability to produce proteins with naturally-occurring or unnatural amino acids incorporated therein. [0025] The cells of the present invention can be any bacterial cell or eukaryotic cell suitable for use with the chimeric thermostable aaRS/tRNA, or chimeric thermostable aaRS variant/tRNA pairs described herein. For example, the cell can be selected from the group consisting of a yeast cell, insect cell or a mammalian cell. In particular, the bacterial cell is a genetically-engineered E. coli cell, or a homologous/analogous bacterial cell. More specifically, the E. coli is the ATMY series of strains as described herein. [0026] Also encompassed by the present invention are methods of producing a chimeric thermostable aminoacyl-tRNA synthetase. The first step is to identify the suitable aaRS enzyme sequences to be linked as a chimera. For example, one skilled in the art can identify/evaluate an aminoacyl-tRNA synthetase of interest in a mesophilic microorganism (e.g., bacteria such as E. coli). The next step is to identify/evaluate a suitable aaRS homolog from a thermophilic microorganism with increased thermostability relative to the mesophilic microorganism aminoacyl-tRNA synthetase thermostability as described herein. [0027] Once the suitable aaRS sequences are identified and characterized the chimera comprising the relevant sequences of the thermostable aminoacyl-tRNA synthetase and the mesophilic aminoacyl-tRNA synthetase can be constructed as described herein. The chimera can then be evaluated for thermostability and biological activity to aminoacylate/charge its cognate tRNA relative to its wild type progenitor aminoacyl-tRNA synthetases. [0028] More specifically, as described herein, the technique of DNA shuffling was used to produce the chimeras of the present invention. DNA shuffling involves the digestion of a gene or homologous genes into random fragments, and the reassembly of those fragments into a full-length gene by PCR. The reassembled gene sequences are them evaluated/tested for thermophilic and enzymatic activity. [0029] In a particular embodiment described herein, the mesophilic aaRS can be engineered to aminoacylate unnatural amino acid analogs, forming a variant chimeric thermostable aaRS with the enzymatic activity to charge/aminoacylate its cognate tRNA with the unnatural amino acid analog. The Uaa can be a phenylalanine analog, specifically, the phenylalanine analog is p-benzoylphenylalanine (pBpA). Alternatively, the Uaa is a tyrosine analog. More specifically, the tyrosine analog can be O-methyltyrosine (OMeY). Additional tyrosine analogs are known to those skilled in the art and can include, for example, sulpho-tyrosine, iodo-tyrosine, chloro-tyrosine and nitro-benzyl-tyrosine. [0030] Also encompassed herein are methods of producing a protein in a cell with one, or more, unnatural amino acids at specified positions in the protein. The method comprises the following steps: [0031] a. culturing the cell in a culture medium under conditions suitable for growth, wherein the cell comprises a nucleic acid that encodes a protein with one, or more, amber or opal selector codons, wherein the cell further comprises an Ec-tRNA ^UAA that recognizes the selector codon(s), and wherein the cell further comprises a chimeric thermostable aminoacyl-tRNA synthetase that preferentially aminoacylates the Ec-tRNA ^UAA with an unnatural amino acid; [0032] b. contacting the cell culture medium with one, or more, unnatural amino acid analogs corresponding to the Uaa of the Ec-tRNA ^UAA under conditions suitable for incorporation of the one, or more, unnatural amino acids into the protein in response to the selector codon(s), thereby producing the protein with one, or more unnatural amino acids at specified positions of the protein. [0033] In particular, the methods can comprise any of the chimera thermostable aminoacyl-tRNA synthetases described herein. In particular, the chimera can comprise the nucleic acid sequence SEQ ID NO:1 or SEQ ID NO:41, or a nucleic acid sequence with at least 80% sequence identity to SEQ ID NO: 1 or SEQ ID NO:41, or the nucleic acid sequence SEQ ID NO:2 or SEQ ID NO:45, or a nucleic acid sequence with at least 80% sequence identity to SEQ ID NO: 2, or SEQ ID NO:45. [0034] In one embodiment, the unnatural amino acid to be incorporated into the protein is p-benzoylphenylalanine (pBpA) and the chimera is Ch2TryRS-pBpA or Ch6TryRS- pBpA, wherein the amino acid sequence of the Ch2TryRS-pBpA chimera comprises SEQ ID NO:43 or SEQ ID NO: 47, or an amino acid sequence with at least 80% sequence identity to either SEQ ID NO: 43 or SEQ ID NO:47. [0035] In another embodiment, the unnatural amino acid to be incorporated into the protein is unnatural amino acid O-methyltyrosine (OMeY) and the chimera is Ch2TyrRS- poly, wherein the Ch2TyrRS-poly chimera comprises SEQ ID NO:44, or an amino acid sequence with at least 80% sequence identity to either SEQ ID NO:44. [0036] The cell can be an E. coli cell or a eukaryotic cell. In one embodiment the eukaryotic cell is a mammalian cell. In another embodiment, the E. coli is an ATMY E. coil strain. [0037] Further, the present invention covers kits for producing a protein in a cell, wherein the protein comprises one, or more Uaa incorporate into the protein. For example, wherein the protein comprises one, or more pBpA residues, the kit comprises a container containing a polynucleotide sequence encoding an Ec-tRNA ^pbpa that recognizes an amber or opal selector codon(s) in a nucleic acid of interest in the cell; and a container containing a polynucleotide sequence encoding the chimeric thermostable aminoacyl-tRNA synthetase Ch2TryRS-pBpA or Ch6TyrRS-pBpA. [0038] The polynucleotide encoding the chimera encodes the amino acid sequence of the chimera comprising SEQ ID NO:43 or SEQ ID NO:47, or an amino acid sequence with at least 80% sequence identity to either SEQ ID NO:43 or SEQ ID NO:47. The kit can further comprise one, or more, p-benzoylphenylalanine molecules. and instructions for producing the protein. [0039] Alternatively, the kit can be used for producing a protein in a cell, wherein the protein comprises one, or more O-methyltyrosine (OMeY) residues. The kit can include a container containing a polynucleotide sequence encoding an Ec-tRNA ^poly that recognizes an amber or opal selector codon(s) in a nucleic acid of interest in the cell, and a container containing a polynucleotide sequence encoding the chimeric thermostable aminoacyl- tRNA synthetase Ch2TyrRS-poly. [0040] The polynucleotide encoding the chimera encodes the amino acid sequence SEQ. ID. NO:44, or an amino acid sequence comprising at least 80% sequence identity to SEQ ID NO:44. The kit can further comprise one, or more, O-methyltyrosine (OMeY) molecules, and instructions for producing the protein. [0041] The current invention demonstrates features and advantages that will become apparent to one of ordinary skill in the art upon reading the following Description of the Drawings and Detailed Description. BRIEF DESCRIPTION OF THE DRAWINGS [0042] In the accompanying drawings, reference characters refer to the same parts throughout the different views. The drawings are not necessarily to scale; emphasis has instead been placed upon illustrating the principles of the invention. The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawings(s) will be provided by the Office upon request and payment of the necessary fee. Of the drawings: [0043] Figures 1A-1C show that engineered TyrRS mutants show lower thermostability. A) EcTyrRS active site, showing bound tyrosine in magenta, and highlighting mutated residues in engineered variants (shown below). B) Western blot analysis of soluble and insoluble fractions of E. coli cell free extract expressing EcTyrRS- WT and EcTyrRS-pBpA reveals that the latter is largely insoluble. C) Thermal shift assay of various TyrRS variants. Dot-blot was performed (using an anti-polyhistidine antibody) on the soluble fraction of E. coli cell-free extracts expressing the indicated TyrRS variants (left), after incubation at the indicated temperature (top). [0044] Figures 2A-2C show that bacterial TyrRS chimeras created from GsTyrRS and EcTyrRS exhibit higher activity and intermediate thermostability. A) Two chimeras, Ch2TyrRS and Ch6TyrRS, created by fusing EcTyrRS (green) and GsTyrRS (magenta) sequences. The EcTyrRS crystal structure was used to highlight the progenitor sequences in the two chimeras. B) Thermal shift assay of the two chimeras, as well as their wild-type progenitors, in E. coli cell-free extract. Dot-blot was performed (using an anti-polyhistidine antibody) on the soluble fraction of E. coli cell-free extracts expressing the indicated TyrRS variants (left), after incubation at the indicated temperature (top). C) Activity of the TyrRS variants in ATMY E. coli strains, measured using the expression of sfGFP-151TAG reporter in the presence of tRNACUA ^Tyr . Characteristic fluorescence of the full-length sfGFP-151-TAG reporter was measured in resuspended cells. [0045] Figures 3A-3B show that chimeric TyrRS variants better tolerate pBpA- selective mutations. A) Thermal shift assay of the pBpA selective TyrRS mutants constructed from the two wild-type or chimeric scaffolds, in E. coli cell-free extract. Dot- blot was performed (using an anti-polyhistidine antibody) on the soluble fraction of E. coli cell-free extracts expressing the indicated TyrRS-pBpA variants (left), after incubation at the indicated temperature (top). B) Activity of the TyrRS-pBpA variants in the ATMY E. coli strain, measured using the expression of sfGFP-151TAG reporter in the presence of tRNACUA ^Tyr and in the presence and absence of 1 mM pBpA. Characteristic fluorescence of the full-length sfGFP-151-TAG reporter was measured in resuspended cells. [0046] Figures 4A-4C. Figures 4A and 4B show that chimeric TyrRS derived mutants exhibit improved activity for ncAA incorporation in mammalian cells. A) TyrRS-pBpA variants were co-expressed in HEK293T cells with tRNA _CUA ^Tyr and EGFP-39-TAG, in the presence and absence of pBpA, and the expression of the full-length reporter was monitored by its characteristic fluorescence in cell-free extract. The expression level was reported as the % of an identical experiment where wild-type EGFP reporter (no TAG) was used as the reporter. B) The ncAA-incorporation efficiency of Ch2TyrRS-Poly is comparable to the highly active EcTyrRS-Poly. Activity was measured as described in section (A) in the presence and absence of 1 mM OMeY. See Figure 9 for all associated fluorescence images. Figure 4C shows that the ChTyrRS-pBpA show enhanced activity relative to either wild-type counterparts. Activity was measured by expressing a GFP-151- TAG reporter in E. coli cells in the presence of tRNA-EcTyr (TAG suppressor). [0047] Figure 5 shows the nucleic acid sequences of ChTyrRS-H2 (SEQ ID NO:1) and ChTyrRS-H6 (SEQ ID NO:2). [0048] Figure 6 shows that the activity of EcTyrRS-pBpA is significantly weaker than EcTyrRS-WT. Activity was evaluated using the sfGFP-151-TAG reporter, expressed in ATMY E. coli, by measuring the characteristic fluorescence of the full-length reporter in resuspended cells. For EcTyrRS-pBpA, the expression was measured in the presence or absence of 1 mM pBpA. [0049] Figure 7 shows the MjTyrRS mutants used in this study. The active site structure of MjTyrRS is also shown highlighting the key residues mutated to generate non- canonical amino acids (ncAA or Uaa)-selective variants. [0050] Figure 8 shows the sequence alignment of EcTyrRS-WT (SEQ ID NO: 29) and GsTyrRS-WT (SEQ ID NO: 30) and its consensus sequence. [0051] Figure 9 shows the fluorescence images of mammalian cells expressing EGFP- 39-TAG reporter using various TyrRS/tRNA pairs (shown above), in the presence or absence of relevant ncAAs (left). These images correspond to the fluorescence values presented in Figure 4. [0052] Figure 10 shows SDS-PAGE analysis of the EGFP-39-pBpA reporter expressed in HEK293T cells using Ch2TyrRS-pBpA. [0053] Figures 11A-B show the deconvoluted ESI-MS analysis of EGFP-39-pBpA reporter expressed in HEK293T cells using Ch2TyrRS-pBpA. Two different magnifications of the same spectra are shown. The major species (29771 Da) corresponds to the expected mass; 29729 Da peak likely represents the same species lacking N-terminal acetylation (- 42 Da), while 29787 Da peak likely arises from oxidation (+16 Da). [0054] The text of the final plasmid maps and sequences are provided below with the following color coding: aaRS highlighted red, antibiotic selectable marker highlighted blue, tRNA highlighted purple, lacI highlighted green, and the origin of replication highlighted orange. The images are not color coded. [0055] Figure 12 shows the plasmid map and sequences of pBK MCS GsYRS WT and where the active site mutations are located in Ch2TyrRS-pBpA variant, and also where the active site mutations are located in the Ch6TyrRS-pBpA variant. (SEQ ID NOS 31, 1 and 2), respectively, in order of appearance). [0056] Figure 13 shows the plasmid map and sequences of pET22b 10X N-term His GsYRS (SEQ ID NOS 32-36, respectively, in order of appearance). [0057] Figure 14 shows the plasmid map and sequences of pBIU Gs-BPA-RS and where the active site mutations are located in the Ch2YyrRS-OMeY variant. (SEQ ID NOS 37-40, respectively, in order of appearance). [0058] Figure 15 shows the following sequences in order of appearance: [0059] Ch2TyrRS-WT nucleotide sequence (SEQ ID NO: 41) and its encoded amino acid sequence (SEQ ID NO: 42). [0060] Ch2TyrRS-pBpA amino acid SEQ ID NO: 43. Mutations are highlighted in red: Y37G, D179G, L183A. [0061] Ch2TyrRS-poly amino acid SEQ ID NO: 44. Mutations are highlighted in red; Y37V, D176S, F180M, L183A. [0062] Ch6TyrRS-WT nucleotide sequence (SEQ ID NO: 45) and its encoded amino acid sequence (SEQ ID NO: 46). [0063] Ch6TyrRS-pBpA amino acid SEQ ID NO: 47. Mutations are highlighted in red: Y37G, D182G, L186A. [0064] DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS [0065] While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims. [0066] Non-canonical amino acid (ncAA) mutagenesis of proteins in living cells has emerged as a powerful technology with enormous potential. ^1-5 A ncAA of interest can be co-translationally incorporated using an orthogonal aminoacyl-tRNA synthetase (aaRS)/tRNA pair in response to a nonsense or frameshift codon. ^1-5 Central to this technology is the ability to engineer the substrate specificity of a natural aaRS through directed evolution. Many useful ncAAs have been genetically encoded in E. coli using the Methanocaldococcus jannaschii derived tyrosyl-tRNA synthetase (MjTyrRS)/tRNA pair, including those containing bioconjugation handles, photo-affinity probes, biophysical probes, models for natural post-translational modification, etc. ^{1, 2, 5} While some of these functionalities can also be genetically encoded using other aaRS/tRNA pairs, several others (e.g., those modeling natural post-translational modifications) are reliant on the unique architecture of the TyrRS active site. ^{1, 2, 5} Unfortunately, however, this enabling toolset cannot be used in eukaryotic cells, as the archaea-derived MjTyrRS/tRNA pair cross-reacts with its eukaryotic counterpart. Typically, bacteria-derived aaRS/tRNA pairs are suitable for ncAA incorporation in eukaryotes, as they tend to be orthogonal in these cells. ^{1, 3, 5-7} Indeed, the E. coli derived tyrosyl-tRNA synthetase (EcTyrRS)/tRNA pair has been established for ncAA incorporation in eukaryotic cells. ^8-12 It was first engineered to incorporate ncAAs into proteins expressed in eukaryotic cells nearly two decades ago. Yet, the ncAA-toolbox developed using this pair remains surprisingly limited, particularly when compared to the remarkable success of the MjTyrRS/tRNA pair during the same time period. ^{1-3, 5, 13} The ability to recapitulate the success of the MjTyrRS/tRNA platform using a bacterial TyrRS/tRNA pair will significantly expand the scope of the genetic code expansion (GCE) technology in eukaryotes by providing access to structurally unique ncAAs that are challenging to genetically encode using alternative aaRS/tRNA pairs. [0067] The limited success of the EcTyrRS/tRNA pair can be, at least partially, attributed to the challenges associated with the directed evolution platform used to alter its substrate specificity. ^{1, 3, 7, 13} Unlike MjTyrRS, which can be readily engineered using a facile E. coli based directed evolution system, a more cumbersome yeast-based selection scheme is needed to engineer EcTyrRS. ⁸ To address this challenge, a novel strategy was developed that involves the development of unique E. coli strains (ATMY strains), where the endogenous EcTyrRS/tRNA pair is functionally substituted with an archaeal counterpart. ^{1, 3, 7, 13} (see also U.S. Patent No. 10/717975). It was demonstrated that such strains can be generated without incurring a significant growth penalty. ¹³ The ‘liberated’ EcTyrRS/tRNA pair can be subsequently established in the resulting ATMY strains as an orthogonal nonsense suppressor. This has enabled the use of the facile E. coli based directed evolution platform to engineer the substrate specificity of EcTyrRS. ¹³ [0068] Although the ability to rapidly engineer the EcTyrRS/tRNA pair using this facile directed evolution platform has provided access to several new ncAAs, in some instances, the resulting engineered mutants demonstrated poor activity. For example, it was attempted to develop an EcTyrRS mutant that efficiently charges p-benzoylphenylalanine (pBpA), a powerful photoaffinity probe that has been useful for capturing weak and transient molecular interactions. ^{8, 14-17} Even though EcTyrRS was previously engineered using the yeast-based selection platform to selectively charge pBpA, the utility of this mutant has been limited due to its weak activity. When a large EcTyrRS active site mutant library was subjected to the facile selection system, the same mutant was identified that was previously developed by selection in yeast. This indicated that the observed set of mutations indeed optimally recodes the EcTyrRS active site for charging pBpA. The activity of this pBpA-selective EcTyrRS was somewhat low, as measured in the ATMY E. coli strain using the sfGFP-151-TAG reporter (Figure 6). A systematic investigation identified that the EcTyrRS-pBpA mutant was largely insoluble in E. coli, potentially explaining its poor activity (Figure 1B). Western blot analysis of the soluble and insoluble fractions of cell-free extracts of E. coli expressing polyhistidine-tagged EcTyrRS-WT and EcTyrRS-pBpA revealed that the latter is nearly exclusively found in the insoluble fraction (Figure 1B). In contrast, a large portion of the wild-type EcTyrRS was found in the soluble fraction. [0069] It has been previously observed that when a protein is subjected to directed evolution to attain an altered function, the stability of the resulting mutants is often compromised. ^18-21 Consequently, the extent to which a protein can be engineered is often limited by how stable it is. It was hypothesized that the success in engineering MjTyrRS, an enzyme derived from a thermophilic archaeon, is likely facilitated by its high structural stability. In contrast, EcTyrRS, derived from mesophilic bacteria, may be a less stable scaffold and have a lower tolerance for active site mutations. To test this notion, a modified cellular thermal shift assay (CETSA) was utilized. ^{22, 23} In this assay, cell-free extract expressing a target protein is heated to increasing temperatures, and the amount of remaining protein in the soluble fraction is subsequently tested by immunoblotting. The temperature range at which a protein is lost from the soluble fraction provides an estimate of its thermostability. In addition to EcTyrRS-WT and EcTyrRS-pBpA, a polyspecific EcTyrRS mutant (EcTyrRS-Poly)was also tested that is highly active (Figure 1A). For comparison, MjTyrRS-WT was include, as well as two of its comparable engineered mutants: one selective for pBpA (MjTyrRS-pBpA), ²⁴ and another that exhibits ncAA polyspecificity (MjTyrRS-Poly) (Figure 7). ²⁵ All of these proteins encoded an N-terminal hexahistidine tag (SEQ ID NO: 3) to facilitate their detection in a dot-blot assay using an anti-polyhistidine antibody. As expected, MjTyrRS was found to be highly thermostable, maintaining solubility up to 80 °C (Figure 1C). In contrast, EcTyrRS was much less stable, and was lost from the soluble fraction between 50 °C and 60 °C (Figure 1C). These values are consistent with previously reported thermostability measurements. ²⁶ All of the engineered mutants exhibited reduced stability relative to their wild-type counterparts. MjTyrRS-pBpA mutant was slightly less stable than its polyspecific counterpart, but both were soluble at physiological temperature. In contrast, for EcTyrRS, only the polyspecific mutant was soluble at physiological temperature; the pBpA selective mutant was not detected in the soluble fraction even at the lowest temperature tested (Figure 1C). These observations support the hypothesis that the lower stability of EcTyrRS negatively impacts its engineerability. While some of its active site mutants, such as EcTyrRS-Poly, are adequately stable and active under physiological conditions, more destabilizing mutants such as EcTyrRS-pBpA are not viable. [0070] To overcome this challenge, the possibility of adapting a TyrRS from a thermophilic bacterium was considered, which might offer a higher degree of engineerability relative to EcTyrRS. Several aminoacyl-tRNA synthetases derived from the thermophilic bacterium Geobacillus stearothermophilus have been purified and structurally characterized. ^27-29 TyrRS from this bacterium (GsTyrRS) is homologous to EcTyrRS (Figure 8) but is significantly more thermostable, offering an attractive scaffold for engineering ncAA-selective mutants. ²⁶ The stability and the activity of GsTyrRS was tested using the CETSA and the sfGFP-151-TAG expression assay, as described above (Figure 2B). GsTyrRS was indeed significantly more stable than EcTyrRS, but its activity was somewhat lower in E. coli (Figures 2B, 2C). It was previously investigated whether enzymes derived from thermophilic bacteria exhibit weaker activity at lower temperature. ³⁰ [0071] A chimera from EcTyrRS and GsTyrRS was then constructed that exhibited an optimal balance of stability and activity. It has been previously shown that such chimeric enzymes can be excellent scaffolds for protein engineering. ^{31, 32} As described herein, the technique of DNA shuffling was used to produce the chimeras of the present invention. Briefly, DNA shuffling involves the digestion of a gene or homologous genes into random fragments, and the reassembly of those fragments into a full-length gene by PCR. The gene fragments prime on each other based on sequence homology, and recombination occurs when fragments from one copy of a gene anneal to fragments from another copy, causing a template switch, or crossover event. As described herein, naturally occurring homologous genes such as aminoacyl-tRNA synthetases from mesophilic and thermophilic microorganisms are used as the progenitor sources for the hybrids. The gene(s) are digested/cut into random segments with appropriate restriction enzymes to fragments of about 100 to 300 base pairs long. The segments are then reassembled by using a suitable a DNA polymerase with overlapping segments or by using some version of overlap PCR (see for example, Sheryl B. Rubin-Pitel, et.al., in Bioprocessing for Value-Added Products from Renewable Resources, 2007; H. Kamada, S.-I. Tsunoda, in Biomaterials for Cancer Therapeutics, 2013; David P. Clark, Nanette J. Pazdernik, in Biotechnology (Second Edition), 2016). The resulting constructs can then be sequenced and evaluated for the desired characteristics using known protocols. [0072] Several chimeras were constructed and tested between EcTyrRS and GsTyrRS and two were identified, Ch2TyrRS and Ch6TyrRS (Figure 2A), which show higher levels of activity (Figure 2C) and intermediate thermostability (Figure 2B) relative to their wild- type progenitors, when expressed in ATMY E. coli. Next, pBpA-selective mutants of these TyrRS variants were generated and tested. Both Ch2TyrRS-pBpA and Ch6TyrRS-pBpA were more thermostable than EcTyrRS-pBpA and were also soluble at physiological temperature (Figure 3A). This was reflected by the significantly higher degree of activity observed for these enzymes (Figure 3B). Interestingly, even though GsTyrRS was the most thermostable, the corresponding pBpA-selective mutant was found to be largely insoluble and poorly active when expressed in E. coli (Figure 3A, 3B). While the basis of this observation is unclear, it indicates that the chimeras may be better suited for engineering new ncAA-selective variants. [0073] The activity of these engineered pairs was evaluated in the ATMY E. coli strain, where it is significantly easier to control parameters affecting the assay performance, such as the expression level of the aaRS/tRNA pairs. To demonstrate the utility of these new tools in eukaryotic cells, the activity of the pBpA-selective TyrRS variants were tested in HEK293T cells. EcTyrRS-pBpA, GsTyrRS-pBpA, Ch2TyrRS- pBpA, and Ch6TyrRS-pBpA were each cloned into a mammalian expression vector under a UbiC promoter, which also encodes 16 copies of the tRNA ^Tyr _CUA expression cassette. The resulting plasmids were co-transfected into HEK293T cells with another plasmid encoding an EGFP-39-TAG reporter, and the full-length reporter expression was monitored in the presence or absence of 1 mM pBpA in the media (Figure 4A, and Figure 9). Expression of a wild-type EGFP reporter (no in-frame TAG codon) was also included as a control. All four TyrRS-pBpA variants enabled successful incorporation of pBpA into the reporter. However, Ch2TyrRS-pBpA and Ch6TyrRS-pBpA demonstrated significantly higher activity (up to 36% of wild-type EGFP) relative to EcTyrRS-pBpA and GsTyrRS-pBpA (Figure 4A). The reporter protein expressed using Ch2TyrRS-pBpA was isolated using Ni- NTA affinity chromatography and characterized by SDS-PAGE (Figure 10) and mass- spectrometry analysis (Figures 11A-B) to confirm successful pBpA incorporation. It is worth noting that the activity of GsTyrRS-pBpA in mammalian cells was found to be significantly higher than what is expected from its assessment in ATMY E. coli, where it was found to be nearly inactive. It is possible that the more sophisticated protein folding machinery of the mammalian cells is able to better process unstable engineered proteins like GsTyrRS-pBpA. The TyrRS variants are also expressed more strongly in mammalian cells than in E. coli, which may also contribute to the observed difference. [0074] Nonetheless, these results demonstrate that the chimeric TyrRS variants provide improved platforms for the GCE technology in eukaryotes. To further highlight the generality of this approach, Ch2TyrRS-Poly was constructed by introducing previously reported active site mutations for generating EcTyrRS-Poly (Figure 1A), an engineered mutant that charges several different ncAAs including O-methyltyrosine (OMeY). When tested in HEK293T cells, both EcTyrRS-Poly and Ch2TyrRS-Poly exhibited comparable activity for EGFP-39-TAG reporter expression (Figure 4B and Figure 9), confirming that the chimeric TyrRS is able to recapitulate the activity of well-behaved bacterial engineered EcTyrRS mutants, while providing a better scaffold for those with suboptimal stability. [0075] Work in the last two decades have provided a deep insight into how the biophysical properties of a protein influence its evolution. ^18-21 It is now clear that the function-altering mutations acquired during experimental or natural evolution can often negatively impact the structural stability of a protein. The work described herein highlights its impact on the GCE technology, which relies on engineered aaRSs that selectively charge ncAAs of interest. The structural robustness of MjTyrRS has been shown and has contributed to its remarkable success as a powerful GCE platform. In contrast, the lower stability of EcTyrRS compromises the extent to which its active site can be altered. It is important to note that the same limitation likely affects the engineerability of several other aaRS/tRNA pairs, derived from mesophilic organisms (e.g., E. coli or yeast), ^{3, 6, 33-35} which have been adapted for ncAA incorporation. Indeed, the success of engineering these platforms for ncAA incorporation has been limited. As a result of the work described herein, a strategy to overcome this challenge by taking advantage of more thermostable aaRS homologs derived from thermophilic organisms is now available. [0076] The chimeras generated from thermophilic and mesophilic aaRS homologs may be even better suited for this purpose. Analogous strategies have been used to create optimal starting points for the directed evolution of enzymes such as cytochrome P450. ³¹ It is possible that instead of simple aaRS chimeras like the ones reported here, more sophisticated counterparts with even better properties can be created by constructing and selecting a DNA-shuffling library of EcTyrRS and GsTyrRS. Additionally, as shown herein, the relative performance of the same aaRS in different expression systems can be different. For example, the GsTyrRS-pBpA mutant, which is largely insoluble and inactive in E. coli, demonstrated robust activity in mammalian cells. This might stem from differences in protein folding machinery in different host cells, as well as other factors such as variable expression level of the aaRS, speed of translation, codon usage, etc. [0077] In summary, here is established the structural robustness of an aaRS as an important factor that significantly impacts its engineerability for GCE. A roadmap for creating more engineerable bacterial aaRS variants by hybridizing homologs from mesophilic and thermophilic bacteria is provided. Mutants generated from such chimeric TyrRSs show robust activity in both ATMY E. coli strain as well as in mammalian cells, suggesting that these are more attractive scaffolds for extensive engineering. Directed evolution of these using the facile ATMY E. coli based selection system should provide access to new enabling ncAAs. Finally, improved pBpA-incorporation activity of ChTyrRS-pBpA will further facilitate the application of this important photo-crosslinker ncAA for uncovering new biomolecular interactions in eukaryotic cells. [0078] Without further elaboration, it is believed that one skilled in the art can, based on the above description, utilize the present invention to its fullest extent. The following specific embodiments and examples are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever. [0079] Examples [0080] The following examples are provided to illustrate embodiments of the present invention but are by no means intended to limit its scope. The examples described herein will be understood by one of ordinary skill in the art as exemplary protocols. One of ordinary skill in the art will be able to modify these procedures appropriately and as necessary. [0081] Introduction [0082] The present invention describes the composition of thermostable bacteria- derived TyrRS variants that can be more aggressively engineered for Uaa incorporation than their wild-type counterparts. The invention is not restricted to TyrRS, however; the method to generate such active and thermostable mutants, which is described as a part of this invention, can also be readily extended to all other bacteria-derived aaRSs that can be engineered for Uaa incorporation in eukaryotic cells. [0083] The work described herein with E. coli derived TyrRS (EcTyrRS) has revealed that many of the engineered mutants that have already been developed show poor folding and stability in cells. Expression of these mutants followed by analysis of the soluble and insoluble fractions of the proteome by Western blot reveals the majority of the mutant proteins are insoluble. Further analysis using CETSA (Cellular Thermal Stability Assay) show that the EcTyrRS is not as thermostable as its archaea derived counterpart that has been successfully engineered to incorporate numerous Uaas in bacteria. Furthermore, it has been found that the mutants derived from the archaeal TyrRS are also less stable than their wild-type counterpart, but still sufficiently viable at the physiological temperature, highlighting the importance of having a thermostable wild-type aaRS for developing Uaa- selective mutants. [0084] To overcome the poor thermostability of EcTyrRS, a homologous TyrRS from the thermophilic bacteria Geobacillus stearothermophilus (GsTyrRS) was identified and evaluated. Although GsTyrRS was more stable, it exhibited significantly lower activity relative to EcTyrRS. This was not unexpected, as the stability and activity of enzymes are often negatively correlated. [0085] The present invention describes a method to generate chimeric aaRS mutants that demonstrate optimal balance between thermostability and activity. By generating a chimera between two homologous aaRS – one highly active but less stable, and the other highly stable (from a thermophile such as Geobacillus stearothermophilus) – it is possible to create chimeras that exhibit such optimal properties. For example, by generating chimeras between EcTyrRS and GsTyrRS, novel sequences have been generated that are still significantly more stable than EcTyrRS yet have higher activity in both bacterial and eukaryotic cells. Such chimeras can be generated either by rational fusion of homologous stretches, or by DNA shuffling of the thermostable and the active aaRS sequences. [0086] The method described in this invention for creating stable yet active bacterial aaRS variants is not restricted to any one particular aaRS. The same strategy can be applied to generate optimal chimeric variants of any other bacterial aaRS including, but not limited to, those charging alanine, glycine, serine, cysteine, methionine, tryptophan, phenylalanine, leucine, isoleucine, valine, proline, threonine, selenocysteine, lysine, arginine, asparagine, glutamine, glutamic acid, aspartic acid, and histidine. [0087] The chimeric aaRS variants generated by this method can be more aggressively engineered to create mutants that selectively charge various Uaas. Due to their improved robustness, these would provide access to a wider range of Uaa-selective mutants. In addition to unnatural amino acids, the aaRS mutants can also be used to charge other nonnatural substrates including, but not limited to, hydroxyl-acids, thio-acids, β-amino acids, etc. [0088] These engineered aaRS mutants can be used in any eukaryotic cell along with the appropriate cognate tRNA (suppressing a nonsense or frameshift codon, or a codon composed of one or more nonnatural nucleobases). Such expression hosts include, but are not limited to, yeast, insect cells, and mammalian cells. Additionally, these aaRS/tRNA pairs can also be used for Uaa incorporation in engineered ATM E. coli strains, where this bacterial pair has been functionally replaced with a eukaryotic or archaeal counterpart. The present invention describes the composition of thermostable bacteria-derived TyrRS variants that can be more aggressively engineered for Uaa incorporation than their wild- type counterparts. The invention is not restricted to TyrRS, however; the method to generate such active and thermostable mutants, which is described as a part of this invention, can also be readily extended to all other bacteria-derived aaRSs that can be engineered for Uaa incorporation in eukaryotic cells. [0089] Example 1: [0090] Materials and methods [0091] General materials: [0092] All cloning and plasmid propagation were done in DH10B E. coli cells. Restriction enzymes, Phusion HS II High-Fidelity DNA polymerase, and IPTG were obtained from Fisher. T4 DNA ligase was obtained from Enzymatic. DNA extraction and PCR clean up were conducted with Macherey-Nagel Binding Buffer NTI and Epoch mini spin columns from Thermo Fisher Scientific. Media components were obtained from Fisher Scientific. The following antibiotic stock concentrations were used: ampicillin 100 μg/mL, kanamycin 50 μg/mL, spectinomycin 100 μg/mL, chloramphenicol 35 μg/mL for LB Agar plates and cultures. A Cole Parmer Ultrasonic Processor was used for making E. coli lysate by sonication. Protein purification was conducted with a HisPur Ni-NTA resin from ThermoScientific. Dot blots were done with GE Healthcare life sciences nitrocellulose blotting membrane (0.45 um). Western blots were conducted with a PVDF membrane, antibodies, and SuperSignal West Dura Extended Duration Substrate for western blot from Thermo Fisher Scientific. [0093] Accession codes: [0094] E. coli tyrosyl-tRNA synthetase (EcTyrRS, NCBI BAA15398.2) [0095] G. stearothermophilus tyrosyl-tRNA synthetase (GsTyrRS, NCBI KOR92528.1) [0096] Bacterial and virus strains [0097] Chemicals, peptides, and recombinant proteins [0098] Experimental models: cell lines [0099] Construction of plasmids to express aaRS for ncAA incorporation into sfGFP and EGFP: The G. stearothermophilus tyrosyl-aaRS was PCR amplified from a gBlock purchased from IDT, digested with NdeI/NcoI, and inserted into the pBK vector backbone. The mutant G. stearothermophilus tyrosyl-aaRS mutants were then generated via standard site-directed mutagenesis of the appropriate active site residues. The pBK E. coli tyrosyl-aaRS wild type and mutants were previously reported. ^36,37 [00100] The chimeric H2 and H6 aaRS’ were constructed by PCR amplification of the E. coli tyrosyl-aaRS N-terminus and the G. stearothermophilus C-terminus. The inserts were then made through overlap amplification, digested with NdeI/NcoI, and inserted into the pBK vector backbone. The mutant chimeric aaRS were then generated via standard site-directed mutagenesis. ³⁸ [00101] For expression of the aaRS in mammalian cells, terminal primers were used to PCR amplify the aaRS’ from their respective pBK plasmids. This was followed by digestion of the PCR products with NheI/XhoI into the pB1U vector backbone. [00102] Construction of plasmids to express aaRS for CETSA: The E. coli, G. stearothermophilus, and chimeric aaRS’ were PCR amplified from their respective pBK constructs, digested with NdeI/HindIII, and inserted into the pET22b vector backbone. The N-terminal primer appended a 10X-Histidine tag (SEQ ID NO: 4) to each aaRS for future imaging. [00103] sfGFP* fluorescence analysis and expression: For E. coli expression, the pBK aaRS and pEvol T5 EcY-TAG sfGFP151* reporter plasmids were co-transformed into ATMY6 cells. ³⁶ A 5 mL overnight culture was inoculated with a single colony and the appropriate antibiotics. The overnight starter culture was then used to inoculate a 20 mL LB Media culture supplemented with antibiotics. Cultures were grown to an OD600 of 0.6 then induced with a final concentration of 1 mM IPTG, the appropriate ncAA (1 mM), and incubated for 16 hours at 30 ºC with shaking (250 rpm). The cultures were then spun down, the LB media was removed, and the cells were resuspended in 1X PBS. Fluorescence readings were collected in a 96-well plate using a SpectraMAX M5 (Molecular Devices) (ex= 488 nm and em=534 nm). Mean of two independent experiments were reported, and error bars represent standard deviation. [00104] EGFP* fluorescence analysis, expression and purification: For fluorescence analysis, HEK 293T cells were seeded at a density of 600,000 cells per well for a 12-well plate the day before transfection. A total amount of 1.5 μg DNA (0.75 μg of each plasmid for two-plasmids) + 3.5 μL PEI + 17.5 μL DMEM was used for transfection of each well. Fluorescence images and EGFP expression analysis were performed 48 hours post transfection following previously mentioned protocols. ³⁹ Fluorescence readings were collected in a 96-well plate using a SpectraMAX M5 (Molecular Devices) (ex= 488 nm and em=510 nm). Mean of four independent experiments were reported, and error bars represent standard deviation. [00105] For EGFP protein purification incorporating one ncAA, HEK293T cells were seeded in 100 mm cell culture dishes (5 million per dish) 24 hours prior to transfection. [00106] CETSA assay: For aaRS expression, TOP10 E. coli cells were transformed with a single pET22b-N-terminal-10X-Histidine tagged-aaRS plasmid. Overnight cultures were inoculated with a single colony, then used to inoculate 20 mL LB Media cultures with the appropriate antibiotics, grown to an OD600 of 0.6, and induced with IPTG (final concentration of 1 mM) for 15 minutes at 30 ºC with shaking. The cultures were then spun down, the LB Media was removed, and the cell pellets were resuspended in 500 μL of sonication buffer (100 mM NaCl, 25 mM Tris HCl, pH 8.0). [00107] For lysate preparation, the cell pellets were treated to three freeze thaw cycles followed by three cycles of sonication (75% power, 20 pulses), spun down, and the supernatant was collected. Each supernatant was divided into 50 μL aliquots and heated at varying temperatures for 5 minutes on a Perkin Elmer Cetus DNA Thermal Cycler 480 and spun down at maximum speed for 10 minutes. Then 3 μL of the supernatant was inoculated on a nitrocellulose membrane and treated to western blot analysis following previously described protocols. ³⁹ Antibodies used for imaging include: mouse anti-Histidine 6X tag (SEQ ID NO: 3) antibody (1:1000 dilution), chicken anti-mouse IgG secondary antibody- HRP conjugate (1:5000 dilution). [00108] Solubility Western: DH10B cells were transformed with a pET22b-N-term- 10X-His-aaRS plasmid and an overnight 5 mL culture was inoculated with a starter colony. A 20 mL culture was then inoculated and grown to an OD600 of 0.6, allowed to grow for 4 hours at 30 ºC, spun down, and lysed by sonication following the same protocol as the aforementioned CETSA assay. This was resolved using 12% SDS-PAGE gel and worked up for a western following previously described protocols. ⁴ The antibodies used for this protocol were the same as those for the CETSA assay. [00109] Primers and other DNA sequences: [00110] EcYRS NdeI-F [00111] TTTGAGGAATCCCATATGGCAAGCAGTAACTTGATTAAACAATTGCA AGAG (SEQ ID NO: 5) [00112] EcYRS NcoI-R [00113] AATTCCATGGTTATTTCCAGCAAATCAGACACTAATTC (SEQ ID NO: 6) [00114] GsYRS NdeI-F [00115] ATTATTATGAATCCCATATGATGGACCTGCTGGCGGAACTGCAATG (SEQ ID NO: 7) [00116] pBK MCS JI sq-R [00117] GAGATCATGTAGGCCTGATAAGCGTAGC (SEQ ID NO: 8) [00118] H2 EcYRS-iR [00119] GCGATCGGACGGTGACCCGCCTGCTGGAAGCGTTTCAGGCATAACA ATG (SEQ ID NO: 9) [00120] H2 GsYRS-iF [00121] CCTGAAACGCTTCCAGCAGGCGGGTCACCGTCCGATCGCGCTGGTTG (SEQ ID NO: 10) [00122] H6 EcYRS-iR [00123] CCGCTTTCGGTTTTGCCAAATTTGGTGCCATCTGCTTTAGTGATCAGC GGAACG (SEQ ID NO: 11) [00124] H6 GsYRS-iF [00125] CACTAAAGCAGATGGCACCAAATTTGGCAAAACCGAAAGCGGTACC ATTTG (SEQ ID NO: 12) [00126] EcYRS NheI-F [00127] TTTGAGGAATCCGCTAGCGCAAGCAGTAACTTGATTAAACAATTGCA AGAG (SEQ ID NO: 13) [00128] EcYRS XhoI-R [00129] AATTCTCGAGTTATTTCCAGCAAATCAGACACTAATTC (SEQ ID NO: 14) [00130] GsYRS NheI-F [00131] ( Q ) [00132] GsYRS XhoI-R [00133] AATTCTCGAGTTACGCATAACGAATCAGATAGTATTTC (SEQ ID NO: 16) [00134] EcYRS-nterm10XHis-NdeI-F [00135] GAAATTACATATGCATCATCACCATCACCATCATCATCATCACGCAA ( Q ) [00136] EcYRS-HindIII-R [00137] 18) [00138] GsYRS-nterm10XHis-NdeI-F [00139] GAAATTACATATGCATCATCACCATCACCATCATCATCATCACGACC ( Q ) [00140] GsYRS-HindIII-R [00141] ( Q : 20) [00142] MjYRS-nterm10XHis-NdeI-F [00143] ttgaaatgataaagagaaacacatctg (SEQ ID NO: 21) [00144] MjYRS-HindIII-R [00145] NO: 22) [00146] GeobacYRS-Y34G-R [00147] GC CCGCGG CGGG CG CCGC CCC GGG C C CG CC [00148] GeobacYRS-D176G-R [00149] ( ) [00150] GeobacYRS-GGFL-L180A-R TG (SEQ ID NO: 25) [00151] GeobacYRS-D176G-F [00152] [00153] GeobacYRS-GGFL-L180A-F CAAGCGTATGGTTTCCTGCGTGCCTACGAAACCGAAGGCTGCCGTCT G (SEQ ID NO: 27) [00154] gBlock sequence of G. stearothermophilus tyrosyl aminoacyl-tRNA synthetase [00155] [00156] Example 2: [00157] Construction of Tyrosyl-tRNA synthetase chimeric libraries through DNA shuffling: [00158] The G. stearothermophilus and E. coli TyrRS are PCR amplified using external primers that anneal ~70 bp upstream and downstream of the target sequence. The amplified target genes are gel-purified, mixed in equimolar ratio, and were partially digested with DNASe I. The fragmented inserts were gel purified and reassembled following an established stepwise amplification protocol. ⁴⁰ The reassembled product was then PCR amplified with a second set of primers that anneal ~40 bp upstream and downstream of the target sequence, and cloned into a plasmid behind a constitutively active promoter. [00159] Construction of Tyrosyl-tRNA synthetase chimeric libraries through StEP: [00160] The G. stearothermophilus and E. coli TyrRS are PCR amplified using external primers that anneal ~70 bp upstream and downstream of the target sequence. The amplified target genes were gel-purified, mixed at an equimolar ratio, and PCR amplified with Taq- polymerase for 80 cycles (short low-temperature cycles, such as 5 s at 55 °C) with a second set of primers that anneal ~40 bp upstream and downstream of the target sequence. ⁴¹ During this amplification, short stretches of the sequences are generated, which can reanneal to a different template in the following cycle, resulting in chimeric constructs. The resulting chimeric constructs were cloned into a plasmid behind a constitutively active promoter. [00161] Construction and selection of aaRS-GFPmut3 fusion fluorescence reporter construct: [00162] The library of chimeric TyrRS mutants are first selected for activity. This selection uses the ability of the active TyrRS mutants to enable the expression of a TAG- inactivated antibiotic resistance gene (such as ampicillin or chloramphenicol) and allow the host survive the corresponding antibiotic treatment. Next, the library of active chimeric TyrRS mutants was PCR amplified and fused with a GFP reporter (e.g., the GFPmut3 reporter) using overlap-extension PCR. The full-length fusion insert ⁴² was cloned into a plasmid under a strong and inducible promoter such as T5-lac. The resulting plasmid library is then transformed into E. coli cells and the chimeric proteins are expressed. Those with lower stability would render the fused GFP non-fluorescent, while the stable variants will keep the GFP fluorescent. A FACS selection is then used to enrich the most stable and active mutants. Isolated mutants are individually screened for both their stability and activity. [00163] REFERENCES: [00164] The following references are herein incorporated by reference in their entirety. [00165] [1] Chin, J. W. (2017) Expanding and reprogramming the genetic code, Nature 550, 53. [00166] [2] Dumas, A., Lercher, L., Spicer, C. D., and Davis, B. G. 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[00207] While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims.