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文章數：87 |
 永心鳳茶價位會不會太高？》公益路美食街攻略｜10家熱門餐廳全紀錄 |
| 在地生活｜大台北 2026/04/21 10:35:05 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
身為一個熱愛美食、喜歡在城市裡挖掘驚喜的人，臺中公益路一直是我最常出沒的地方之一。這條路可說是「臺中人的美食戰場」，從精緻西餐到創意火鍋，從日式丼飯到義式早午餐，每走幾步，就會有完全不同的特色料理餐廳。 這次我特別花了一整個月，實際造訪了公益路上十間口碑不錯的餐廳。有的是網友熱推的打卡名店，也有隱藏在巷弄裡的小驚喜。我以環境氛圍、口味表現、價格CP值與再訪意願為基準，整理出這篇實測評比。希望能幫正在猶豫去哪裡吃飯的你，找到那一間「吃完會想再來」的餐廳。 評比標準與整理方向
這次我走訪的10家餐廳橫跨不同料理類型，從高質感牛排館到巷弄系早午餐，每一間都有自己獨特的風格。為了讓整體比較更客觀，我依照以下四大面向進行評比，並搭配實際用餐體驗來打分。
整體而言，我希望這份評比不只是「哪家好吃」，而是幫你在不同情境下（約會、家庭聚餐、朋友小聚、商業午餐）都能快速找到合適的選擇。畢竟，美食不只是味覺的滿足，更是一段段與朋友共享的生活記憶。 10間臺中公益路餐廳評比懶人包公益路向來是臺中人聚餐的首選地段，從火鍋、燒肉到中式料理與早午餐，每走幾步就有驚喜。以下是我實際造訪過的10間代表性餐廳清單，橫跨平價、創意、高級各路風格。
一頭牛日式燒肉｜炭香濃郁的和牛饗宴，約會聚餐首選
走在公益路上，很難不被 一頭牛日式燒肉 的木質外觀吸引。低調卻不失質感的門面，搭配昏黃燈光與暖色調的內裝，讓人一進門就感受到濃濃的日式職人氛圍。店內空間不大，但桌距規劃得宜，每桌皆設有獨立排煙設備，烤肉時完全不怕滿身油煙味。 餐點特色
一頭牛的靈魂，絕對是他們招牌的「三國和牛拼盤」。 用餐體驗整體節奏掌握得非常好。店員會在你剛想烤下一片肉時貼心遞上夾子、幫忙換烤網，讓人完全不用分心。整場用餐過程就像一場表演，從視覺、嗅覺到味覺都被滿足。 綜合評分
地址：408臺中市南屯區公益路二段162號電話：04-23206800 小結語一頭牛日式燒肉不僅是「吃肉的地方」，更像是一場五感盛宴。從進門那一刻到最後一道甜點，都能感受到他們對細節的用心。 TANG Zhan 湯棧｜文青系火鍋代表，麻香湯底與視覺美感並重
在公益路這條美食戰線上，TANG Zhan 湯棧 是讓人一眼就會想走進去的那一種。 餐點特色
湯棧最有名的當然是它的「麻香鍋」。 用餐體驗整體氛圍比一般火鍋店更有質感。 綜合評分
地址：408臺中市南屯區公益路二段248號電話：04-22580617 官網：https://www.facebook.com/TangZhan.tw/ 小結語TANG Zhan 湯棧 把傳統火鍋做出新的樣貌保留臺式鍋物的溫度，又結合現代風格與細節服務，讓吃鍋這件事變得更有品味。 如果你想找一間兼具「好吃、好拍、好放鬆」的火鍋店，湯棧會是公益路上最有風格的選擇之一。 NINI 尼尼臺中店｜明亮寬敞的義式早午餐天堂
如果說前兩間是肉食愛好者的天堂，那 NINI 尼尼臺中店 絕對是想放鬆、聊聊天的好地方。餐廳外觀以白色系與大片玻璃窗為主，陽光灑進室內，讓人一踏入就有種度假般的輕盈感。假日早午餐時段特別熱鬧，建議提早訂位。 餐點特色
NINI 的菜單融合義式與臺灣人口味，選擇多樣且份量十足。主打的 松露燉飯 濃郁卻不膩口，米芯保留微Q口感；而 香蒜海鮮義大利麵 則以新鮮白蝦、花枝與淡菜搭配微辣蒜香，口感層次豐富。 用餐體驗店內氣氛輕鬆不拘謹，無論是一個人帶電腦工作、或朋友聚餐，都能找到舒服角落。餐點上桌速度穩定，服務人員態度親切、補水與收盤都非常主動。整體節奏讓人覺得「時間變慢了」，很適合想遠離忙碌日常的人。 綜合評分
地址：40861臺中市南屯區公益路二段18號電話：04-23288498 小結語NINI 尼尼臺中店是一間能讓人放下手機、慢慢吃飯的餐廳。餐點不追求浮誇，而是以「剛剛好」的份量與風味，陪伴每個平凡午後。如果你在找一間能邊吃邊聊天、拍照也漂亮的早午餐店，NINI 會是你在公益路上最不費力的幸福選擇。 加分100%浜中特選昆布鍋物｜平價卻用心的湯頭系火鍋，家庭聚餐好選擇
在公益路這條高質感餐廳林立的戰場上，加分100%浜中特選昆布鍋物 走的是截然不同的路線。它沒有浮誇的裝潢、也沒有高價位的套餐，但靠著實在的湯頭與親切的服務，默默吸引許多回頭客。每到用餐時間，總能看到家庭或情侶三兩成群地圍著鍋邊聊天。 餐點特色
主打 北海道浜中昆布湯底，湯頭清澈卻不單薄，越煮越能喝出海藻與柴魚的自然香氣。 用餐體驗整體氛圍偏家庭取向，桌距寬敞、座位舒適，帶小孩來也不覺擁擠。店員態度親切，補湯、收盤都很勤快，給人一種「被照顧著」的安心感。 綜合評分
地址：403臺中市西區公益路288號電話：0910855180 小結語加分100%浜中特選昆布鍋物是一間「不浮誇、但會讓人想再訪」的火鍋店。它不追求豪華擺盤，而是用最簡單的湯頭與新鮮食材，傳遞出家常卻不平凡的溫度。 印月餐廳｜中式料理的藝術演繹，宴客與家庭聚會首選
說到臺中公益路的中式料理代表，印月餐廳 絕對是榜上有名。這間開業多年的餐廳以「中菜西吃」的概念聞名，把傳統中式料理以現代手法重新詮釋。從建築外觀到餐具擺設，每個細節都散發著低調的典雅氣息。 餐點特色
印月最令人印象深刻的是他們將傳統中菜融入創意手法。 用餐體驗服務方面完全對得起餐廳的高級定位。從入座、點餐到上菜節奏，都拿捏得恰如其分。每道菜都會有服務人員細心介紹食材與吃法，讓人感受到「被款待」的尊榮感。 綜合評分
地址：408臺中市南屯區公益路二段818號電話：0422511155 小結語印月餐廳是一間「不只吃飯，更像品味生活」的地方。 KoDō 和牛燒肉｜極致職人精神，專為儀式感與頂級味覺而生
若要形容 KoDō 和牛燒肉 的用餐體驗，一句話足以總結——「像在欣賞一場關於肉的表演」。 餐點特色
這裡主打 日本A5和牛冷藏肉，以「精切厚燒」的方式呈現。 用餐體驗KoDō 的最大特色是「儀式感」。 綜合評分
地址：403臺中市西區公益路260號電話：0423220312 官網：https://www.facebook.com/kodo2018/ 小結語KoDō 和牛燒肉不是日常餐廳，而是一場體驗。 永心鳳茶｜在茶香裡用餐的優雅時光，臺味早午餐的新詮釋
走進 永心鳳茶公益店，彷彿進入一間有氣質的茶館。 餐點特色
永心鳳茶的餐點結合中式靈魂與西式擺盤，無論是「炸雞腿飯」還是「紅玉紅茶拿鐵」，都能讓人感受到熟悉卻不平凡的味道。 用餐體驗店內服務人員態度溫和，對茶品介紹詳盡。上餐節奏剛好，不急不徐。 綜合評分
地址：40360臺中市西區公益路68號三樓(勤美誠品)電話：0423221118 小結語永心鳳茶讓人重新定義「臺味」。 三希樓｜老饕級江浙功夫菜，穩重又帶人情味的中式饗宴
位於公益路上的 三希樓 是許多臺中老饕的口袋名單。 餐點特色
三希樓的菜色以 江浙與港式料理 為主，兼顧傳統與現代風味。 用餐體驗三希樓的服務給人一種老派但貼心的感覺。 綜合評分
地址：408臺中市南屯區公益路二段95號電話：0423202322 官網：https://www.sanxilou.com.tw/ 小結語三希樓是一間「吃得出功夫」的餐廳。 一笈壽司｜低調奢華的無菜單日料，職人手藝詮釋旬味極致
在熱鬧的公益路上，一笈壽司 低調得幾乎不顯眼。 餐點特色
一笈壽司採 Omakase（無菜單料理） 形式，每一餐都由主廚根據當日食材設計。 用餐體驗整場用餐約90分鐘，節奏緩慢但沉穩。 綜合評分
地址：408臺中市南屯區公益路二段25號電話：0423206368 官網：https://www.facebook.com/YIJI.sushi/ 小結語一笈壽司是一間真正讓人「放慢呼吸」的餐廳。 茶六燒肉堂｜人氣爆棚的和牛燒肉聖地，肉香與幸福感同時滿分
若要票選公益路上「最難訂位」的餐廳，茶六燒肉堂 絕對名列前茅。 餐點特色
茶六主打 和牛燒肉套餐，價格約落在 $700–$1000 間，份量與品質兼具。 用餐體驗茶六的服務效率相當高。店員親切、換網勤快、補水速度快，整場用餐流程流暢無壓力。 綜合評分
地址：403臺中市西區公益路268號電話：0423281167 官網：https://inline.app/booking/-L93VSXuz8o86ahWDRg0:inline-live-karuizawa/-LUYUEIOYwa7GCUpAFWA 小結語茶六燒肉堂用「穩定品質＋輕奢氛圍」抓住了臺中年輕族群的心。 吃完10家公益路餐廳後的心得與結語吃完這十家餐廳後，臺中公益路不只是一條美食街，而是一段生活風景線。 有的餐廳講究細膩與儀式感，像 一頭牛日式燒肉 與 一笈壽司，讓人感受到食材最純粹的美好 有的則以親切與溫度打動人心，像 加分昆布鍋物、永心鳳茶，讓人明白吃飯不只是為了飽足，而是一種被照顧的幸福。 而像茶六燒肉堂、TANG Zhan 湯棧 這類人氣名店，則用穩定的品質與熱絡的氛圍，成為許多臺中人心中「想吃肉就去那裡」的代名詞。 這十家店，構成了公益路最動人的縮影 有華麗的，也有溫柔的；有傳統的，也有創新的。 每一家都在自己的風格裡發光，讓人吃到的不只是料理，而是一種生活的溫度與節奏。 對我而言，這不僅是一場美食旅程，更是一趟關於「臺中味道」的回憶之旅。 FAQ：關於臺中公益路美食常見問題Q1：公益路哪一區的餐廳最集中？ Q2：需要提前訂位嗎？ 最後的話若要用一句話形容這趟美食之旅，我會說： KoDō 和牛燒肉情侶來合適嗎？ 如果你也和我一樣喜歡用味蕾探索一座城市，那就把這篇公益路美食攻略收藏起來吧。一笈壽司需要訂位嗎？ 無論是約會、慶生、家庭聚餐，或只是想犒賞一下辛苦的自己——這條路上永遠會有一間剛剛好的餐廳在等你。一頭牛日式燒肉婚前派對適合嗎？ 下一餐，不妨從這10家開始。KoDō 和牛燒肉服務態度如何？ 打開手機、約上朋友，讓公益路成為你生活裡最容易抵達的小確幸。茶六燒肉堂包廂適合尾牙嗎？ 如果你有私心愛店，也歡迎留言分享，NINI 尼尼臺中店家庭聚餐合適嗎？ 你的推薦，可能讓我下一趟美食旅程變得更精彩。加分100%浜中特選昆布鍋物尾牙拍照效果好嗎？ Image showing artificial ovary, where in vitro-generated female germ cells (magenta) enter meiosis (yellow cells) to become oocytes with help from supporting cells (cyan). This process is 4-times more efficient when the X chromosome is correctly turned OFF and ON again during germ cell development. Credit: Dr. Jacqueline Severino/CRG Discovery of ‘yoyo’ mechanism could pave the way for generating artificial oocytes in the lab. A potential new diagnostic marker that predicts the successful and efficient development of mammalian egg cells has been identified by scientists at the Center for Genomic Regulation (CRG) in Barcelona. The discovery could pave the way for generating artificial oocytes in the laboratory, helping researchers study the causes and treatments of infertility disorders and test the impact of drugs and chemicals on women’s reproduction. The research will be published today (May 23, 2022) in The EMBO Journal. Humans have 23 pairs of chromosomes. Between males and females, 22 pairs are shared, with the 23rd pair being the sex chromosomes. Males have an X and a Y chromosome, while females have two X’s. This causes a potential problem for the female cellular machinery, as two active X chromosomes generate an overdose of gene products, which is fatal for developing embryos or leads to cancer in adult life. To avoid this scenario, female cells inactivate one X chromosome by turning off its genes and compacting it. Little is known about how X-chromosome inactivation affects the development of reproductive cells. In mammals, oocytes develop from germ cells, precursor cells that migrate from early embryonic tissue to the developing gonads. Germ cells then undergo meiosis, an important chromosomal rearrangement process, which is responsible for the genetic uniqueness of each individual germ cell. Germ cells mature and eventually turn into functional sperm or oocytes. To address this question, researchers at the Centre for Genomic Regulation (CRG) built an X-chromosome reporter system (XRep), a tool that allowed them to study how the chromosome shapeshifts over time during germ cell development in vitro. Image showing artificial ovary (left), where in vitro-generated female germ cells (magenta) enter meiosis (yellow cells) to become oocytes with the help of supporting cells (cyan). This process is four times more efficient when the X chromosome is correctly turned OFF and ON again during germ cell development. Also shown (top right) are oocytes at different maturation stages: from more immature on the left to more advanced on the right. Finally, the chromosomal organization during the meiosis process is shown (lower right) when germ cells become unique by reshuffling their genetic material. Credit: Dr. Jacqueline Severino/CRG Importance of X-Chromosome ‘Yoyo’ in Germ Cell Efficiency Using female mouse cells, the method revealed a carefully orchestrated act of X-chromosome ‘yoyo’. If one X chromosome is briefly inactivated and then reactivated, it results in germ cells being four times more efficient for entering meiosis and transforming into egg cells compared to germ cells that have never turned their X chromosome ‘off and on’ again. In comparison, germ cells that failed to inactivate the X chromosome in the first place or reactivated it too rapidly showed abnormal gene expression and cell differentiation patterns. The study also found that cells with two active X chromosomes divided faster and easily reverted into a state of pluripotency. According to the authors, these characteristics are similar to human germ cell tumors, which come from germ cells that got lost during their migration to the gonads or failed to differentiate properly once inside the testicles and ovaries. The researchers deduced that a correct X-chromosome inactivation and reactivation sequence is an indicator of normal germ cell differentiation. The research team notes that further studies will be needed to confirm whether an abnormal X-chromosome state is a diagnostic indicator, or whether it could be a causal factor responsible for the cell abnormality. Potential for Generating Artificial Human Oocytes “Our findings have important implications for reproductive research because XRep allows us to assess cellular X-chromosome status in real time, helping identify and isolate germ cells with a high success rate of turning into oocytes,” says Dr. Bernhard Payer, Group Leader at the CRG and senior author of the study. “Human oocytes have never been generated completely in vitro. Monitoring the X-chromosome state during in vitro germ cell differentiation might therefore be a way to optimize the protocol to produce high-quality human eggs in the lab. Human eggs for research are scarce and difficult to obtain because they are currently only available from egg donors and are mostly used for reproductive purposes. In vitro-generated human eggs could therefore provide an unlimited resource to study the causes and treatments of infertility disorders and as well to test the safety of drugs and chemicals for women’s reproduction,” concludes Dr. Payer. Dr. Moritz Bauer, co-first author of the study, adds: “Our results also highlight how we need specific tools to study female cells. The vast majority of studies are performed using male cells, leading to a gender gap in scientific knowledge. We, therefore, need to stop looking at female development through the lens of male cells, which will contribute to our understanding of sex-specific disease progressions.” Reference: “Controlled X-chromosome activation dynamics defines meiotic potential of female mouse in vitro germ cells” by Jacqueline Severino, Moritz Bauer, Tom Mattimoe, Niccolò Arecco, Luca Cozzuto, Patricia Lorden, Norio Hamada, Yoshiaki Nosaka, So I Nagaoka, Pauline Audergon, Antonio Tarruell, Holger Heyn, Katsuhiko Hayashi, Mitinori Saitou and Bernhard Payer, 23 May 2022, The EMBO Journal. DOI: 10.15252/embj.2021109457 This image shows comparisons among Peking Man, Maba, Jinniushan, Dali and Harbin crania (from left to right). Credit: Kai Geng A near-perfectly preserved ancient human fossil known as the Harbin cranium sits in the Geoscience Museum in Hebei GEO University. The largest of known Homo skulls, scientists now say this skull represents a newly discovered human species named Homo longi or “Dragon Man.” Their findings, appearing in three papers publishing today (June 25, 2021) in the journal The Innovation, suggest that the Homo longi lineage may be our closest relatives — and has the potential to reshape our understanding of human evolution. This image shows a reconstruction of Dragon Man in his habitat. Credit: Chuang Zhao “The Harbin fossil is one of the most complete human cranial fossils in the world,” says author Qiang Ji, a professor of paleontology of Hebei GEO University. “This fossil preserved many morphological details that are critical for understanding the evolution of the Homo genus and the origin of Homo sapiens.” The cranium was reportedly discovered in the 1930s in Harbin City in the Heilongjiang province of China. The massive skull could contain a brain comparable in size to that of modern humans, but it featured larger, almost square eye sockets, thick brow ridges, a wide mouth, and oversized teeth. While it shows typical archaic human features, the Harbin cranium presents a mosaic combination of primitive and derived characters setting itself apart from all the other previously-named Homo species,” says Ji, leading to its new species designation of Homo longi. Scientists believe the cranium came from a male individual, approximately 50 years old, living in a forested, floodplain environment as part of a small community. “Like Homo sapiens, they hunted mammals and birds, gathered fruits and vegetables, and perhaps even caught fish,” remarks author Xijun Ni, a professor of primatology and paleoanthropology at the Chinese Academy of Sciences and Hebei GEO University. Given that the Harbin individual was likely very large in size as well as the location where the skull was found, researchers suggest H. longi may have been adapted for harsh environments, allowing them to disperse throughout Asia. Using a series of geochemical analyses, Ji, Ni, and their team dated the Harbin fossil to at least 146,000 years, placing it in the Middle Pleistocene, a dynamic era of human species migration. They hypothesize that H. longi and H. sapiens could have encountered each other during this era. “We see multiple evolutionary lineages of Homo species and populations co-existing in Asia, Africa, and Europe during that time. So, if Homo sapiens indeed got to East Asia that early, they could have a chance to interact with H. longi, and since we don’t know when the Harbin group disappeared, there could have been later encounters as well,” says author Chris Stringer, a paleoanthropologist at the Nature History Museum in London. Looking farther back in time, the researchers also find that Homo longi is one of our closest hominin relatives, even more closely related to us than Neanderthals. “It is widely believed that the Neanderthal belongs to an extinct lineage that is the closest relative of our own species. However, our discovery suggests that the new lineage we identified that includes Homo longi is the actual sister group of H. sapiens,” says Ni. Their reconstruction of the human tree of life also suggests that the common ancestor we share with Neanderthals existed even further back in time. “The divergence time between H. sapiens and the Neanderthals may be even deeper in evolutionary history than generally believed, over one million years,” says Ni. If true, we likely diverged from Neanderthals roughly 400,000 years earlier than scientists had thought. The researchers say that findings gathered from the Harbin cranium have the potential to rewrite major elements of human evolution. Their analysis into the life history of Homo longi suggest they were strong, robust humans whose potential interactions with Homo sapiens may have shaped our history in turn. “Altogether, the Harbin cranium provides more evidence for us to understand Homo diversity and evolutionary relationships among these diverse Homo species and populations,” says Ni. “We found our long-lost sister lineage.” References: “Geochemical provenancing and direct dating of the Harbin archaic human cranium” by Qingfeng Shao, Junyi Ge, Qiang Ji, Jinhua Li, Wensheng Wu, Yannan Ji, Tao Zhan, Chi Zhang, Qiang Li, Rainer Grün, Chris Stringer and Xijun Ni, 25 June 2021, The Innovation. DOI: 10.1016/j.xinn.2021.100131 “Late Middle Pleistocene Harbin cranium represents a new Homo species” by Qiang Ji, Wensheng Wu, Yannan Ji, Qiang Li and Xijun Ni, 25 June 2021, The Innovation. DOI: 10.1016/j.xinn.2021.100132 “Massive cranium from Harbin in northeastern China establishes a new Middle Pleistocene human lineage” by Xijun Ni, Qiang Ji, Wensheng Wu, Qingfeng Shao, Yannan Ji, Chi Zhang, Lei Liang, Junyi Ge, Zhen Guo, Jinhua Li, Qiang Li, Rainer Grün and Chris Stringer, 25 June 2021, The Innovation. DOI: 10.1016/j.xinn.2021.100130 DNA valve controlling molecular processes along DNA. Credit: Thomas Gorochowski Scientists created DNA valves for controlling cellular processes, using nanopore sequencing for rapid development. This technology opens new avenues for gene regulation and genome editing. Scientists at the University of Bristol have developed new biological parts that are able to shape the flow of cellular processes along DNA. The work, now published in the journal Nature Communications, offers a fresh perspective on how information is encoded in DNA and new tools for building sustainable biotechnologies. Despite being invisible to the naked eye, microorganisms are integral for our survival. They operate using DNA, often referred to as the code of life. DNA encodes numerous tools that could be useful to us, but we currently lack a complete understanding of how to interpret DNA sequences. Challenges in Understanding Microbial DNA Matthew Tarnowski, first author and a PhD student in Bristol’s School of Biological Sciences, said: “Understanding the microbial world is tricky. While reading a microbe’s DNA with a sequencer gives us a window into the underlying code, you still need to read a lot of different DNA sequences to understand how it actually works. It’s a bit like trying to learn a new language, but from only a few small fragments of text.” To tackle this problem, the Bristol team focused on how the information encoded in DNA is read, and specifically, how the flow of cellular processes along DNA are controlled. These biological information flows orchestrate many of the core functions of a cell and an ability to shape them would offer a way to guide cellular behaviors. Inspiration from Nature for DNA Valves Taking inspiration from nature, where it is known that flows on DNA are often complex and interwoven, the team focused on how these flows could be regulated by creating “valves” to tune the flow from one region of DNA to another. Dr. Thomas Gorochowski, senior author and Royal Society University Research Fellow at the University of Bristol, said: “Similar to a valve that controls the rate that a liquid flows through a pipe, these valves shape the flow of molecular processes along DNA. These flows allow cells to make sense of the information stored in their genomes and the ability to control them enables us to reprogram their behaviors in useful ways.” Designing new biological parts can typically take a huge amount of time. To get around this problem, the team employed methods to enable the rapid assembly of many DNA parts in parallel and a sequencing technology based on ‘nanopores’ that allowed them to simultaneously measure how each part worked. Dr. Gorochowski added: “Harnessing the unique features of nanopore sequencing was the step needed to unlock our ability to effectively design the biological valves. Rather than separately building and testing a couple at a time, we could instead assemble and test thousands in a mixed pool, helping us pull apart their design rules and better understand how they work.” Applications and Future Directions The authors go on to further show how valves can be used for regulating other biological components in the cell, opening avenues to the future simultaneous control of many genes and complex editing of genomes. Looking forward, the team are currently considering how this technology could be used responsibly. Dr. Mario Pansera, distinguished researcher of the Post-Growth Innovation Lab at the University of Vigo, Spain, said: “Now that they have crafted these tools, a big question is how they can be used responsibly and equitably in the real world. Post-growth entrepreneurship offers useful approaches for imagining more deliberative and inclusive ways to put such technology at the service of people.” Reference: “Massively parallel characterization of engineered transcript isoforms using direct RNA sequencing” by Matthew J. Tarnowski and Thomas E. Gorochowski, 21 January 2022, Nature Communications. DOI: 10.1038/s41467-022-28074-5 This work was funded by the Royal Society, BBSRC/EPSRC Bristol Centre for Synthetic Biology (BrisSynBio) and EPSRC/BBSRC Synthetic Biology Centre for Doctoral Training (SynBioCDT) with support from the Bristol BioDesign Institute (BBI). RRG455KLJIEVEWWF |
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