Chemo-Biocascade Reactions Enabled by Metal–Organic Framework Micro-Nanoreactor

The one-pot combination of biocatalytic and chemocatalytic reactions represents an economically and ecologically attractive concept in the emerging cascade processes for manufacturing. The mutual incompatibility of biocatalysis and chemocatalysis, however, usually causes the deactivation of catalysts, the mismatching of reaction dynamic, and further challenges their integration into concurrent chemo-biocascades. Herein, we have developed a convenient strategy to construct versatile functional metal–organic framework micro-nanoreactors (MOF–MNRs), which can realize not only the encapsulation and protection of biocatalysts but also the controllable transmission of substances and the mutual communication of the incompatible chemo-biosystems. Importantly, the MOFs serving as the shell of MNRs have the capability of enriching the chemocatalysts on the surface and improving the activity of the chemocatalysts to sufficiently match the optimum aqueous reaction system of biocatalysts, which greatly increase the efficiency in the combined concurrent chemo-biocatalysis. Such strategy of constructing MOF–MNRs provides a unique platform for connecting the “two worlds” of chemocatalysis and biocatalysis.


Introduction
In the long course of the evolution, enzymes with features of high activity and substrate specificity have developed to perform a wide range of catalytic functions, and their cascade reactions in the cell provide a research basis for revealing the rule of biological activities [1]. Learning from nature, researchers have been pursuing the integration of two or more types of catalysts in vitro at the micro-and nanoscale levels for designing highly efficient hybrid catalysts [2]. While achieving their biological functions in multienzyme catalytic cascades [3][4][5], enzymes can, when compatible with chemocatalysts, possess high activity and enantioselectivity under certain conditions [6,7]. In comparison to the enzyme cascades, chemocatalysts with a range of new advantages may enrich the enzymes' repertoire, such as good stability, various substrate choices, and diverse reaction types [8]. However, the reaction conditions of biocatalysts are usually different from those of the chemocatalysts in that the two types of catalysts are frequently deactivated in the one-pot reaction process [6]. Generally speaking, some biocatalysts (enzymes) prefer the aqueous phase reaction system at relatively low temperature [9,10], whereas the chemocatalysts favor the organic phase at high temperature [11]. Also, the matching between chemical catalysts' and biocatalysts' activity is also a challenging issue [12,13]. Therefore, how to achieve compatibility between the two catalysts becomes a major concern in the one-pot integration of biocatalysis and chemocatalysis.
As early as 1980, Makkee et al. [14] reported the first chemo-biocatalysis cascade system in two separated reaction units. They used heterogeneous metal catalysts to achieve hydrogenation reaction and then combined with enzymes to implement isomerization reaction. At that time, the conversion of D-glucose to D-mannitol not only promoted the development of sugar manufacturing but also provided a new method for combining chemo-and biocatalysts to achieve unique chemical conversion. However, the two-step cascade system faced problems of low efficiency, separation, and purification, which motivated the researchers to develop a one-pot cascade system. Generally, there are three ways to realize the one-pot chemo-biocatalysis efficiently. First is improving the activity of the chemocatalysts under the condition of enzyme reaction. Li et al. synthesized lipasepalladium (Pd) nanohybrids by using single lipase-polymer nanoconjugates as confined nanoreactors [15], in which the Pd nanoparticle (Pd NP) size was down to 0.8 nm. The 0.8 nm Pd NPs not only exhibited enhanced activity in racemization of (S)-1-phenylethylamine ((S)-1-PEA) but also matched efficient reaction dynamics of lipase at low temperature and aqueous solutions. Therefore, reducing the size of metal nanoparticles or introducing active supports in the enzyme reaction system can improve the efficiency of the overall cascade reaction. Second is enhancing the enzyme activity and stability through gene regulation or chemical modification [16]. A typical example is enhanced activation of laccase, and carbonic anhydrase was observed when Cu 3 (PO 4 ) 2 ·3H 2 O nanoflowers were incorporated into the enzyme solution [17]. The activity of the enzymes in Cu 3 (PO 4 ) 2 ·3H 2 O nanoflowers could largely expand the catalytic range and boost the efficiency of enzymes. Although the above two types of approaches have rendered the chemo-or biocatalysts compatibility to a certain extent, they still cannot completely avoid the mutual deactivation due to the direct contact between the two catalysts in the one-pot reaction system, achieving the compatibility and activity matching in the chemo-bioconcurrent system. Subsequently, the strategies of micro-nanoreactors (MNRs) were developed to realize the spatial separation of chemo-and biocatalysts to prevent mutual deactivation. Numerous materials like phospholipid bilayers [18], polymers [19], and mesoporous organosilicons [20] were assembled into MNRs, such as liposomes, polymersomes, and colloidosomes, for the encapsulation of chemo-or biocatalysts [21]. For instance, mesoporous core-shell structured nanocatalysts with PdPt bimetallic core and enzyme-immobilized polydopamine (PDA) shell were designed by Gao et al. [22]. The concept of integrating metals and enzymes at spatially distinct locations of core-shell materials has great potential in performing efficient one-pot cascade reactions. However, some major challenges remain in the field of concurrent chemobiocascades under the conditions of low temperatures and aqueous solution by MNR strategy: (1) to achieve selective transport of reaction substrates by shell of MNRs to adapt to more complex reaction system, (2) to improve the stability and activity of the enzyme, and (3) to enhance catalytic activity of the chemocatalysts that can match the enzymatic reactions at ambient conditions. Hence, the development of a suitable material for constructing MNRs becomes key to achieve efficient chemo-and biocatalysis in one-pot.
Metal-organic frameworks (MOFs) [23][24][25][26][27] are a kind of organic-inorganic hybrid porous materials with a periodic network structure, which are extensively used in gas storage [28][29][30][31], catalysis [32][33][34][35][36], separation [37], and medicine [38][39][40][41]. Due to adjustable pores and uniform pore sizes [42], MOFs as the shell of MNRs will not only enable the separation of chemo-and biocatalysts but also precisely regulate the transport of substances [13]. Moreover, the organic-inorganic hybrid system of MOFs with abundant physical-chemical microenvironment can regulate the catalytic activity of chemo-and biocatalysts [4,43]. Therefore, MOFs as the constructing units of MNRs may promise the concurrent chemo-biocascades. Herein, we develop a facile strategy to construct metal-organic framework micro-nanoreactors (MOF-MNRs) by self-assembling MOF particles on oil-water surface, which can realize efficient encapsulations for chemoor biocatalysts, selective transmission for substrates, enhanced activity for chemocatalysts, and mutual communications for incompatible chemo-biocatalysts in concurrent chemobiocascades ( Figure 1). In contrast to previous reports on MNRs constructed by other materials, MNRs with MOFs as the shell have achieved controllable communications of reaction substrates and size selectivity of the chemocatalysts, ensuring their efficiency in complex reaction environments. The chemical microenvironments of MOFs can enrich chemocatalysts and regulate their electronic status, further boosting their activity and adapting to the reaction condition of enzymes at a relatively low temperature and aqueous solution. Notably, the as-prepared hybrid chemo-biocatalysts (AlcDH/ NAD + @MOF-MNRs combined with Pt[(C 6 H 5 ) 3 P] 4 ) exhibit an improved efficiency as well as good enantioselectivity in concurrent chemo-biocatalysis.

Synthesis and Structure Characterization of MOF-MNRs.
To verify the capability of MOF-MNRs in concurrent chemo-biocascade catalysis, UiO-66-NH 2 , one kind of MOFs, is taken as an example to construct the MOF-MNRs mainly due to its stable frame structure and easy modification. The formation process of MOF-MNRs is demonstrated in Figure 2(a). UiO-66-NH 2 NPs are synthesized through the reaction among zirconium chloride (ZrCl 4 ), benzoic acid (C 7 H 6 O 2 ), and 2-aminoterephthalic acid (NH 2 -BDC) mixture in N, N-dimethylformamide (DMF) at 120°C for 24 h. The prepared UiO-66-NH 2 NPs are well dispersed and possess uniform size of~100 nm (Figure 2(b)). The postmodification of heptanoic anhydride is employed to regulate the hydrophobicity of UiO-66-NH 2 NPs, in which the acid anhydride bond of heptanoic anhydride is amidated with the exposed amino group on the NH 2 -BDC ligand and a heptanoic acid is grafted on the frameworks of UiO-66-NH 2 . In this way, the originally hydrophilic UiO-66-NH 2 NPs become hydrophobic ones (the contact angle is 122.5°) mainly because the alkyl chain of heptanoic acid substitutes the amino group of ligands ( Figure 2(c)). The size and morphology of UiO-66-NH 2 NPs reveal no obvious change after the hydrophobic modification. The increase of contact angle and the decrease in gravimetric Brunauer-Emmett-Teller (BET) surface areas of the hydrophobic UiO-66-NH 2 NPs further indicate the successful hydrophobic modification ( Figure S1), which facilitates the subsequent assembly of modified MOF NPs in water-in-oil Pickering emulsions. MOF-MNRs are fabricated by selfassembly of the hydrophobic UiO-66-NH 2 on water-oil interface, with polymer precipitation being used as the support layer for enhancing stability. The spherical MOF-

Research
MNRs with a dense MOF layer on the surface were about 10-20 μm in diameter (Figures 2(d) and 2(e)). MOF-MNRs presented similar crystal structure to the UiO-66-NH 2 NPs, as demonstrated by the X-ray diffraction (XRD) patterns ( Figure S2). Based on the above characterizations, it can be concluded that MOF particles are self-assembled on the surface of MNRs and form a dense shell. Therefore, MOF-MNRs not only own the MOF shell for potential selective transport of molecules but also possess a hollow cavity for possibly encapsulating chemo-or biocatalysts and providing reaction place ( Figure S3). MOF-MNRs can be acquired by self-assembly of the hydrophobic MOF NPs on water-oil interface, supported by a polymer layer to enhance stability. The dispersion of hydrophobic MOF NPs in the oil phase and the addition of the hydrophilic enzymes in the water phase can encapsulate the enzymes inside the MOF-MNRs through the self-assembly on Pickering emulsion interface, contributing to the spatial separation of chemo-and biocatalysts in one-pot cascade reactions. Here, a zinc-containing metalloenzyme (alcohol dehydrogenase (AlcDH)) with broad substrate specificity and its cofactors (nicotinamide adenine dinucleotide (NAD + )) is chosen to study the encapsulation process of enzymes. The show strong fluorescence intensity, corresponding to green light and red light, respectively, evidencing the existence of both AlcDH and NAD + in the MOF-MNRs. In order to confirm the location of enzyme in MOF-MNRs, the stepping method of scanning fluorescence process is employed, and the fluorescence intensity is observed from weak to strong and again to weak along the z-axis of MOF-MNRs ( Figure S4). The above results reflect the even distribution of enzyme in the three-dimensional space of the cavity, indicating that the enzymes are successfully encapsulated in MOF-MNRs.

Multifunctionality of MOF-MNRs.
Homogeneous metal catalysis combined with enzymes has historically dominated the chemical and pharmaceutical industries especially by the use of transitional metals as chemocatalyst components. The The overall reaction is driven by a "sacrifice reaction" of formate to carbon dioxide (CO 2 ), and then, through the mediation of NAD + and NADH, reactants can undergo asymmetric reactions to become target products. AlcDH: alcohol dehydrogenase; NAD + : nicotinamide adenine dinucleotide.
3 Research compatibility of both catalysts and reaction conditions becomes critical when simultaneously proceeding transition metals and enzyme reactions in concurrent chemobiocascades [6,[44][45][46]. Here, the compatible capability of the MOF-MNRs in concurrent chemo-biocatalysis is further demonstrated, through combination of the metal complex catalyst (tetrakis(triphenylphosphine)platinum (Pt[(C 6 H 5 ) 3 P] 4 )), the regeneration of the coenzyme NAD + with NADH-AlcDH reduction of pyruvic acid for synthesis of lactic acid (Figure 3(a)). And we adopt a widely applicable method to investigate the pyruvate reduction reaction at a certain amount of time by measuring the intensity of NADH [47]. It is well acknowledged that the reduction process cannot occur if there is only AlcDH or Pt[(C 6 H 5 ) 3 P] 4 serving as catalysts in the reaction system due to the reaction nature of concurrent chemo-biocatalysis ( Figure S5). When directly mixing the AlcDH and Pt[(C 6 H 5 ) 3 P] 4 in a reaction system, AlcDH will be deactivated (Figure 3(b)). The successful encapsulation of enzyme in MOF-MNRs makes compartmentalization of the chemo-and biocatalysts come true, and then, the catalysts consisting of AlcDH/NAD + @UiO-66-NH 2 -MNRs and Pt[(C 6 H 5 ) 3 P] 4 exhibit good conversion in the reduction of pyruvic acid to lactic acid at 40°C and 200 rpm in aqueous solution for 12 h. The results mainly contribute to that the uniform micropore size of UiO-66-NH 2 (pore size: 6 Å) [48] discourages the entrance of the Pt[(C 6 H 5 ) 3 P] 4 to contact with AlcDH. Furthermore, AlcDH/NAD + @UiO-66-NH 2 -MNRs show good recyclability in 3 cycles of concurrent cascade chemo-biocatalysis ( Figure S6). To further investigate the compartmentalization effect of MOF-MNR structure, the polymer (polymethyl methacrylate (PMMA)) micronanoreactors (PMMA-MNRs) are chosen as a comparison. PMMA-MNRs with spherical shapes are obtained by following the similar procedure expect that MOF NPs are replaced by Span 80 ( Figure S7). Although PMMA-MNRs can achieve the encapsulation of enzyme, AlcDH/   Research NAD + @PMMA-MNRs and Pt[(C 6 H 5 ) 3 P] 4 catalysts exhibit lower activity ( Figure S8), which is caused by the nonuniform meso/macropores in PMMA structure with no molecular sieving ability [42]. The diffusion comparison of MOF-MNRs and PMMA-MNRs clearly shows their differences in protecting biomolecules ( Figure S9). Besides encapsulating enzymes, our strategy can also encapsulate chemocatalysts using the oil-in-water Pickering emulsion system, and thus, space separation can be achieved. Although Pt[(C 6 H 5 ) 3 P] 4 @MOF-MNRs with AlcDH/NAD + demonstrate good conversion in the reduction of pyruvic acid to lactic acid when there are substances such as proteases in the system, the enzymes outside the cavity tend to be inactivated ( Figure S10). In addition, MOF-MNRs can effectively improve the stability of the encapsulated enzymes. AlcDH/NAD + @UiO-66-NH 2 -MNRs and pure AlcDH are dispersed in phosphate buffer at room temperature for several days, and the UV-vis spectra are employed to analyze the activity of the AlcDH. The enzyme activity was further evaluated after the reaction in the systems of pure AlcDH, AlcDH/NAD + @PMMA-MNRs, and AlcDH/NAD + @MOF-MNRs. The intensity of special peak in 260~278 nm decreases gradually, indicating decreased AlcDH activity with the change of encapsulated  (Figures S11-S13). One week later, AlcDH/ NAD + @UiO-66-NH 2 -MNRs combined with Pt[(C 6 H 5 ) 3 P] 4 still remain comparable conversion in the reduction of pyruvic acid to lactic acid, in contrast to the activity of the fresh AlcDH/NAD + @UiO-66-NH 2 -MNR system ( Figure S14). The slight decrease in activity might be attributed to the falling of some UiO-66-NH 2 particles from the surface of MNRs, as confirmed by the SEM images, in which the smooth surface of the inner polymer layer can be observed ( Figure S15). Therefore, MOF-MNRs present an enhanced barrier with a good protective effect on AlcDH [4,48,49], indicating their great potential in effective encapsulation and separation protection. The other feature of MOF-MNRs is that certain MOFs with uniform micropores can control the molecular transport, in which only the molecules with smaller size than aperture size of MOFs can enter and contact with the enzyme while the bigger size molecules can not. Hence, one kind of metal complex catalysts with smaller size, platinum acetylacetonate (C 10 H 14 O 4 Pt) rather than Pt[(C 6 H 5 ) 3 P] 4 , was used to demonstrate the selective transport of MOF channel. When AlcDH/NAD + @UiO-66-NH 2 -MNRs are used as a biocatalyst, the conversion of concurrent chemo-biocatalysis decreases gradually after introducing smaller size C 10 H 14 O 4 Pt as chemocatalysts (Figure 3(c)). The MOFs as shell of MNRs can allow small-sized of metal complex catalysts to enter the inside of the MOF-MNRs as well as to denature the enzyme. The designed MOF-MNRs can not only protect enzyme against the metal catalyst deactivation but also ensure the occurrence of the concurrent chemo-biocascade catalysis in more complex reaction system, such as in the one with 6 Research protease and metal catalysts coexisting. Protease, one kind of enzyme, can induce the proteolysis of some enzymes (e.g., AlcDH) and decrease enzymatic activity. The AlcDH/ NAD + @UiO-66-NH 2 -MNRs are highly resistant to digestion by protease and retain the initial activity of AlcDH in concurrent chemo-biocatalysis, mainly due to the uniform micropore structure of UiO-66-NH 2 ( Figure S10). In the concurrent chemo-biocatalysis, MOF-MNRs not only demonstrate compartmentalization effect by the encapsulation and protection of biocatalysts but also display size selectivity of the substances and shorten the reaction distance and the mutual communication of the chemo-bioincompatible catalysts.  4 on the surface of UiO-66-NH 2 tends to be increased due to the electrostatic interaction (Figure 4(a)), as confirmed by the zeta potential (Table S1) and SEM mapping images ( Figure S16). The content of metal complex on the surface of the MOF-MNRs is about 2% (Figure 4(b)). Such enrichment facilitates reaction acceleration; (2)  The results suggest that the increased rate of chemical reactions matches the reaction rate of enzymes, improving the overall chemo-bioreactions. Therefore, MOF-MNRs play a crucial role in developing highly efficient, concurrent chemo-biocatalysis.

MOF-MNR for Asymmetric Reduction.
To verify that the enzymes encapsulated within MNR retain their chiral catalytic property, we further explored the asymmetric hydrogenation of benzyl acetone. Specifically, the Pt[(C 6 H 5 ) 3 P] 4 catalyzes the transfer hydrogenation of NAD + to NADH in the presence of formate as a hydride donor. AlcDH catalyzes the asymmetric hydrogenation of benzyl acetone in the presence of NADH. The asymmetric hydrogenation of benzyl acetone is promoted by a mixture of Pt[(C 6 H 5 ) 3 P] 4 -AlcDH/NAD + @MOF-MNRs in conjunction with NAD + and formate ( Table 1). The optimized reaction condition is in the PBS solution at 40°C for higher or lower temperatures would affect the activity of AlcDH. The products of (S) 4-phenyl-2-butanol are observed to attain 94.7% conversion and 87.8% ee after 20 h at 40°C by UiO-66-NH 2 -MNRs combining the Pt[(C 6 H 5 ) 3 P] 4 and AlcDH-NAD + . By contrast, the conversion is only 5.56% by directly mixing the Pt[(C 6 H 5 ) 3 P] 4 and AlcDH-NAD + due to mutual deactivation of chemo-biocatalysts. Meanwhile, the combination of AlcDH/NAD + @PMMA-MNRs and Pt[(C 6 H 5 ) 3 P] 4 as catalysts results in low conversion of 65.40% and high 97.25% ee, since PMMA as shell could not entirely block the entrance of the metal complex catalysts. The MOF-MNRs' features of compartmentalization effect, protection of enzyme, regulation of the chemocatalysts, and communication of substrates can improve the synergistic catalytic ability in the concurrent chemo-biocatalysis for producing asymmetric (S) 4-phenyl-2-butanol. Such strategy has the potential to be extended to other one-pot reactions under mild conditions for achieving compatibility between metal complex catalysts and enzymes.

Conclusions
The designed MOF-MNRs can regulate the compatibility of chemo-and biocatalysts with high catalytic activity in concurrent chemo-biocatalysis. Firstly, different kinds of enzymes can be encapsulated inside MOF-MNRs by assembling on the oil-water interface for avoiding the external interference of metal complex catalysts or even protease enzyme, and their activity can be improved by the chemical microenvironment of MOF-MNRs. Secondly, MOF-MNRs have achieved size selectivity of the chemocatalysts and controllable communications of reaction substrates that originate from well-defined micropore nature of MOFs. Thirdly, the activity of chemocatalysts (Pt[(C 6 H 5 ) 3 P] 4 ) is improved by the enrichment of Pt[(C 6 H 5 ) 3 P] 4 and regulation of electronic status on MOF-MNR surface, which can adapt to the reaction condition of enzymes at a relatively low temperature and aqueous solution. The design of combining AlcDH/NAD + @MOF-MNRs and Pt[(C 6 H 5 ) 3 P] 4 catalysts results in an increased efficiency in concurrent chemo-biocatalysis and good enantioselectivity during the asymmetric transfer hydrogenation process. We believe that such study can provide promising research avenues in concurrent chemo-biocatalysis, which is not limited to the combination of biocatalyst and homogeneous chemocatalyst but can be extended to the integration of biocatalysts with heterogeneous chemocatalysts.

Materials and Methods
4.1. Materials and Measurements. ZrCl 4 , NH 2 BDC, N,Ndimethylformamide (DMF), alcohol dehydrogenase (AlcDH), nicotinamide adenine dinucleotide (NAD + ), dodecane, protease, Span 80, metal complexes, and pyruvic acid were purchased from Sigma-Aldrich; benzoic acid and heptanoic anhydride were purchased from Tokyo Chemical Industry (TCI); 4-phenyl-2-butanol and benzyl acetone were purchased from Alfa; sodium formate was purchased from Macklin. These commercial reagents were used as received. Ultrapure water was obtained by our lab's ultrapure water machine (MZY-UR10V). SEM images were taken under 5 kV accelerating voltage using JEOL JSM-7600. Hitachi F-4600 fluorescence spectrometer was used to measure fluorescence data. UV absorption spectra were measured by SHIMADZU UV-1750. Hydrophobic modification data were carried out on a contact angle meter (KRUSS GmbH, DSA1005). The adsorption and desorption isotherms of nitrogen were analyzed by Brunauer-Emmett-Teller (BET). XRD patterns were recorded on a Rigaku (SC-XRD, XtaLAB mini II). Confocal fluorescence microscope data were carried out on ZEISS LSM880 confocal microscope system. The cata-lytic tests were analyzed by a high-performance liquid chromatography (HPLC) LC-20D.

Synthesis of UiO-66-NH 2 .
UiO-66-NH 2 NPs were prepared on the basis of Schaate's method [54] after revision. Firstly, ZrCl 4 (0.16 g, 0.68 mmol), 2-aminoterephthalic acid (0.124 g, 0.68 mmol), and benzoic acid (0.84 g, 6.86 mmol) were mixed in 40 mL DMF. After that, dissolve the solution in a glass vial and sonicate for 10 min to make it evenly dispersed, followed by putting it in an oven at 120°C to react for 24 h. Next, it was cooled to room temperature, centrifuged, and washed 6 times with DMF and ethanol and centrifuged and put into vacuum oven.

Posthydrophobic
Modification of UiO-66-NH 2 . We referred to Lohse et al.'s method for posthydrophobic processes [55]. After grinding UiO-66-NH 2 into powder, 100 mg of them was dispersed into 10 mL heptanoic anhydride. The sample was sonicated for 15 min and then stirred at 100°C for 15 min. After cooling to room temperature and being centrifuged at 10000 rpm for 5 min, it was washed with ethanol for 3 times and put into vacuum oven at 120°C.

Preparation of MOF-MNRs and PMMA-MNRs.
Briefly, MOF-MNRs were self-assembled from Pickering emulsions of water and oil phases by shear forces. The hydrophobically modified UiO-66-NH 2 NPs were dissolved in the oil phase of 4 mL dodecane, and 15 mg PMMA was dissolved in acetone and various substances in the aqueous phase. After that, the emulsion was sheared using a PowerGen 125 set Homogenizer Polytron homogenizer (T-701FBT10P) fitted with an 8 mm dispersing tool at 18000 rpm. At last, the MOF-MNRs were obtained by removing the acetone using rotary evaporator under room temperature. For PMMA-MNRs, the surfactant Span 80 (0.5 wt%) was dispersed in the oil phase (4 mL), PMMA in the water phase of acetone, and PMMA-MNRs were formed under the action of shearing force.

Encapsulation of AlcDH and NAD + inside MOF-MNRs.
During the preparation of MOF-MNRs, 10 mg of AlcDH (99 × 69 × 58 Å, Figure S18) and 10 mg of NAD + were dissolved in 100 μL of 0.1 M phosphate buffer solution (PBS), and 32 μL of each was added to 448μL of PMMA solution. After being shaken well and added to 4 mL of dodecane dispersion of UiO-66-NH 2 , the MOF-MNRs with water-inoil structure could be formed under the action of shear force. 4.6. Confocal Fluorescence Microscope Characterization of MOF-MNRs. AlcDH was labelled by FITC; NAD + was labelled by RB under dark conditions. After the labeling, the enzyme and NAD + were coated according to the method in 4.4 and centrifuged and washed with 50% ethanol for 6 times, and then, the liquid was dropped in a confocal dish for further use. Afterwards, fluorescence microscopy and z-axis scanning were performed at 488 nm and 543 nm.   Figure S18) (0.8 μmol), formate (0.1 M), and pyruvic acid (2 M), the whole system was put into thermostatic shaker at 40°C for 12 h. Subsequently, after centrifugation and cell crusher treatment, the reaction efficiency of AlcDH/NAD + @MOF-MNRs with metal complex in the reduction of pyruvic acid was later determined by a previously reported method, in which the extent of the reaction proceeds and the production of pyruvate is investigated by the intensity of the reduced coenzyme NADH.

Data Availability
All data needed to evaluate the conclusions in the paper are present in the paper and the Supplementary Materials. Additional data related to this paper may be requested from the authors.

Supplementary Materials
Supplementary 1. Figure S1: BET comparison of UiO-66-NH 2 before and after hydrophobic modification. Supplementary 2. Figure S2: X-ray diffraction data for the synthesized, modified, and assembled MOF-MNRs. Supplementary 3. Figure S3: SEM images of MOF-MNRs. Supplementary 4. Figure S4: Fluorescence images of MOF-MNRs entrapped with FITC labelled AlcDH and RB labeled NAD+. Supplementary 5. Figure S5: comparison of the catalytic efficiency of the whole cycle reaction and the two half reaction catalyzed by either metal complex or AlcDH. Supplementary 6. Recyclability of AlcDH/NAD + @MOF-MNRs for concurrent chemobiocatalysis in the reduction of pyruvic acid. Supplementary 7. Figure S7: SEM images of PMMA-MNRs obtained in the presence of surfactants. Supplementary 8. Figure S8: comparison of enzyme activity of AlcDH/NAD + @MOF-MNRs and AlcDH/NAD + @PMMA-MNRs after 12 h. Supplementary 9. Figure S9: Diffusion investigation of FITC labelled AlcDH inside MOF-MNRs and PMMA-MNRs. Supplementary 10. Figure S10: comparison of the fluorescence intensity of the generated NADH after exchanging the location of AlcDH and metal complex and in the presence of protease. Supplementary 11. Figure S11: comparison of the UV/Vis absorption of AlcDH between unencapsulated AlcDH/NAD+, AlcDH/NAD + @PMMA-MNRs, and AlcDH/NAD + @MOF-MNRs after the reactions. Supplementary 12. Figure S12: UV/Vis absorption of pure AlcDH within 50 h. Supplementary 13. Figure S13: UV/Vis absorption of AlcDH/NAD + @MOF-MNRs within 8 d. Supplementary 14. Figure S14: activities of the concurrent chemo-bioreactions of pyruvic acid to lactic acid immediately after fresh preparation of the catalysts (red line) and after storage together at room temperature for a time interval of one week (black line). Supplementary 15. Figure S15: SEM images of MOF-MNRs after storing at room temperature for a week. Supplementary 16. Figure